-
1
-
-
84863693493
-
The zinc-finger domains of PARP1 cooperate to recognize DNA strand breaks
-
Ali AA, Timinszky G, Arribas-Bosacoma R, Kozlowski M, Hassa PO, Hassler M, Ladurner AG, Pearl LH, and Oliver AW (2012) The zinc-finger domains of PARP1 cooperate to recognize DNA strand breaks. Nat Struct Mol Biol 19:685-692.
-
(2012)
Nat Struct Mol Biol
, vol.19
, pp. 685-692
-
-
Ali, A.A.1
Timinszky, G.2
Arribas-Bosacoma, R.3
Kozlowski, M.4
Hassa, P.O.5
Hassler, M.6
Ladurner, A.G.7
Pearl, L.H.8
Oliver, A.W.9
-
2
-
-
0033580856
-
PARP-2, a novel mammalian DNA damage-dependent poly(ADP-ribose) polymerase
-
Amé JC, Rolli V, Schreiber V, Niedergang C, Apiou F, Decker P, Muller S, Höger T, Ménissier-de Murcia J, and de Murcia G (1999) PARP-2, a novel mammalian DNA damage-dependent poly(ADP-ribose) polymerase. J Biol Chem 274:17860-17868.
-
(1999)
J Biol Chem
, vol.274
, pp. 17860-17868
-
-
Amé, J.C.1
Rolli, V.2
Schreiber, V.3
Niedergang, C.4
Apiou, F.5
Decker, P.6
Muller, S.7
Höger, T.8
Ménissier-De Murcia, J.9
De Murcia, G.10
-
3
-
-
84907030375
-
Structural basis for the inhibition of poly(ADP-ribose) polymerases 1 and 2 by BMN 673, a potent inhibitor derived from dihydropyridophthalazinone
-
Aoyagi-Scharber M, Gardberg AS, Yip BK, Wang B, Shen Y, and Fitzpatrick PA (2014) Structural basis for the inhibition of poly(ADP-ribose) polymerases 1 and 2 by BMN 673, a potent inhibitor derived from dihydropyridophthalazinone. Acta Crystallogr F Struct Biol Commun 70:1143-1149.
-
(2014)
Acta Crystallogr F Struct Biol Commun
, vol.70
, pp. 1143-1149
-
-
Aoyagi-Scharber, M.1
Gardberg, A.S.2
Yip, B.K.3
Wang, B.4
Shen, Y.5
Fitzpatrick, P.A.6
-
4
-
-
49249119415
-
A synthetic lethal therapeutic approach: Poly(ADP) ribose polymerase inhibitors for the treatment of cancers deficient in DNA double-strand break repair
-
Ashworth A (2008) A synthetic lethal therapeutic approach: poly(ADP) ribose polymerase inhibitors for the treatment of cancers deficient in DNA double-strand break repair. J Clin Oncol 26:3785-3790.
-
(2008)
J Clin Oncol
, vol.26
, pp. 3785-3790
-
-
Ashworth, A.1
-
5
-
-
11244280890
-
Involvement of poly(ADP-ribose) polymerase-1 and XRCC1/DNA ligase III in an alternative route for DNA double-strand breaks rejoining
-
Audebert M, Salles B, and Calsou P (2004) Involvement of poly(ADP-ribose) polymerase-1 and XRCC1/DNA ligase III in an alternative route for DNA double-strand breaks rejoining. J Biol Chem 279:55117-55126.
-
(2004)
J Biol Chem
, vol.279
, pp. 55117-55126
-
-
Audebert, M.1
Salles, B.2
Calsou, P.3
-
6
-
-
0030031666
-
Crystal structure of diphtheria toxin bound to nicotinamide adenine dinucleotide
-
Bell CE and Eisenberg D (1996) Crystal structure of diphtheria toxin bound to nicotinamide adenine dinucleotide. Biochemistry 35:1137-1149.
-
(1996)
Biochemistry
, vol.35
, pp. 1137-1149
-
-
Bell, C.E.1
Eisenberg, D.2
-
7
-
-
0019321793
-
Poly(ADP-ribose) synthesis in vitro programmed by damaged DNA. A comparison of DNA molecules containing different types of strand breaks
-
Benjamin RC and Gill DM (1980) Poly(ADP-ribose) synthesis in vitro programmed by damaged DNA. A comparison of DNA molecules containing different types of strand breaks. J Biol Chem 255:10502-10508.
-
(1980)
J Biol Chem
, vol.255
, pp. 10502-10508
-
-
Benjamin, R.C.1
Gill, D.M.2
-
8
-
-
33750552551
-
Mechanisms of cellular resistance to camptothecins
-
Beretta GL, Perego P, and Zunino F (2006) Mechanisms of cellular resistance to camptothecins. Curr Med Chem 13:3291-3305.
-
(2006)
Curr Med Chem
, vol.13
, pp. 3291-3305
-
-
Beretta, G.L.1
Perego, P.2
Zunino, F.3
-
9
-
-
84877857730
-
PARP and CHK inhibitors interact to cause DNA damage and cell death in mammary carcinoma cells
-
Booth L, Cruickshanks N, Ridder T, Dai Y, Grant S, and Dent P (2013) PARP and CHK inhibitors interact to cause DNA damage and cell death in mammary carcinoma cells. Cancer Biol Ther 14:458-465.
-
(2013)
Cancer Biol Ther
, vol.14
, pp. 458-465
-
-
Booth, L.1
Cruickshanks, N.2
Ridder, T.3
Dai, Y.4
Grant, S.5
Dent, P.6
-
10
-
-
84893517261
-
Molecular pathways: How can BRCA-mutated tumors become resistant to PARP inhibitors?
-
Bouwman P and Jonkers J (2014) Molecular pathways: how can BRCA-mutated tumors become resistant to PARP inhibitors? Clin Cancer Res 20:540-547.
-
(2014)
Clin Cancer Res
, vol.20
, pp. 540-547
-
-
Bouwman, P.1
Jonkers, J.2
-
11
-
-
0035137364
-
Differential effects of the poly (ADP-ribose) polymerase (PARP) inhibitor NU1025 on topoisomerase I and II inhibitor cytotoxicity in L1210 cells in vitro
-
Bowman KJ, Newell DR, Calvert AH, and Curtin NJ (2001) Differential effects of the poly (ADP-ribose) polymerase (PARP) inhibitor NU1025 on topoisomerase I and II inhibitor cytotoxicity in L1210 cells in vitro. Br J Cancer 84:106-112.
-
(2001)
Br J Cancer
, vol.84
, pp. 106-112
-
-
Bowman, K.J.1
Newell, D.R.2
Calvert, A.H.3
Curtin, N.J.4
-
12
-
-
33645532464
-
Inhibition of poly (ADP-ribose) polymerase activates ATM which is required for subsequent homologous recombination repair
-
Bryant HE and Helleday T (2006) Inhibition of poly (ADP-ribose) polymerase activates ATM which is required for subsequent homologous recombination repair. Nucleic Acids Res 34:1685-1691.
-
(2006)
Nucleic Acids Res
, vol.34
, pp. 1685-1691
-
-
Bryant, H.E.1
Helleday, T.2
-
13
-
-
17244375049
-
Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase
-
Bryant HE, Schultz N, Thomas HD, Parker KM, Flower D, Lopez E, Kyle S, Meuth M, Curtin NJ, and Helleday T (2005) Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase. Nature 434:913-917.
-
(2005)
Nature
, vol.434
, pp. 913-917
-
-
Bryant, H.E.1
Schultz, N.2
Thomas, H.D.3
Parker, K.M.4
Flower, D.5
Lopez, E.6
Kyle, S.7
Meuth, M.8
Curtin, N.J.9
Helleday, T.10
-
14
-
-
47949130625
-
Topoisomerase levels determine chemotherapy response in vitro and in vivo
-
Burgess DJ, Doles J, Zender L, Xue W, Ma B, McCombie WR, Hannon GJ, Lowe SW, and Hemann MT (2008) Topoisomerase levels determine chemotherapy response in vitro and in vivo. Proc Natl Acad Sci USA 105:9053-9058.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 9053-9058
-
-
Burgess, D.J.1
Doles, J.2
Zender, L.3
Xue, W.4
Ma, B.5
McCombie, W.R.6
Hannon, G.J.7
Lowe, S.W.8
Hemann, M.T.9
-
15
-
-
10744226451
-
Anticancer chemosensitization and radiosensitization by the novel poly(ADP-ribose) polymerase-1 inhibitor AG14361
-
Calabrese CR, Almassy R, Barton S, Batey MA, Calvert AH, Canan-Koch S, Durkacz BW, Hostomsky Z, Kumpf RA, Kyle S, et al. (2004) Anticancer chemosensitization and radiosensitization by the novel poly(ADP-ribose) polymerase-1 inhibitor AG14361. J Natl Cancer Inst 96:56-67.
-
(2004)
J Natl Cancer Inst
, vol.96
, pp. 56-67
-
-
Calabrese, C.R.1
Almassy, R.2
Barton, S.3
Batey, M.A.4
Calvert, A.H.5
Canan-Koch, S.6
Durkacz, B.W.7
Hostomsky, Z.8
Kumpf, R.A.9
Kyle, S.10
-
16
-
-
84888096960
-
Proteomic markers of DNA repair and PI3K pathway activation predict response to the PARP inhibitor BMN 673 in small cell lung cancer
-
Cardnell RJ, Feng Y, Diao L, Fan YH, Masrorpour F, Wang J, Shen Y, Mills GB, Minna JD, Heymach JV, et al. (2013) Proteomic markers of DNA repair and PI3K pathway activation predict response to the PARP inhibitor BMN 673 in small cell lung cancer. Clin Cancer Res 19:6322-6328.
-
(2013)
Clin Cancer Res
, vol.19
, pp. 6322-6328
-
-
Cardnell, R.J.1
Feng, Y.2
Diao, L.3
Fan, Y.H.4
Masrorpour, F.5
Wang, J.6
Shen, Y.7
Mills, G.B.8
Minna, J.D.9
Heymach, J.V.10
-
17
-
-
2342507720
-
AP endonuclease and poly(ADP-ribose) polymerase-1 interact with the same base excision repair intermediate
-
Cistulli C, Lavrik OI, Prasad R, Hou E, and Wilson SH (2004) AP endonuclease and poly(ADP-ribose) polymerase-1 interact with the same base excision repair intermediate. DNA Repair (Amst) 3:581-591.
-
(2004)
DNA Repair (Amst)
, vol.3
, pp. 581-591
-
-
Cistulli, C.1
Lavrik, O.I.2
Prasad, R.3
Hou, E.4
Wilson, S.H.5
-
18
-
-
84870218588
-
DNA repair dysregulation from cancer driver to therapeutic target
-
Curtin NJ (2012) DNA repair dysregulation from cancer driver to therapeutic target. Nat Rev Cancer 12:801-817.
-
(2012)
Nat Rev Cancer
, vol.12
, pp. 801-817
-
-
Curtin, N.J.1
-
19
-
-
84886717487
-
Therapeutic applications of PARP inhibitors: Anticancer therapy and beyond
-
Curtin NJ and Szabo C (2013) Therapeutic applications of PARP inhibitors: anticancer therapy and beyond. Mol Aspects Med 34:1217-1256.
-
(2013)
Mol Aspects Med
, vol.34
, pp. 1217-1256
-
-
Curtin, N.J.1
Szabo, C.2
-
20
-
-
84898978631
-
PARP1-TDP1 coupling for the repair of topoisomerase I-induced DNA damage
-
Das BB, Huang SY, Murai J, Rehman I, Amé JC, Sengupta S, Das SK, Majumdar P, Zhang H, Biard D, et al. (2014) PARP1-TDP1 coupling for the repair of topoisomerase I-induced DNA damage. Nucleic Acids Res 42:4435-4449.
-
(2014)
Nucleic Acids Res
, vol.42
, pp. 4435-4449
-
-
Das, B.B.1
Huang, S.Y.2
Murai, J.3
Rehman, I.4
Amé, J.C.5
Sengupta, S.6
Das, S.K.7
Majumdar, P.8
Zhang, H.9
Biard, D.10
-
21
-
-
0033941729
-
Potentiation of temozolomide and topotecan growth inhibition and cytotoxicity by novel poly(adenosine diphosphoribose) polymerase inhibitors in a panel of human tumor cell lines
-
Delaney CA, Wang LZ, Kyle S, White AW, Calvert AH, Curtin NJ, Durkacz BW, Hostomsky Z, and Newell DR (2000) Potentiation of temozolomide and topotecan growth inhibition and cytotoxicity by novel poly(adenosine diphosphoribose) polymerase inhibitors in a panel of human tumor cell lines. Clin Cancer Res 6: 2860-2867.
-
(2000)
Clin Cancer Res
, vol.6
, pp. 2860-2867
-
-
Delaney, C.A.1
Wang, L.Z.2
Kyle, S.3
White, A.W.4
Calvert, A.H.5
Curtin, N.J.6
Durkacz, B.W.7
Hostomsky, Z.8
Newell, D.R.9
-
22
-
-
0018906390
-
(ADP-ribose)n participates in DNA excision repair
-
Durkacz BW, Omidiji O, Gray DA, and Shall S (1980) (ADP-ribose)n participates in DNA excision repair. Nature 283:593-596.
-
(1980)
Nature
, vol.283
, pp. 593-596
-
-
Durkacz, B.W.1
Omidiji, O.2
Gray, D.A.3
Shall, S.4
-
23
-
-
84880329307
-
PARP inhibitors: Polypharmacology versus selective inhibition
-
Ekblad T, Camaioni E, Schüler H, and Macchiarulo A (2013) PARP inhibitors: polypharmacology versus selective inhibition. FEBS J 280:3563-3575.
-
(2013)
FEBS J
, vol.280
, pp. 3563-3575
-
-
Ekblad, T.1
Camaioni, E.2
Schüler, H.3
Macchiarulo, A.4
-
24
-
-
0024229066
-
Evidence that DNA topoisomerase I is necessary for the cytotoxic effects of camptothecin
-
Eng WK, Faucette L, Johnson RK, and Sternglanz R (1988) Evidence that DNA topoisomerase I is necessary for the cytotoxic effects of camptothecin. Mol Pharmacol 34:755-760.
-
(1988)
Mol Pharmacol
, vol.34
, pp. 755-760
-
-
Eng, W.K.1
Faucette, L.2
Johnson, R.K.3
Sternglanz, R.4
-
25
-
-
17244373777
-
Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy
-
Farmer H, McCabe N, Lord CJ, Tutt AN, Johnson DA, Richardson TB, Santarosa M, Dillon KJ, Hickson I, Knights C, et al. (2005) Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy. Nature 434:917-921.
-
(2005)
Nature
, vol.434
, pp. 917-921
-
-
Farmer, H.1
McCabe, N.2
Lord, C.J.3
Tutt, A.N.4
Johnson, D.A.5
Richardson, T.B.6
Santarosa, M.7
Dillon, K.J.8
Hickson, I.9
Knights, C.10
-
26
-
-
84941590233
-
Talazoparib (BMN-673) as single agent and in combination with temozolomide or PI3K pathway inhibitors in small cell lung cancer and gastric cancer models
-
2014 Nov 18-21; Barcelona, Spain
-
Feng Y, Shen Y, and Wang E (2014) Talazoparib (BMN-673) as single agent and in combination with temozolomide or PI3K pathway inhibitors in small cell lung cancer and gastric cancer models. 26th EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics; 2014 Nov 18-21; Barcelona, Spain.
-
(2014)
26th EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics
-
-
Feng, Y.1
Shen, Y.2
Wang, E.3
-
27
-
-
77953764486
-
Evolution of poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors. From concept to clinic
-
Ferraris DV (2010) Evolution of poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors. From concept to clinic. J Med Chem 53:4561-4584.
-
(2010)
J Med Chem
, vol.53
, pp. 4561-4584
-
-
Ferraris, D.V.1
-
28
-
-
77954032829
-
Poly(ADP)-ribose polymerase inhibition: Frequent durable responses in BRCA carrier ovarian cancer correlating with platinum-free interval
-
Fong PC, Yap TA, Boss DS, Carden CP, Mergui-Roelvink M, Gourley C, De Greve J, Lubinski J, Shanley S, Messiou C, et al. (2010) Poly(ADP)-ribose polymerase inhibition: frequent durable responses in BRCA carrier ovarian cancer correlating with platinum-free interval. J Clin Oncol 28:2512-2519.
-
(2010)
J Clin Oncol
, vol.28
, pp. 2512-2519
-
-
Fong, P.C.1
Yap, T.A.2
Boss, D.S.3
Carden, C.P.4
Mergui-Roelvink, M.5
Gourley, C.6
De Greve, J.7
Lubinski, J.8
Shanley, S.9
Messiou, C.10
-
29
-
-
74049112025
-
Discovery and SAR of substituted 3-oxoisoindoline-4-carboxamides as potent inhibitors of poly(ADP-ribose) polymerase (PARP) for the treatment of cancer
-
Gandhi VB, Luo Y, Liu X, Shi Y, Klinghofer V, Johnson EF, Park C, Giranda VL, Penning TD, and Zhu GD (2010) Discovery and SAR of substituted 3-oxoisoindoline-4-carboxamides as potent inhibitors of poly(ADP-ribose) polymerase (PARP) for the treatment of cancer. Bioorg Med Chem Lett 20:1023-1026.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 1023-1026
-
-
Gandhi, V.B.1
Luo, Y.2
Liu, X.3
Shi, Y.4
Klinghofer, V.5
Johnson, E.F.6
Park, C.7
Giranda, V.L.8
Penning, T.D.9
Zhu, G.D.10
-
30
-
-
84880586264
-
Discovery of novel benzo[b][1,4] oxazin-3(4H)-ones as poly(ADP-ribose)polymerase inhibitors
-
Gangloff AR, Brown J, de Jong R, Dougan DR, Grimshaw CE, Hixon M, Jennings A, Kamran R, Kiryanov A, O'Connell S, et al. (2013) Discovery of novel benzo[b][1,4] oxazin-3(4H)-ones as poly(ADP-ribose)polymerase inhibitors. Bioorg Med Chem Lett 23:4501-4505.
-
(2013)
Bioorg Med Chem Lett
, vol.23
, pp. 4501-4505
-
-
Gangloff, A.R.1
Brown, J.2
De Jong, R.3
Dougan, D.R.4
Grimshaw, C.E.5
Hixon, M.6
Jennings, A.7
Kamran, R.8
Kiryanov, A.9
O'Connell, S.10
-
31
-
-
84929056250
-
Poly(ADP-ribose) polymerase 1 (PARP1) overexpression in human breast cancer stem cells and resistance to olaparib
-
Gilabert M, Launay S, Ginestier C, Bertucci F, Audebert S, Pophillat M, Toiron Y, Baudelet E, Finetti P, Noguchi T, et al. (2014) Poly(ADP-ribose) polymerase 1 (PARP1) overexpression in human breast cancer stem cells and resistance to olaparib. PLoS One 9:e104302.
-
(2014)
PLoS One
, vol.9
-
-
Gilabert, M.1
Launay, S.2
Ginestier, C.3
Bertucci, F.4
Audebert, S.5
Pophillat, M.6
Toiron, Y.7
Baudelet, E.8
Finetti, P.9
Noguchi, T.10
-
32
-
-
77954374334
-
Poly(ADP-ribose) polymerase is hyperactivated in homologous recombination-defective cells
-
Gottipati P, Vischioni B, Schultz N, Solomons J, Bryant HE, Djureinovic T, Issaeva N, Sleeth K, Sharma RA, and Helleday T (2010) Poly(ADP-ribose) polymerase is hyperactivated in homologous recombination-defective cells. Cancer Res 70:5389-5398.
-
(2010)
Cancer Res
, vol.70
, pp. 5389-5398
-
-
Gottipati, P.1
Vischioni, B.2
Schultz, N.3
Solomons, J.4
Bryant, H.E.5
Djureinovic, T.6
Issaeva, N.7
Sleeth, K.8
Sharma, R.A.9
Helleday, T.10
-
33
-
-
84906217436
-
Histone deacetylase inhibitor treatment induces 'BRCAness' and synergistic lethality with PARP inhibitor and cisplatin against human triple negative breast cancer cells
-
Ha K, Fiskus W, Choi DS, Bhaskara S, Cerchietti L, Devaraj SG, Shah B, Sharma S, Chang JC, Melnick AM, et al. (2014) Histone deacetylase inhibitor treatment induces 'BRCAness' and synergistic lethality with PARP inhibitor and cisplatin against human triple negative breast cancer cells. Oncotarget 5:5637-5650.
-
(2014)
Oncotarget
, vol.5
, pp. 5637-5650
-
-
Ha, K.1
Fiskus, W.2
Choi, D.S.3
Bhaskara, S.4
Cerchietti, L.5
Devaraj, S.G.6
Shah, B.7
Sharma, S.8
Chang, J.C.9
Melnick, A.M.10
-
34
-
-
38149057387
-
PARP1-dependent kinetics of recruitment of MRE11 and NBS1 proteins to multiple DNA damage sites
-
Haince JF, McDonald D, Rodrigue A, Déry U, Masson JY, Hendzel MJ, and Poirier GG (2008) PARP1-dependent kinetics of recruitment of MRE11 and NBS1 proteins to multiple DNA damage sites. J Biol Chem 283:1197-1208.
-
(2008)
J Biol Chem
, vol.283
, pp. 1197-1208
-
-
Haince, J.F.1
McDonald, D.2
Rodrigue, A.3
Déry, U.4
Masson, J.Y.5
Hendzel, M.J.6
Poirier, G.G.7
-
35
-
-
84870392591
-
Towards a structural understanding of PARP1 activation and related signalling ADP-ribosyl-transferases
-
Hassler M and Ladurner AG (2012) Towards a structural understanding of PARP1 activation and related signalling ADP-ribosyl-transferases. Curr Opin Struct Biol 22:721-729.
-
(2012)
Curr Opin Struct Biol
, vol.22
, pp. 721-729
-
-
Hassler, M.1
Ladurner, A.G.2
-
36
-
-
3843071128
-
Rational approaches to discovery of orally active and brain-penetrable quinazolinone inhibitors of poly(ADP-ribose) polymerase
-
Hattori K, Kido Y, Yamamoto H, Ishida J, Kamijo K, Murano K, Ohkubo M, Kinoshita T, Iwashita A, Mihara K, et al. (2004) Rational approaches to discovery of orally active and brain-penetrable quinazolinone inhibitors of poly(ADP-ribose) polymerase. J Med Chem 47:4151-4154.
-
(2004)
J Med Chem
, vol.47
, pp. 4151-4154
-
-
Hattori, K.1
Kido, Y.2
Yamamoto, H.3
Ishida, J.4
Kamijo, K.5
Murano, K.6
Ohkubo, M.7
Kinoshita, T.8
Iwashita, A.9
Mihara, K.10
-
37
-
-
80052168685
-
The underlying mechanism for the PARP and BRCA synthetic lethality: Clearing up the misunderstandings
-
Helleday T (2011) The underlying mechanism for the PARP and BRCA synthetic lethality: clearing up the misunderstandings. Mol Oncol 5:387-393.
-
(2011)
Mol Oncol
, vol.5
, pp. 387-393
-
-
Helleday, T.1
-
38
-
-
84941570950
-
PARP inhibitors trap PARP1 onto damaged DNA via catalytic inhibition and not by an allosteric mechanism (Abstract)
-
Hopkins T, Solomon L, Shi YH, Rodriguez L, Donawho C, DiGiammorino E, Panchal S, Olson A, Stolarik D, Osterling D, et al. (2014) PARP inhibitors trap PARP1 onto damaged DNA via catalytic inhibition and not by an allosteric mechanism (Abstract). Eur J Cancer 50:82-83.
-
(2014)
Eur J Cancer
, vol.50
, pp. 82-83
-
-
Hopkins, T.1
Solomon, L.2
Shi, Y.H.3
Rodriguez, L.4
Donawho, C.5
DiGiammorino, E.6
Panchal, S.7
Olson, A.8
Stolarik, D.9
Osterling, D.10
-
39
-
-
18144413027
-
Poly(ADP-ribose) polymerase activity prevents signaling pathways for cell cycle arrest after DNA methylating agent exposure
-
Horton JK, Stefanick DF, Naron JM, Kedar PS, and Wilson SH (2005) Poly(ADP-ribose) polymerase activity prevents signaling pathways for cell cycle arrest after DNA methylating agent exposure. J Biol Chem 280:15773-15785.
-
(2005)
J Biol Chem
, vol.280
, pp. 15773-15785
-
-
Horton, J.K.1
Stefanick, D.F.2
Naron, J.M.3
Kedar, P.S.4
Wilson, S.H.5
-
40
-
-
84905975773
-
Base excision repair defects invoke hypersensitivity to PARP inhibition
-
Horton JK, Stefanick DF, Prasad R, Gassman NR, Kedar PS, and Wilson SH (2014) Base excision repair defects invoke hypersensitivity to PARP inhibition. Mol Cancer Res 12:1128-1139.
-
(2014)
Mol Cancer Res
, vol.12
, pp. 1128-1139
-
-
Horton, J.K.1
Stefanick, D.F.2
Prasad, R.3
Gassman, N.R.4
Kedar, P.S.5
Wilson, S.H.6
-
41
-
-
84873054943
-
Predicting enhanced cell killing through PARP inhibition
-
Horton JK and Wilson SH (2013a) Predicting enhanced cell killing through PARP inhibition. Mol Cancer Res 11:13-18.
-
(2013)
Mol Cancer Res
, vol.11
, pp. 13-18
-
-
Horton, J.K.1
Wilson, S.H.2
-
42
-
-
84891046100
-
Strategic combination of DNA-damaging agent and PARP inhibitor results in enhanced cytotoxicity
-
Horton JK and Wilson SH (2013b) Strategic combination of DNA-damaging agent and PARP inhibitor results in enhanced cytotoxicity. Front Oncol 3:257.
-
(2013)
Front Oncol
, vol.3
, pp. 257
-
-
Horton, J.K.1
Wilson, S.H.2
-
43
-
-
22744438407
-
Synthesis and mechanism of action studies of a series of norindenoisoquinoline topoisomerase I poisons reveal an inhibitor with a flipped orientation in the ternary DNA-enzyme-inhibitor complex as determined by X-ray crystallographic analysis
-
Ioanoviciu A, Antony S, Pommier Y, Staker BL, Stewart L, and Cushman M (2005) Synthesis and mechanism of action studies of a series of norindenoisoquinoline topoisomerase I poisons reveal an inhibitor with a flipped orientation in the ternary DNA-enzyme-inhibitor complex as determined by X-ray crystallographic analysis. J Med Chem 48:4803-4814.
-
(2005)
J Med Chem
, vol.48
, pp. 4803-4814
-
-
Ioanoviciu, A.1
Antony, S.2
Pommier, Y.3
Staker, B.L.4
Stewart, L.5
Cushman, M.6
-
44
-
-
20044393463
-
Discovery of quinazolinone and quinoxaline derivatives as potent and selective poly(ADP-ribose) polymerase-1/2 inhibitors
-
Iwashita A, Hattori K, Yamamoto H, Ishida J, Kido Y, Kamijo K, Murano K, Miyake H, Kinoshita T, Warizaya M, et al. (2005) Discovery of quinazolinone and quinoxaline derivatives as potent and selective poly(ADP-ribose) polymerase-1/2 inhibitors. FEBS Lett 579:1389-1393.
-
(2005)
FEBS Lett
, vol.579
, pp. 1389-1393
-
-
Iwashita, A.1
Hattori, K.2
Yamamoto, H.3
Ishida, J.4
Kido, Y.5
Kamijo, K.6
Murano, K.7
Miyake, H.8
Kinoshita, T.9
Warizaya, M.10
-
45
-
-
79960150694
-
Compromised CDK1 activity sensitizes BRCA-proficient cancers to PARP inhibition
-
Johnson N, Li YC, Walton ZE, Cheng KA, Li D, Rodig SJ, Moreau LA, Unitt C, Bronson RT, Thomas HD, et al. (2011) Compromised CDK1 activity sensitizes BRCA-proficient cancers to PARP inhibition. Nat Med 17:875-882.
-
(2011)
Nat Med
, vol.17
, pp. 875-882
-
-
Johnson, N.1
Li, Y.C.2
Walton, Z.E.3
Cheng, K.A.4
Li, D.5
Rodig, S.J.6
Moreau, L.A.7
Unitt, C.8
Bronson, R.T.9
Thomas, H.D.10
-
46
-
-
0018723423
-
Poly(ADP-ribose) levels in carcinogen-treated cells
-
Juarez-Salinas H, Sims JL, and Jacobson MK (1979) Poly(ADP-ribose) levels in carcinogen-treated cells. Nature 282:740-741.
-
(1979)
Nature
, vol.282
, pp. 740-741
-
-
Juarez-Salinas, H.1
Sims, J.L.2
Jacobson, M.K.3
-
47
-
-
84858597564
-
Increased PARP-1 association with DNA in alkylation damaged, PARP-inhibited mouse fibroblasts
-
Kedar PS, Stefanick DF, Horton JK, and Wilson SH (2012) Increased PARP-1 association with DNA in alkylation damaged, PARP-inhibited mouse fibroblasts. Mol Cancer Res 10:360-368.
-
(2012)
Mol Cancer Res
, vol.10
, pp. 360-368
-
-
Kedar, P.S.1
Stefanick, D.F.2
Horton, J.K.3
Wilson, S.H.4
-
48
-
-
0346725042
-
Inhibitor-induced structural change of the active site of human poly(ADP-ribose) polymerase
-
Kinoshita T, Nakanishi I, Warizaya M, Iwashita A, Kido Y, Hattori K, and Fujii T (2004) Inhibitor-induced structural change of the active site of human poly(ADP-ribose) polymerase. FEBS Lett 556:43-46.
-
(2004)
FEBS Lett
, vol.556
, pp. 43-46
-
-
Kinoshita, T.1
Nakanishi, I.2
Warizaya, M.3
Iwashita, A.4
Kido, Y.5
Hattori, K.6
Fujii, T.7
-
49
-
-
77954274504
-
The PARP side of the nucleus: Molecular actions, physiological outcomes, and clinical targets
-
Krishnakumar R and Kraus WL (2010) The PARP side of the nucleus: molecular actions, physiological outcomes, and clinical targets. Mol Cell 39:8-24.
-
(2010)
Mol Cell
, vol.39
, pp. 8-24
-
-
Krishnakumar, R.1
Kraus, W.L.2
-
50
-
-
84873524967
-
PARP-1 mechanism for coupling DNA damage detection to poly(ADP-ribose) synthesis
-
Langelier MF and Pascal JM (2013) PARP-1 mechanism for coupling DNA damage detection to poly(ADP-ribose) synthesis. Curr Opin Struct Biol 23:134-143.
-
(2013)
Curr Opin Struct Biol
, vol.23
, pp. 134-143
-
-
Langelier, M.F.1
Pascal, J.M.2
-
51
-
-
79953176276
-
Crystal structures of poly (ADP-ribose) polymerase-1 (PARP-1) zinc fingers bound to DNA: Structural and functional insights into DNA-dependent PARP-1 activity
-
Langelier MF, Planck JL, Roy S, and Pascal JM (2011) Crystal structures of poly (ADP-ribose) polymerase-1 (PARP-1) zinc fingers bound to DNA: structural and functional insights into DNA-dependent PARP-1 activity. J Biol Chem 286: 10690-10701.
-
(2011)
J Biol Chem
, vol.286
, pp. 10690-10701
-
-
Langelier, M.F.1
Planck, J.L.2
Roy, S.3
Pascal, J.M.4
-
52
-
-
84860806404
-
Structural basis for DNA damage-dependent poly(ADP-ribosyl)ation by human PARP-1
-
Langelier MF, Planck JL, Roy S, and Pascal JM (2012) Structural basis for DNA damage-dependent poly(ADP-ribosyl)ation by human PARP-1. Science 336: 728-732.
-
(2012)
Science
, vol.336
, pp. 728-732
-
-
Langelier, M.F.1
Planck, J.L.2
Roy, S.3
Pascal, J.M.4
-
53
-
-
41549108573
-
A third zinc-binding domain of human poly(ADP-ribose) polymerase-1 coordinates DNA-dependent enzyme activation
-
Langelier MF, Servent KM, Rogers EE, and Pascal JM (2008) A third zinc-binding domain of human poly(ADP-ribose) polymerase-1 coordinates DNA-dependent enzyme activation. J Biol Chem 283:4105-4114.
-
(2008)
J Biol Chem
, vol.283
, pp. 4105-4114
-
-
Langelier, M.F.1
Servent, K.M.2
Rogers, E.E.3
Pascal, J.M.4
-
54
-
-
79960015997
-
Identification of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies
-
Lehmann BD, Bauer JA, Chen X, Sanders ME, Chakravarthy AB, Shyr Y, and Pietenpol JA (2011) Identification of human triple-negative breast cancer subtypes and preclinical models for selection of targeted therapies. J Clin Invest 121:2750-2767.
-
(2011)
J Clin Invest
, vol.121
, pp. 2750-2767
-
-
Lehmann, B.D.1
Bauer, J.A.2
Chen, X.3
Sanders, M.E.4
Chakravarthy, A.B.5
Shyr, Y.6
Pietenpol, J.A.7
-
55
-
-
0027278557
-
Instability and decay of the primary structure of DNA
-
Lindahl T (1993) Instability and decay of the primary structure of DNA. Nature 362: 709-715.
-
(1993)
Nature
, vol.362
, pp. 709-715
-
-
Lindahl, T.1
-
56
-
-
84882762748
-
PARP inhibitor with selectivity toward ADP-ribosytransferase ARTD3/PARP3
-
Lindgren AE, Karlberg T, Thorsell AG, Hesse M, Spjut S, Ekblad T, Andersson CD, Pinto AF, Weigelt J, Hottiger MO, et al. (2013) PARP inhibitor with selectivity toward ADP-ribosytransferase ARTD3/PARP3. ACS Chem Biol 8:1698-1703.
-
(2013)
ACS Chem Biol
, vol.8
, pp. 1698-1703
-
-
Lindgren, A.E.1
Karlberg, T.2
Thorsell, A.G.3
Hesse, M.4
Spjut, S.5
Ekblad, T.6
Andersson, C.D.7
Pinto, A.F.8
Weigelt, J.9
Hottiger, M.O.10
-
57
-
-
72449148827
-
Acquired resistance to combination treatment with temozolomide and ABT-888 is mediated by both base excision repair and homologous recombination DNA repair pathways
-
Liu X, Han EK, Anderson M, Shi Y, Semizarov D, Wang G, McGonigal T, Roberts L, Lasko L, Palma J, et al. (2009) Acquired resistance to combination treatment with temozolomide and ABT-888 is mediated by both base excision repair and homologous recombination DNA repair pathways. Mol Cancer Res 7:1686-1692.
-
(2009)
Mol Cancer Res
, vol.7
, pp. 1686-1692
-
-
Liu, X.1
Han, E.K.2
Anderson, M.3
Shi, Y.4
Semizarov, D.5
Wang, G.6
McGonigal, T.7
Roberts, L.8
Lasko, L.9
Palma, J.10
-
58
-
-
80053446154
-
Structural studies of the PARP-1 BRCT domain
-
Loeffler PA, Cuneo MJ, Mueller GA, DeRose EF, Gabel SA, and London RE (2011) Structural studies of the PARP-1 BRCT domain. BMC Struct Biol 11:37.
-
(2011)
BMC Struct Biol
, vol.11
, pp. 37
-
-
Loeffler, P.A.1
Cuneo, M.J.2
Mueller, G.A.3
DeRose, E.F.4
Gabel, S.A.5
London, R.E.6
-
59
-
-
84856019858
-
The DNA damage response and cancer therapy
-
Lord CJ and Ashworth A (2012) The DNA damage response and cancer therapy. Nature 481:287-294.
-
(2012)
Nature
, vol.481
, pp. 287-294
-
-
Lord, C.J.1
Ashworth, A.2
-
60
-
-
84857891632
-
On PAR with PARP: Cellular stress signaling through poly(ADP-ribose) and PARP-1
-
Luo X and Kraus WL (2012) On PAR with PARP: cellular stress signaling through poly(ADP-ribose) and PARP-1. Genes Dev 26:417-432.
-
(2012)
Genes Dev
, vol.26
, pp. 417-432
-
-
Luo, X.1
Kraus, W.L.2
-
61
-
-
84905251990
-
Inhibition of poly(ADP-ribosyl)ation in cancer: Old and new paradigms revisited
-
Lupo B and Trusolino L (2014) Inhibition of poly(ADP-ribosyl)ation in cancer: old and new paradigms revisited. Biochim Biophys Acta 1846:201-215.
-
(2014)
Biochim Biophys Acta
, vol.1846
, pp. 201-215
-
-
Lupo, B.1
Trusolino, L.2
-
62
-
-
84897083413
-
Conformational activation of poly(ADP-ribose) polymerase-1 upon DNA binding revealed by small-angle X-ray scattering
-
Mansoorabadi SO, Wu M, Tao Z, Gao P, Pingali SV, Guo L, and Liu HW (2014) Conformational activation of poly(ADP-ribose) polymerase-1 upon DNA binding revealed by small-angle X-ray scattering. Biochemistry 53:1779-1788.
-
(2014)
Biochemistry
, vol.53
, pp. 1779-1788
-
-
Mansoorabadi, S.O.1
Wu, M.2
Tao, Z.3
Gao, P.4
Pingali, S.V.5
Guo, L.6
Liu, H.W.7
-
63
-
-
84905390376
-
Investigating the allosteric reverse signalling of PARP inhibitors with microsecond molecular dynamic simulations and fluorescence anisotropy
-
Marchand JR, Carotti A, Passeri D, Filipponi P, Liscio P, Camaioni E, Pellicciari R, Gioiello A, and Macchiarulo A (2014) Investigating the allosteric reverse signalling of PARP inhibitors with microsecond molecular dynamic simulations and fluorescence anisotropy. Biochim Biophys Acta 1844:1765-1772.
-
(2014)
Biochim Biophys Acta
, vol.1844
, pp. 1765-1772
-
-
Marchand, J.R.1
Carotti, A.2
Passeri, D.3
Filipponi, P.4
Liscio, P.5
Camaioni, E.6
Pellicciari, R.7
Gioiello, A.8
Macchiarulo, A.9
-
64
-
-
33748065304
-
Deficiency in the repair of DNA damage by homologous recombination and sensitivity to poly(ADP-ribose) polymerase inhibition
-
McCabe N, Turner NC, Lord CJ, Kluzek K, Bialkowska A, Swift S, Giavara S, O'Connor MJ, Tutt AN, Zdzienicka MZ, et al. (2006) Deficiency in the repair of DNA damage by homologous recombination and sensitivity to poly(ADP-ribose) polymerase inhibition. Cancer Res 66:8109-8115.
-
(2006)
Cancer Res
, vol.66
, pp. 8109-8115
-
-
McCabe, N.1
Turner, N.C.2
Lord, C.J.3
Kluzek, K.4
Bialkowska, A.5
Swift, S.6
Giavara, S.7
O'Connor, M.J.8
Tutt, A.N.9
Zdzienicka, M.Z.10
-
65
-
-
34548763143
-
Nonclassic functions of human topoisomerase I: Genome-wide and pharmacologic analyses
-
Miao ZH, Player A, Shankavaram U, Wang YH, Zimonjic DB, Lorenzi PL, Liao ZY, Liu H, Shimura T, Zhang HL, et al. (2007) Nonclassic functions of human topoisomerase I: genome-wide and pharmacologic analyses. Cancer Res 67: 8752-8761.
-
(2007)
Cancer Res
, vol.67
, pp. 8752-8761
-
-
Miao, Z.H.1
Player, A.2
Shankavaram, U.3
Wang, Y.H.4
Zimonjic, D.B.5
Lorenzi, P.L.6
Liao, Z.Y.7
Liu, H.8
Shimura, T.9
Zhang, H.L.10
-
66
-
-
84875163620
-
Cisplatin resistance associated with PARP hyperactivation
-
Michels J, Vitale I, Galluzzi L, Adam J, Olaussen KA, Kepp O, Senovilla L, Talhaoui I, Guegan J, Enot DP, et al. (2013) Cisplatin resistance associated with PARP hyperactivation. Cancer Res 73:2271-2280.
-
(2013)
Cancer Res
, vol.73
, pp. 2271-2280
-
-
Michels, J.1
Vitale, I.2
Galluzzi, L.3
Adam, J.4
Olaussen, K.A.5
Kepp, O.6
Senovilla, L.7
Talhaoui, I.8
Guegan, J.9
Enot, D.P.10
-
67
-
-
0029119615
-
Characterisation of a gain-of-function mutant of poly(ADP-ribose) polymerase
-
Miranda EA, Dantzer F, O'Farrell M, de Murcia G, and de Murcia JM (1995) Characterisation of a gain-of-function mutant of poly(ADP-ribose) polymerase. Biochem Biophys Res Commun 212:317-325.
-
(1995)
Biochem Biophys Res Commun
, vol.212
, pp. 317-325
-
-
Miranda, E.A.1
Dantzer, F.2
O'Farrell, M.3
De Murcia, G.4
De Murcia, J.M.5
-
68
-
-
67649983992
-
Synthesis and SAR of novel tricyclic quinoxalinone inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1)
-
Miyashiro J, Woods KW, Park CH, Liu X, Shi Y, Johnson EF, Bouska JJ, Olson AM, Luo Y, Fry EH, et al. (2009) Synthesis and SAR of novel tricyclic quinoxalinone inhibitors of poly(ADP-ribose)polymerase-1 (PARP-1). Bioorg Med Chem Lett 19: 4050-4054.
-
(2009)
Bioorg Med Chem Lett
, vol.19
, pp. 4050-4054
-
-
Miyashiro, J.1
Woods, K.W.2
Park, C.H.3
Liu, X.4
Shi, Y.5
Johnson, E.F.6
Bouska, J.J.7
Olson, A.M.8
Luo, Y.9
Fry, E.H.10
-
69
-
-
84868221110
-
Trapping of PARP1 and PARP2 by clinical PARP inhibitors
-
Murai J, Huang SY, Das BB, Renaud A, Zhang Y, Doroshow JH, Ji J, Takeda S, and Pommier Y (2012) Trapping of PARP1 and PARP2 by clinical PARP inhibitors. Cancer Res 72:5588-5599.
-
(2012)
Cancer Res
, vol.72
, pp. 5588-5599
-
-
Murai, J.1
Huang, S.Y.2
Das, B.B.3
Renaud, A.4
Zhang, Y.5
Doroshow, J.H.6
Ji, J.7
Takeda, S.8
Pommier, Y.9
-
70
-
-
84894121635
-
Stereospecific PARP trapping by BMN 673 and comparison with olaparib and rucaparib
-
Murai J, Huang SY, Renaud A, Zhang Y, Ji J, Takeda S, Morris J, Teicher B, Doroshow JH, and Pommier Y (2014a) Stereospecific PARP trapping by BMN 673 and comparison with olaparib and rucaparib. Mol Cancer Ther 13:433-443.
-
(2014)
Mol Cancer Ther
, vol.13
, pp. 433-443
-
-
Murai, J.1
Huang, S.Y.2
Renaud, A.3
Zhang, Y.4
Ji, J.5
Takeda, S.6
Morris, J.7
Teicher, B.8
Doroshow, J.H.9
Pommier, Y.10
-
71
-
-
84901218339
-
Rationale for poly(ADP-ribose) polymerase (PARP) inhibitors in combination therapy with camptothecins or temozolomide based on PARP trapping versus catalytic inhibition
-
Murai J, Zhang Y, Morris J, Ji J, Takeda S, Doroshow JH, and Pommier Y (2014b) Rationale for poly(ADP-ribose) polymerase (PARP) inhibitors in combination therapy with camptothecins or temozolomide based on PARP trapping versus catalytic inhibition. J Pharmacol Exp Ther 349:408-416.
-
(2014)
J Pharmacol Exp Ther
, vol.349
, pp. 408-416
-
-
Murai, J.1
Zhang, Y.2
Morris, J.3
Ji, J.4
Takeda, S.5
Doroshow, J.H.6
Pommier, Y.7
-
72
-
-
84856879500
-
Structural basis of selective inhibition of human tankyrases
-
Narwal M, Venkannagari H, and Lehtiö L (2012) Structural basis of selective inhibition of human tankyrases. J Med Chem 55:1360-1367.
-
(2012)
J Med Chem
, vol.55
, pp. 1360-1367
-
-
Narwal, M.1
Venkannagari, H.2
Lehtiö, L.3
-
73
-
-
0000536643
-
DNA topoisomerase-targeting antitumor drugs can be studied in yeast
-
Nitiss J and Wang JC (1988) DNA topoisomerase-targeting antitumor drugs can be studied in yeast. Proc Natl Acad Sci USA 85:7501-7505.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 7501-7505
-
-
Nitiss, J.1
Wang, J.C.2
-
74
-
-
84867409347
-
Synthetic lethal interactions between EGFR and PARP inhibition in human triple negative breast cancer cells
-
Nowsheen S, Cooper T, Stanley JA, and Yang ES (2012) Synthetic lethal interactions between EGFR and PARP inhibition in human triple negative breast cancer cells. PLoS One 7:e46614.
-
(2012)
PLoS One
, vol.7
-
-
Nowsheen, S.1
Cooper, T.2
Stanley, J.A.3
Yang, E.S.4
-
75
-
-
65549158566
-
Topoisomerase II alpha and responsiveness of breast cancer to adjuvant chemotherapy
-
O'Malley FP, Chia S, Tu D, Shepherd LE, Levine MN, Bramwell VH, Andrulis IL, and Pritchard KI (2009) Topoisomerase II alpha and responsiveness of breast cancer to adjuvant chemotherapy. J Natl Cancer Inst 101:644-650.
-
(2009)
J Natl Cancer Inst
, vol.101
, pp. 644-650
-
-
O'Malley, F.P.1
Chia, S.2
Tu, D.3
Shepherd, L.E.4
Levine, M.N.5
Bramwell, V.H.6
Andrulis, I.L.7
Pritchard, K.I.8
-
77
-
-
84856738573
-
Enhanced killing of cancer cells by poly(ADP-ribose) polymerase inhibitors and topoisomerase I inhibitors reflects poisoning of both enzymes
-
Patel AG, Flatten KS, Schneider PA, Dai NT, McDonald JS, Poirier GG, and Kaufmann SH (2012) Enhanced killing of cancer cells by poly(ADP-ribose) polymerase inhibitors and topoisomerase I inhibitors reflects poisoning of both enzymes. J Biol Chem 287:4198-4210.
-
(2012)
J Biol Chem
, vol.287
, pp. 4198-4210
-
-
Patel, A.G.1
Flatten, K.S.2
Schneider, P.A.3
Dai, N.T.4
McDonald, J.S.5
Poirier, G.G.6
Kaufmann, S.H.7
-
78
-
-
84904325637
-
Discovery and structure-activity relationship of novel 2,3-dihydrobenzofuran-7-carboxamide and 2,3-dihydrobenzofuran-3(2H)-one-7-carboxamide derivatives as poly(ADP-ribose)polymerase-1 inhibitors
-
Patel MR, Bhatt A, Steffen JD, Chergui A, Murai J, Pommier Y, Pascal JM, Trombetta LD, Fronczek FR, and Talele TT (2014) Discovery and structure-activity relationship of novel 2,3-dihydrobenzofuran-7-carboxamide and 2,3-dihydrobenzofuran-3(2H)-one-7-carboxamide derivatives as poly(ADP-ribose)polymerase-1 inhibitors. J Med Chem 57: 5579-5601.
-
(2014)
J Med Chem
, vol.57
, pp. 5579-5601
-
-
Patel, M.R.1
Bhatt, A.2
Steffen, J.D.3
Chergui, A.4
Murai, J.5
Pommier, Y.6
Pascal, J.M.7
Trombetta, L.D.8
Fronczek, F.R.9
Talele, T.T.10
-
79
-
-
79959265786
-
Discovery and characterization of novel potent PARP-1 inhibitors endowed with neuroprotective properties: From TIQ-A to HYDAMTIQ
-
Pellicciari R, Camaioni E, Gilbert AM, Macchiarulo A, Bikker JA, Shah F, Bard J, Constantino G, Gioiello A, Robertson GM, et al. (2011) Discovery and characterization of novel potent PARP-1 inhibitors endowed with neuroprotective properties: from TIQ-A to HYDAMTIQ. Med Chem Commun 2:559-565.
-
(2011)
Med Chem Commun
, vol.2
, pp. 559-565
-
-
Pellicciari, R.1
Camaioni, E.2
Gilbert, A.M.3
Macchiarulo, A.4
Bikker, J.A.5
Shah, F.6
Bard, J.7
Constantino, G.8
Gioiello, A.9
Robertson, G.M.10
-
80
-
-
79955454978
-
Exploiting the homologous recombination DNA repair network for targeted cancer therapy
-
Peng G and Lin SY (2011) Exploiting the homologous recombination DNA repair network for targeted cancer therapy. World J Clin Oncol 2:73-79.
-
(2011)
World J Clin Oncol
, vol.2
, pp. 73-79
-
-
Peng, G.1
Lin, S.Y.2
-
81
-
-
60549117554
-
Discovery of the poly(ADP-ribose) polymerase (PARP) inhibitor 2-[(R)-2-methylpyrrolidin-2-yl]-1H-benzimidazole-4-carboxamide (ABT-888) for the treatment of cancer
-
Penning TD, Zhu GD, Gandhi VB, Gong J, Liu X, Shi Y, Klinghofer V, Johnson EF, Donawho CK, Frost DJ, et al. (2009) Discovery of the Poly(ADP-ribose) polymerase (PARP) inhibitor 2-[(R)-2-methylpyrrolidin-2-yl]-1H-benzimidazole-4-carboxamide (ABT-888) for the treatment of cancer. J Med Chem 52:514-523.
-
(2009)
J Med Chem
, vol.52
, pp. 514-523
-
-
Penning, T.D.1
Zhu, G.D.2
Gandhi, V.B.3
Gong, J.4
Liu, X.5
Shi, Y.6
Klinghofer, V.7
Johnson, E.F.8
Donawho, C.K.9
Frost, D.J.10
-
82
-
-
77951110744
-
Optimization of phenyl-substituted benzimidazole carboxamide poly(ADP-ribose) polymerase inhibitors: Identification of (S)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-1H-benzimidazole-4-carboxamide (A-966492), a highly potent and efficacious inhibitor
-
Penning TD, Zhu GD, Gong J, Thomas S, Gandhi VB, Liu X, Shi Y, Klinghofer V, Johnson EF, Park CH, et al. (2010) Optimization of phenyl-substituted benzimidazole carboxamide poly(ADP-ribose) polymerase inhibitors: identification of (S)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-1H-benzimidazole-4-carboxamide (A-966492), a highly potent and efficacious inhibitor. J Med Chem 53:3142-3153.
-
(2010)
J Med Chem
, vol.53
, pp. 3142-3153
-
-
Penning, T.D.1
Zhu, G.D.2
Gong, J.3
Thomas, S.4
Gandhi, V.B.5
Liu, X.6
Shi, Y.7
Klinghofer, V.8
Johnson, E.F.9
Park, C.H.10
-
83
-
-
84876715061
-
A genetic screen using the PiggyBac transposon in haploid cells identifies parp1 as a mediator of olaparib toxicity
-
Pettitt SJ, Rehman FL, Bajrami I, Brough R, Wallberg F, Kozarewa I, Fenwick K, Assiotis I, Chen L, Campbell J, et al. (2013) A genetic screen using the PiggyBac transposon in haploid cells identifies Parp1 as a mediator of olaparib toxicity. PLoS One 8:e61520.
-
(2013)
PLoS One
, vol.8
-
-
Pettitt, S.J.1
Rehman, F.L.2
Bajrami, I.3
Brough, R.4
Wallberg, F.5
Kozarewa, I.6
Fenwick, K.7
Assiotis, I.8
Chen, L.9
Campbell, J.10
-
84
-
-
84871689343
-
Development and validation of an immunoassay for quantification of topoisomerase I in solid tumor tissues
-
Pfister TD, Hollingshead M, Kinders RJ, Zhang Y, Evrard YA, Ji J, Khin SA, Borgel S, Stotler H, Carter J, et al. (2012) Development and validation of an immunoassay for quantification of topoisomerase I in solid tumor tissues. PLoS One 7:e50494.
-
(2012)
PLoS One
, vol.7
-
-
Pfister, T.D.1
Hollingshead, M.2
Kinders, R.J.3
Zhang, Y.4
Evrard, Y.A.5
Ji, J.6
Khin, S.A.7
Borgel, S.8
Stotler, H.9
Carter, J.10
-
85
-
-
67651176020
-
Topoisomerase I levels in the NCI-60 cancer cell line panel determined by validated ELISA and microarray analysis and correlation with indenoisoquinoline sensitivity
-
Pfister TD, Reinhold WC, Agama K, Gupta S, Khin SA, Kinders RJ, Parchment RE, Tomaszewski JE, Doroshow JH, and Pommier Y (2009) Topoisomerase I levels in the NCI-60 cancer cell line panel determined by validated ELISA and microarray analysis and correlation with indenoisoquinoline sensitivity. Mol Cancer Ther 8: 1878-1884.
-
(2009)
Mol Cancer Ther
, vol.8
, pp. 1878-1884
-
-
Pfister, T.D.1
Reinhold, W.C.2
Agama, K.3
Gupta, S.4
Khin, S.A.5
Kinders, R.J.6
Parchment, R.E.7
Tomaszewski, J.E.8
Doroshow, J.H.9
Pommier, Y.10
-
86
-
-
84877920585
-
A phase II study of the potent PARP inhibitor, rucaparib (PF-01367338, AG014699), with temozolomide in patients with metastatic melanoma demonstrating evidence of chemopotentiation
-
Plummer R, Lorigan P, Steven N, Scott L, Middleton MR, Wilson RH, Mulligan E, Curtin N, Wang D, Dewji R, et al. (2013) A phase II study of the potent PARP inhibitor, rucaparib (PF-01367338, AG014699), with temozolomide in patients with metastatic melanoma demonstrating evidence of chemopotentiation. Cancer Chemother Pharmacol 71:1191-1199.
-
(2013)
Cancer Chemother Pharmacol
, vol.71
, pp. 1191-1199
-
-
Plummer, R.1
Lorigan, P.2
Steven, N.3
Scott, L.4
Middleton, M.R.5
Wilson, R.H.6
Mulligan, E.7
Curtin, N.8
Wang, D.9
Dewji, R.10
-
87
-
-
84872547120
-
Drugging topoisomerases: Lessons and challenges
-
Pommier Y (2013) Drugging topoisomerases: lessons and challenges. ACS Chem Biol 8:82-95.
-
(2013)
ACS Chem Biol
, vol.8
, pp. 82-95
-
-
Pommier, Y.1
-
88
-
-
33745278845
-
Repair of topoisomerase I-mediated DNA damage
-
Pommier Y, Barcelo JM, Rao VA, Sordet O, Jobson AG, Thibaut L, Miao ZH, Seiler JA, Zhang H, Marchand C, et al. (2006) Repair of topoisomerase I-mediated DNA damage. Prog Nucleic Acid Res Mol Biol 81:179-229.
-
(2006)
Prog Nucleic Acid Res Mol Biol
, vol.81
, pp. 179-229
-
-
Pommier, Y.1
Barcelo, J.M.2
Rao, V.A.3
Sordet, O.4
Jobson, A.G.5
Thibaut, L.6
Miao, Z.H.7
Seiler, J.A.8
Zhang, H.9
Marchand, C.10
-
89
-
-
77954187741
-
DNA topoisomerases and their poisoning by anticancer and antibacterial drugs
-
Pommier Y, Leo E, Zhang H, and Marchand C (2010) DNA topoisomerases and their poisoning by anticancer and antibacterial drugs. Chem Biol 17:421-433.
-
(2010)
Chem Biol
, vol.17
, pp. 421-433
-
-
Pommier, Y.1
Leo, E.2
Zhang, H.3
Marchand, C.4
-
90
-
-
84855347756
-
Interfacial inhibitors: Targeting macromolecular complexes
-
Pommier Y and Marchand C (2011) Interfacial inhibitors: targeting macromolecular complexes. Nat Rev Drug Discov 11:25-36.
-
(2011)
Nat Rev Drug Discov
, vol.11
, pp. 25-36
-
-
Pommier, Y.1
Marchand, C.2
-
91
-
-
0033208192
-
Topoisomerase I inhibitors: Selectivity and cellular resistance
-
Pommier Y, Pourquier P, Urasaki Y, Wu J, and Laco GS (1999) Topoisomerase I inhibitors: selectivity and cellular resistance. Drug Resist Updat 2:307-318.
-
(1999)
Drug Resist Updat
, vol.2
, pp. 307-318
-
-
Pommier, Y.1
Pourquier, P.2
Urasaki, Y.3
Wu, J.4
Laco, G.S.5
-
92
-
-
0344394180
-
Mechanisms of resistance to topoisomerase I-targeting drugs
-
Rasheed ZA and Rubin EH (2003) Mechanisms of resistance to topoisomerase I-targeting drugs. Oncogene 22:7296-7304.
-
(2003)
Oncogene
, vol.22
, pp. 7296-7304
-
-
Rasheed, Z.A.1
Rubin, E.H.2
-
93
-
-
0032489634
-
Crystal structures of human topoisomerase I in covalent and noncovalent complexes with DNA
-
Redinbo MR, Stewart L, Kuhn P, Champoux JJ, and Hol WG (1998) Crystal structures of human topoisomerase I in covalent and noncovalent complexes with DNA. Science 279:1504-1513.
-
(1998)
Science
, vol.279
, pp. 1504-1513
-
-
Redinbo, M.R.1
Stewart, L.2
Kuhn, P.3
Champoux, J.J.4
Hol, W.G.5
-
94
-
-
84941590234
-
Developing rational drug combination strategies for PARP inhibitors
-
3050
-
Rehman F, Elliott R, Brough R, Frankum J, Ragab A, Lord CJ, and Ashworth A (2012) Developing rational drug combination strategies for PARP inhibitors. J Clin Oncol 30 (suppl; abstr 3050).
-
(2012)
J Clin Oncol
, vol.30
-
-
Rehman, F.1
Elliott, R.2
Brough, R.3
Frankum, J.4
Ragab, A.5
Lord, C.J.6
Ashworth, A.7
-
95
-
-
77950023283
-
PARP inhibition: Parp1 and beyond
-
Rouleau M, Patel A, Hendzel MJ, Kaufmann SH, and Poirier GG (2010) PARP inhibition: PARP1 and beyond. Nat Rev Cancer 10:293-301.
-
(2010)
Nat Rev Cancer
, vol.10
, pp. 293-301
-
-
Rouleau, M.1
Patel, A.2
Hendzel, M.J.3
Kaufmann, S.H.4
Poirier, G.G.5
-
96
-
-
0032562650
-
The mechanism of the elongation and branching reaction of poly(ADP-ribose) polymerase as derived from crystal structures and mutagenesis
-
Ruf A, Rolli V, de Murcia G, and Schulz GE (1998) The mechanism of the elongation and branching reaction of poly(ADP-ribose) polymerase as derived from crystal structures and mutagenesis. J Mol Biol 278:57-65.
-
(1998)
J Mol Biol
, vol.278
, pp. 57-65
-
-
Ruf, A.1
Rolli, V.2
De Murcia, G.3
Schulz, G.E.4
-
97
-
-
49649104978
-
Mechanisms of chemoresistance to alkylating agents in malignant glioma
-
Sarkaria JN, Kitange GJ, James CD, Plummer R, Calvert H, Weller M, and Wick W (2008) Mechanisms of chemoresistance to alkylating agents in malignant glioma. Clin Cancer Res 14:2900-2908.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 2900-2908
-
-
Sarkaria, J.N.1
Kitange, G.J.2
James, C.D.3
Plummer, R.4
Calvert, H.5
Weller, M.6
Wick, W.7
-
98
-
-
0026507413
-
Role of poly(ADP-ribose) formation in DNA repair
-
Satoh MS and Lindahl T (1992) Role of poly(ADP-ribose) formation in DNA repair. Nature 356:356-358.
-
(1992)
Nature
, vol.356
, pp. 356-358
-
-
Satoh, M.S.1
Lindahl, T.2
-
100
-
-
84884576079
-
BMN 673, a novel and highly potent PARP1/2 inhibitor for the treatment of human cancers with DNA repair deficiency
-
Shen Y, Rehman FL, Feng Y, Boshuizen J, Bajrami I, Elliott R, Wang B, Lord CJ, Post LE, and Ashworth A (2013) BMN 673, a novel and highly potent PARP1/2 inhibitor for the treatment of human cancers with DNA repair deficiency. Clin Cancer Res 19:5003-5015.
-
(2013)
Clin Cancer Res
, vol.19
, pp. 5003-5015
-
-
Shen, Y.1
Rehman, F.L.2
Feng, Y.3
Boshuizen, J.4
Bajrami, I.5
Elliott, R.6
Wang, B.7
Lord, C.J.8
Post, L.E.9
Ashworth, A.10
-
101
-
-
84941590235
-
Mechanisms of resistance to the PARP inhibitor BMN 673 in ewing's sarcoma
-
2013 30 Oct-2 Nov; New York, NY
-
Singh A, Bartosz C, Jia W, Clark K, Dering J, Anderson L, Federman N, Eilber FC, Shen Y, Finn R, et al. (2013) Mechanisms of resistance to the PARP inhibitor BMN 673 in Ewing's sarcoma. Connective Tissue Oncology Society 18th Annual Meeting; 2013 30 Oct-2 Nov; New York, NY.
-
(2013)
Connective Tissue Oncology Society 18th Annual Meeting
-
-
Singh, A.1
Bartosz, C.2
Jia, W.3
Clark, K.4
Dering, J.5
Anderson, L.6
Federman, N.7
Eilber, F.C.8
Shen, Y.9
Finn, R.10
-
102
-
-
84923164096
-
Synergistic activity of PARP inhibition by talazoparib (BMN 673) with temozolomide in pediatric cancer models in the pediatric preclinical testing program
-
Smith MA, Reynolds CP, Kang MH, Kolb EA, Gorlick R, Carol H, Lock RB, Keir ST, Maris JM, Billups CA, et al. (2015) Synergistic activity of PARP inhibition by talazoparib (BMN 673) with temozolomide in pediatric cancer models in the pediatric preclinical testing program. Clin Cancer Res 21:819-832.
-
(2015)
Clin Cancer Res
, vol.21
, pp. 819-832
-
-
Smith, M.A.1
Reynolds, C.P.2
Kang, M.H.3
Kolb, E.A.4
Gorlick, R.5
Carol, H.6
Lock, R.B.7
Keir, S.T.8
Maris, J.M.9
Billups, C.A.10
-
103
-
-
84941590236
-
Veliparib (ABT-888) potentiates the cytotoxic activity of DNA alkylating agents by trapping PARP onto damaged chromatin
-
2014 5-9 Apr; San Diego, CA
-
Solomon L, Hopkins T, Shi Y, Ellis P, Donawho C, Johnson EF, Fang G, and Maag D (2014) Veliparib (ABT-888) potentiates the cytotoxic activity of DNA alkylating agents by trapping PARP onto damaged chromatin. Annual Meeting of the American Association for Cancer Research; 2014 5-9 Apr; San Diego, CA.
-
(2014)
Annual Meeting of the American Association for Cancer Research
-
-
Solomon, L.1
Hopkins, T.2
Shi, Y.3
Ellis, P.4
Donawho, C.5
Johnson, E.F.6
Fang, G.7
Maag, D.8
-
105
-
-
84892696097
-
Targeting PARP-1 allosteric regulation offers therapeutic potential against cancer
-
Steffen JD, Tholey RM, Langelier MF, Planck JL, Schiewer MJ, Lal S, Bildzukewicz NA, Yeo CJ, Knudsen KE, Brody JR, et al. (2014) Targeting PARP-1 allosteric regulation offers therapeutic potential against cancer. Cancer Res 74:31-37.
-
(2014)
Cancer Res
, vol.74
, pp. 31-37
-
-
Steffen, J.D.1
Tholey, R.M.2
Langelier, M.F.3
Planck, J.L.4
Schiewer, M.J.5
Lal, S.6
Bildzukewicz, N.A.7
Yeo, C.J.8
Knudsen, K.E.9
Brody, J.R.10
-
106
-
-
84919705139
-
Targeting the DNA repair pathway in ewing sarcoma
-
Stewart E, Goshorn R, Bradley C, Griffiths LM, Benavente C, Twarog NR, Miller GM, Caufield W, Freeman BB, 3rd, Bahrami A, et al. (2014) Targeting the DNA repair pathway in Ewing sarcoma. Cell Rep 9:829-841.
-
(2014)
Cell Rep
, vol.9
, pp. 829-841
-
-
Stewart, E.1
Goshorn, R.2
Bradley, C.3
Griffiths, L.M.4
Benavente, C.5
Twarog, N.R.6
Miller, G.M.7
Caufield, W.8
Freeman, B.B.9
Bahrami, A.10
-
107
-
-
79955588797
-
Poly (ADP-ribose) polymerase (PARP) is not involved in base excision repair but PARP inhibition traps a single-strand intermediate
-
Ström CE, Johansson F, Uhlén M, Szigyarto CA, Erixon K, and Helleday T (2011) Poly (ADP-ribose) polymerase (PARP) is not involved in base excision repair but PARP inhibition traps a single-strand intermediate. Nucleic Acids Res 39:3166-3175.
-
(2011)
Nucleic Acids Res
, vol.39
, pp. 3166-3175
-
-
Ström, C.E.1
Johansson, F.2
Uhlén, M.3
Szigyarto, C.A.4
Erixon, K.5
Helleday, T.6
-
108
-
-
84860228503
-
Enhancing CHK1 inhibitor lethality in glioblastoma
-
Tang Y, Dai Y, Grant S, and Dent P (2012) Enhancing CHK1 inhibitor lethality in glioblastoma. Cancer Biol Ther 13:379-388.
-
(2012)
Cancer Biol Ther
, vol.13
, pp. 379-388
-
-
Tang, Y.1
Dai, Y.2
Grant, S.3
Dent, P.4
-
109
-
-
79954900147
-
Biomarkers of PARP inhibitor sensitivity
-
Turner NC and Ashworth A (2011) Biomarkers of PARP inhibitor sensitivity. Breast Cancer Res Treat 127:283-286.
-
(2011)
Breast Cancer Res Treat
, vol.127
, pp. 283-286
-
-
Turner, N.C.1
Ashworth, A.2
-
110
-
-
84941569601
-
Combination of a novel PARP inhibitor, BMC 673, with temozolomide for the treatment of melanoma (Abstract)
-
von Euw EM, Gong KW, Rong HM, O'Brien N, Signh A, Shen Y, Post L, Finn RS, Chmielowski B, and Slamon DJ (2014) Combination of a novel PARP inhibitor, BMC 673, with temozolomide for the treatment of melanoma (Abstract). Pigment Cell Melanoma Res 26:1011.
-
(2014)
Pigment Cell Melanoma Res
, vol.26
, pp. 1011
-
-
Von Euw, E.M.1
Gong, K.W.2
Rong, H.M.3
O'Brien, N.4
Signh, A.5
Shen, Y.6
Post, L.7
Finn, R.S.8
Chmielowski, B.9
Slamon, D.J.10
-
111
-
-
84857939963
-
Family-wide chemical profiling and structural analysis of PARP and tankyrase inhibitors
-
Wahlberg E, Karlberg T, Kouznetsova E, Markova N, Macchiarulo A, Thorsell AG, Pol E, Frostell Å, Ekblad T, Öncü D, et al. (2012) Family-wide chemical profiling and structural analysis of PARP and tankyrase inhibitors. Nat Biotechnol 30:283-288.
-
(2012)
Nat Biotechnol
, vol.30
, pp. 283-288
-
-
Wahlberg, E.1
Karlberg, T.2
Kouznetsova, E.3
Markova, N.4
Macchiarulo, A.5
Thorsell, A.G.6
Pol, E.7
Frostell, A.8
Ekblad, T.9
Öncü, D.10
-
112
-
-
84869097457
-
The structure of DNA-bound human topoisomerase II alpha: Conformational mechanisms for coordinating inter-subunit interactions with DNA cleavage
-
Wendorff TJ, Schmidt BH, Heslop P, Austin CA, and Berger JM (2012) The structure of DNA-bound human topoisomerase II alpha: conformational mechanisms for coordinating inter-subunit interactions with DNA cleavage. J Mol Biol 424:109-124.
-
(2012)
J Mol Biol
, vol.424
, pp. 109-124
-
-
Wendorff, T.J.1
Schmidt, B.H.2
Heslop, P.3
Austin, C.A.4
Berger, J.M.5
-
113
-
-
84941555603
-
Interactions between ataxia telangiectasia mutated kinase inhibition, poly(ADP-ribose) polymerase-1 inhibition and BRCA1 status in breast cancer cells
-
Węsierska-Gądek J and Heinzl S (2014) Interactions between ataxia telangiectasia mutated kinase inhibition, poly(ADP-ribose) polymerase-1 inhibition and BRCA1 status in breast cancer cells. J Cancer Prev 19:125-136.
-
(2014)
J Cancer Prev
, vol.19
, pp. 125-136
-
-
Węsierska-Gądek, J.1
Heinzl, S.2
-
114
-
-
0027276027
-
Metformin-associated lactic acidosis in Sweden 1977-1991
-
Wiholm BE and Myrhed M (1993) Metformin-associated lactic acidosis in Sweden 1977-1991. Eur J Clin Pharmacol 44:589-591.
-
(1993)
Eur J Clin Pharmacol
, vol.44
, pp. 589-591
-
-
Wiholm, B.E.1
Myrhed, M.2
-
115
-
-
84876257495
-
Design, synthesis, and biological evaluation of a series of benzo[de] [1,7]naphthyridin-7(8H)-ones bearing a functionalized longer chain appendage as novel PARP1 inhibitors
-
Ye N, Chen CH, Chen T, Song Z, He JX, Huan XJ, Song SS, Liu Q, Chen Y, Ding J, et al. (2013) Design, synthesis, and biological evaluation of a series of benzo[de] [1,7]naphthyridin-7(8H)-ones bearing a functionalized longer chain appendage as novel PARP1 inhibitors. J Med Chem 56:2885-2903.
-
(2013)
J Med Chem
, vol.56
, pp. 2885-2903
-
-
Ye, N.1
Chen, C.H.2
Chen, T.3
Song, Z.4
He, J.X.5
Huan, X.J.6
Song, S.S.7
Liu, Q.8
Chen, Y.9
Ding, J.10
-
116
-
-
79957575681
-
PARP-1 and PARP-2: New players in tumour development
-
Yelamos J, Farres J, Llacuna L, Ampurdanes C, and Martin-Caballero J (2011) PARP-1 and PARP-2: new players in tumour development. Am J Cancer Res 1: 328-346.
-
(2011)
Am J Cancer Res
, vol.1
, pp. 328-346
-
-
Yelamos, J.1
Farres, J.2
Llacuna, L.3
Ampurdanes, C.4
Martin-Caballero, J.5
-
117
-
-
84862925785
-
Temozolomide: Mechanisms of action, repair and resistance
-
Zhang J, Stevens MF, and Bradshaw TD (2012) Temozolomide: mechanisms of action, repair and resistance. Curr Mol Pharmacol 5:102-114.
-
(2012)
Curr Mol Pharmacol
, vol.5
, pp. 102-114
-
-
Zhang, J.1
Stevens, M.F.2
Bradshaw, T.D.3
-
118
-
-
79956053314
-
Poly(ADP-ribose) polymerase and XPF-ERCC1 participate in distinct pathways for the repair of topoisomerase I-induced DNA damage in mammalian cells
-
Zhang YW, Regairaz M, Seiler JA, Agama KK, Doroshow JH, and Pommier Y (2011) Poly(ADP-ribose) polymerase and XPF-ERCC1 participate in distinct pathways for the repair of topoisomerase I-induced DNA damage in mammalian cells. Nucleic Acids Res 39:3607-3620.
-
(2011)
Nucleic Acids Res
, vol.39
, pp. 3607-3620
-
-
Zhang, Y.W.1
Regairaz, M.2
Seiler, J.A.3
Agama, K.K.4
Doroshow, J.H.5
Pommier, Y.6
|