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Volumn 31, Issue 2, 2013, Pages 461-468

The PARP inhibitor ABT-888 synergizes irinotecan treatment of colon cancer cell lines

Author keywords

Colon cancer; Irinotecan; PARP; PARP inhibitor; SN38; VE 821

Indexed keywords

FIRTECAN; HISTONE H2AX; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE 1; OXALIPLATIN; VELIPARIB;

EID: 84879555636     PISSN: 01676997     EISSN: 15730646     Source Type: Journal    
DOI: 10.1007/s10637-012-9886-7     Document Type: Article
Times cited : (55)

References (48)
  • 1
    • 77953645531 scopus 로고    scopus 로고
    • Optimal delivery of cytotoxic chemotherapy for colon cancer
    • 20526099 10.1097/PPO.0b013e3181ddc5ac 1:CAS:528:DC%2BC3cXovV2rt7g%3D
    • Raftery L, Goldberg RM (2010) Optimal delivery of cytotoxic chemotherapy for colon cancer. Cancer J 16:214-219
    • (2010) Cancer J , vol.16 , pp. 214-219
    • Raftery, L.1    Goldberg, R.M.2
  • 2
    • 39849097680 scopus 로고    scopus 로고
    • Resistance to therapy caused by intragenic deletion in BRCA2
    • 18264088 10.1038/nature06548 1:CAS:528:DC%2BD1cXisFWjtrw%3D
    • Edwards SL (2008) Resistance to therapy caused by intragenic deletion in BRCA2. Nature 451:1111-1115
    • (2008) Nature , vol.451 , pp. 1111-1115
    • Edwards, S.L.1
  • 3
    • 0036176510 scopus 로고    scopus 로고
    • Mechanisms of cancer drug resistance
    • 11818492 10.1146/annurev.med.53.082901.103929 1:CAS:528: DC%2BD38Xitl2mtLo%3D
    • Gottesman MM (2002) Mechanisms of cancer drug resistance. Annu Rev Med 53:615-627
    • (2002) Annu Rev Med , vol.53 , pp. 615-627
    • Gottesman, M.M.1
  • 4
    • 33846404174 scopus 로고    scopus 로고
    • Molecular mechanisms of resistance and toxicity associated with platinating agents
    • 17084534 10.1016/j.ctrv.2006.09.006 1:CAS:528:DC%2BD2sXhtVartrw%3D
    • Rabik CA, Dolan ME (2007) Molecular mechanisms of resistance and toxicity associated with platinating agents. Cancer Treat Rev 33:9-23
    • (2007) Cancer Treat Rev , vol.33 , pp. 9-23
    • Rabik, C.A.1    Dolan, M.E.2
  • 5
    • 0036660428 scopus 로고    scopus 로고
    • Repair of DNA interstrand crosslinks as a mechanism of clinical resistance to melphalan in multiple myeloma
    • 12070031 10.1182/blood.V100.1.224 1:CAS:528:DC%2BD38XltF2rsbY%3D
    • Spanswick VJ, Craddock C, Sekhar M, Mahendra P, Shankaranarayana P, Hughes RG (2002) Repair of DNA interstrand crosslinks as a mechanism of clinical resistance to melphalan in multiple myeloma. Blood 100:224-229
    • (2002) Blood , vol.100 , pp. 224-229
    • Spanswick, V.J.1    Craddock, C.2    Sekhar, M.3    Mahendra, P.4    Shankaranarayana, P.5    Hughes, R.G.6
  • 6
    • 34248594725 scopus 로고    scopus 로고
    • Chlorambucil cytotoxicity in malignant B lymphocytes is synergistically increased by 2-(morpholin-4-yl)-benzo[h]chomen-4-one (NU7026)-mediated inhibition of DNA double-strand break repair via inhibition of DNA-dependent protein kinase
    • 17351105 10.1124/jpet.106.118356 1:CAS:528:DC%2BD2sXmsFeru74%3D
    • Amrein L, Loignon M, Goulet A-C, Dunn M, Jean-Claude B, Aloyz R, et al. (2007) Chlorambucil cytotoxicity in malignant B lymphocytes is synergistically increased by 2-(morpholin-4-yl)-benzo[h]chomen-4-one (NU7026)-mediated inhibition of DNA double-strand break repair via inhibition of DNA-dependent protein kinase. J Pharmacol Exp Ther 321:848-855
    • (2007) J Pharmacol Exp Ther , vol.321 , pp. 848-855
    • Amrein, L.1    Loignon, M.2    Goulet, A.-C.3    Dunn, M.4    Jean-Claude, B.5    Aloyz, R.6
  • 7
    • 84864328191 scopus 로고    scopus 로고
    • Irinotecan and DNA-PKcs inhibitors synergize in killing of colon cancer cells
    • 21221710 10.1007/s10637-010-9626-9 1:CAS:528:DC%2BC38XmvFamsLo%3D
    • Davidson D, Coulombe Y, Martinez-Marignac V, Amrein L, Grenier J, Hodkinson K, et al. (2012) Irinotecan and DNA-PKcs inhibitors synergize in killing of colon cancer cells. Invest New Drugs 30:1248-1256
    • (2012) Invest New Drugs , vol.30 , pp. 1248-1256
    • Davidson, D.1    Coulombe, Y.2    Martinez-Marignac, V.3    Amrein, L.4    Grenier, J.5    Hodkinson, K.6
  • 8
    • 84866736846 scopus 로고    scopus 로고
    • Effects of the novel DNA dependent protein kinase inhibitor, IC486241, on the DNA damage response to doxorubicin and cisplatin in breast cancer cells
    • 21567185 10.1007/s10637-011-9678-5 1:CAS:528:DC%2BC38XpvVylu7s%3D
    • Davidson D, Grenier J, Martinez-Marignac V, Amrein L, Shawi M, Tokars M, et al. (2012) Effects of the novel DNA dependent protein kinase inhibitor, IC486241, on the DNA damage response to doxorubicin and cisplatin in breast cancer cells. Invest New Drugs 30:1736-1742
    • (2012) Invest New Drugs , vol.30 , pp. 1736-1742
    • Davidson, D.1    Grenier, J.2    Martinez-Marignac, V.3    Amrein, L.4    Shawi, M.5    Tokars, M.6
  • 9
    • 27644509749 scopus 로고    scopus 로고
    • Preclinical pharmacokinetics and metabolism of a novel prototype DNA-PK inhibitor NU7026
    • 16249792 1:CAS:528:DC%2BD2MXhtFChsL3E
    • Nutley BP, Smith NF, Hayes A, Kelland LR, Brunton L, Golding BT, et al. (2005) Preclinical pharmacokinetics and metabolism of a novel prototype DNA-PK inhibitor NU7026. Br J Cancer 93:1011-1018
    • (2005) Br J Cancer , vol.93 , pp. 1011-1018
    • Nutley, B.P.1    Smith, N.F.2    Hayes, A.3    Kelland, L.R.4    Brunton, L.5    Golding, B.T.6
  • 10
    • 34249006299 scopus 로고    scopus 로고
    • ABT-888, an Orally Active Poly(ADP-Ribose) Polymerase Inhibitor that Potentiates DNA-Damaging Agents in Preclinical Tumor Models
    • 17473206 10.1158/1078-0432.CCR-06-3039 1:CAS:528:DC%2BD2sXkslOhurg%3D
    • Donawho CK, Luo Y, Luo Y, Penning TD, Bauch JL, Bouska JJ, et al. (2007) ABT-888, an Orally Active Poly(ADP-Ribose) Polymerase Inhibitor that Potentiates DNA-Damaging Agents in Preclinical Tumor Models. Clin Cancer Res 13:2728-2737
    • (2007) Clin Cancer Res , vol.13 , pp. 2728-2737
    • Donawho, C.K.1    Luo, Y.2    Luo, Y.3    Penning, T.D.4    Bauch, J.L.5    Bouska, J.J.6
  • 11
    • 68849128273 scopus 로고    scopus 로고
    • Poly(ADP-ribose) polymerase inhibitor ABT-888 potentiates the cytotoxic activity of temozolomide in leukemia cells: Influence of mismatch repair status and O6-methylguanine-DNA methyltransferase activity
    • 19671751 10.1158/1535-7163.MCT-09-0142 1:CAS:528:DC%2BD1MXpvFCnu7k%3D
    • Horton TM, Jenkins G, Pati D, Zhang L, Dolan ME, Ribes-Zamora A, et al. (2009) Poly(ADP-ribose) polymerase inhibitor ABT-888 potentiates the cytotoxic activity of temozolomide in leukemia cells: influence of mismatch repair status and O6-methylguanine-DNA methyltransferase activity. Mol Cancer Ther 8:2232-2242
    • (2009) Mol Cancer Ther , vol.8 , pp. 2232-2242
    • Horton, T.M.1    Jenkins, G.2    Pati, D.3    Zhang, L.4    Dolan, M.E.5    Ribes-Zamora, A.6
  • 12
    • 84857092267 scopus 로고    scopus 로고
    • Pharmacodynamic and pathway analysis of three presumed inhibitors of poly (ADP-ribose) polymerase: ABT-888, AZD2281, and BSI201
    • 2011 April 2-6; Orlando, FL. Philidelphia, PA: American Association of Cancer Research
    • Ji J, Lee M, Kadota M, Zhang Y, Parchment R, Tomaszewski JE, et al. (2011) Pharmacodynamic and pathway analysis of three presumed inhibitors of poly (ADP-ribose) polymerase: ABT-888, AZD2281, and BSI201. Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research; 2011 April 2-6; Orlando, FL. Philidelphia, PA: American Association of Cancer Research
    • (2011) Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research
    • Ji, J.1    Lee, M.2    Kadota, M.3    Zhang, Y.4    Parchment, R.5    Tomaszewski, J.E.6
  • 13
    • 66849106010 scopus 로고    scopus 로고
    • Phase 0 clinical trial of the poly (ADP-ribose) polymerase inhibitor ABT-888 in patients with advanced malignancies
    • 19364967 10.1200/JCO.2008.19.7681 1:CAS:528:DC%2BD1MXnslWitLs%3D
    • Kummar S, Kinders R, Gutierrez ME, Rubinstein L, Parchment RE, Phillips LR, et al. (2009) Phase 0 clinical trial of the poly (ADP-ribose) polymerase inhibitor ABT-888 in patients with advanced malignancies. J Clin Oncol 27:2705-2711
    • (2009) J Clin Oncol , vol.27 , pp. 2705-2711
    • Kummar, S.1    Kinders, R.2    Gutierrez, M.E.3    Rubinstein, L.4    Parchment, R.E.5    Phillips, L.R.6
  • 14
    • 31044446360 scopus 로고    scopus 로고
    • PARP inhibitors for cancer therapy
    • 15836799 10.1017/S146239940500904X
    • Curtin NJ (2005) PARP inhibitors for cancer therapy. Expert Rev Mol Med 7:1-20
    • (2005) Expert Rev Mol Med , vol.7 , pp. 1-20
    • Curtin, N.J.1
  • 15
    • 77955272550 scopus 로고    scopus 로고
    • Alkylation DNA damage in combination with PARP inhibition results in formation of S-phase-dependent double-strand breaks
    • 20573551 10.1016/j.dnarep.2010.05.007 1:CAS:528:DC%2BC3cXpsFeqsrY%3D
    • Heacock ML, Stefanick DF, Horton JK, Wilson SH (2010) Alkylation DNA damage in combination with PARP inhibition results in formation of S-phase-dependent double-strand breaks. DNA Repair 9:929-936
    • (2010) DNA Repair , vol.9 , pp. 929-936
    • Heacock, M.L.1    Stefanick, D.F.2    Horton, J.K.3    Wilson, S.H.4
  • 16
    • 80052168685 scopus 로고    scopus 로고
    • The underlying mechanism for the PARP and BRCA synthetic lethality: Clearing up the misunderstandings
    • Helleday T. The underlying mechanism for the PARP and BRCA synthetic lethality: Clearing up the misunderstandings. Molecular Oncology; 5:387-393.
    • Molecular Oncology , vol.5 , pp. 387-393
    • Helleday, T.1
  • 17
    • 80053966336 scopus 로고    scopus 로고
    • The role of PARP in DNA repair and its therapeutic exploitation
    • 21989215 10.1038/bjc.2011.382 1:CAS:528:DC%2BC3MXhtlahsr3I
    • Javle M, Curtin NJ (2011) The role of PARP in DNA repair and its therapeutic exploitation. Br J Cancer 105:1114-1122
    • (2011) Br J Cancer , vol.105 , pp. 1114-1122
    • Javle, M.1    Curtin, N.J.2
  • 18
    • 84857936584 scopus 로고    scopus 로고
    • Advances in using PARP inhibitors to treat cancer
    • 22401667 10.1186/1741-7015-10-25 1:CAS:528:DC%2BC38XmslansLY%3D
    • Kummar S, Chen A, Parchment R, Kinders R, Ji J, Tomaszewski J, et al. (2012) Advances in using PARP inhibitors to treat cancer. BMC Med 10:25
    • (2012) BMC Med , vol.10 , pp. 25
    • Kummar, S.1    Chen, A.2    Parchment, R.3    Kinders, R.4    Ji, J.5    Tomaszewski, J.6
  • 21
    • 19444375973 scopus 로고    scopus 로고
    • Chemopotentiation by PARP inhibitors in cancer therapy
    • 15911331 10.1016/j.phrs.2005.02.010 1:CAS:528:DC%2BD2MXks1Wltr8%3D
    • Tentori L, Graziani G (2005) Chemopotentiation by PARP inhibitors in cancer therapy. Pharmacol Res 52:25-33
    • (2005) Pharmacol Res , vol.52 , pp. 25-33
    • Tentori, L.1    Graziani, G.2
  • 22
    • 79957726564 scopus 로고    scopus 로고
    • Poly(ADP-ribose) polymerase-1 (PARP-1) pharmacogenetics, activity and expression analysis in cancer patients and healthy volunteers
    • 21434873 10.1042/BJ20101723 1:CAS:528:DC%2BC3MXntV2gsLg%3D
    • Zaremba T, Thomas HD, Cole M, Coulthard SA, Plummer ER, Curtin NJ (2011) Poly(ADP-ribose) polymerase-1 (PARP-1) pharmacogenetics, activity and expression analysis in cancer patients and healthy volunteers. Biochem J 436:671-679
    • (2011) Biochem J , vol.436 , pp. 671-679
    • Zaremba, T.1    Thomas, H.D.2    Cole, M.3    Coulthard, S.A.4    Plummer, E.R.5    Curtin, N.J.6
  • 23
    • 68849090462 scopus 로고    scopus 로고
    • A phase IB trial of intravenous INO-1001 plus oral temozolomide in subjects with unresectable stage-III or IV melanoma
    • 19440934 10.1080/07357900802709159 1:CAS:528:DC%2BD1MXpt1Kitbc%3D
    • Bedikian AY, Papadopoulos NE, Kim KB, Hwu WJ, Homsi J, Glass MR, et al. (2009) A phase IB trial of intravenous INO-1001 plus oral temozolomide in subjects with unresectable stage-III or IV melanoma. Cancer Invest 27:756-763
    • (2009) Cancer Invest , vol.27 , pp. 756-763
    • Bedikian, A.Y.1    Papadopoulos, N.E.2    Kim, K.B.3    Hwu, W.J.4    Homsi, J.5    Glass, M.R.6
  • 24
    • 59449085305 scopus 로고    scopus 로고
    • Phase i study of the poly(ADP-ribose) polymerase inhibitor, AG014699, in combination with temozolomide in patients with advanced solid tumors
    • 19047122 10.1158/1078-0432.CCR-08-1223 1:CAS:528:DC%2BD1cXhsVegt7%2FM
    • Plummer R, Jones C, Middleton M, Wilson R, Evans J, Olsen A, et al. (2008) Phase I study of the poly(ADP-ribose) polymerase inhibitor, AG014699, in combination with temozolomide in patients with advanced solid tumors. Clin Cancer Res 14:7917-7923
    • (2008) Clin Cancer Res , vol.14 , pp. 7917-7923
    • Plummer, R.1    Jones, C.2    Middleton, M.3    Wilson, R.4    Evans, J.5    Olsen, A.6
  • 25
    • 34347230544 scopus 로고    scopus 로고
    • Sulforhodamine B colorimetric assay for cytotoxicity screening
    • 17406391 10.1038/nprot.2006.179 1:CAS:528:DC%2BD28XhtFOitL3O
    • Vichai V, Kirtikara K (2006) Sulforhodamine B colorimetric assay for cytotoxicity screening. Nat Protoc 1:1112-1116
    • (2006) Nat Protoc , vol.1 , pp. 1112-1116
    • Vichai, V.1    Kirtikara, K.2
  • 26
    • 0027120791 scopus 로고
    • Letter Correspondence re: "greco, et al., Applications of a New Approach for the Quantitation of Drug Synergism to the Combination of c/s-Diamminedichloroplatinum and 1-tf-D-Arabinofuranosylcytosine. Cancer Res 50: 5318-5327, 1990.
    • 1643648 1:CAS:528:DyaK38Xls1ehu78%3D
    • Berenbaum M (1992) Letter Correspondence re: "Greco, et al., Applications of a New Approach for the Quantitation of Drug Synergism to the Combination of c/s-Diamminedichloroplatinum and 1-tf-D-Arabinofuranosylcytosine. Cancer Res 50: 5318-5327, 1990.". Cancer Res 52:4558-4565
    • (1992) Cancer Res , vol.52 , pp. 4558-4565
    • Berenbaum, M.1
  • 27
    • 22944467861 scopus 로고    scopus 로고
    • Xrcc3 Induces cisplatin resistance by stimulation of Rad51-related recombinational repair, S-phase checkpoint activation, and reduced apoptosis
    • 15843498 10.1124/jpet.105.084053 1:CAS:528:DC%2BD2MXntVSju70%3D
    • Xu Z-Y, Loignon M, Han F-Y, Panasci L, Aloyz R (2005) Xrcc3 Induces cisplatin resistance by stimulation of Rad51-related recombinational repair, S-phase checkpoint activation, and reduced apoptosis. J Pharmacol Exp Ther 314:495-505
    • (2005) J Pharmacol Exp Ther , vol.314 , pp. 495-505
    • Xu, Z.-Y.1    Loignon, M.2    Han, F.-Y.3    Panasci, L.4    Aloyz, R.5
  • 28
    • 33845672155 scopus 로고    scopus 로고
    • Inhibition of poly(ADP-ribose) polymerase prevents irinotecan-induced intestinal damage and enhances irinotecan/temozolomide efficacy against colon carcinoma
    • 16809434 10.1096/fj.06-5916fje 1:CAS:528:DC%2BD28Xot1GitLw%3D
    • Tentori L, Leonetti C, Scarsella M, Muzi A, Mazzon E, Vergati M, et al. (2006) Inhibition of poly(ADP-ribose) polymerase prevents irinotecan-induced intestinal damage and enhances irinotecan/temozolomide efficacy against colon carcinoma. FASEB J 20:1709-1711
    • (2006) FASEB J , vol.20 , pp. 1709-1711
    • Tentori, L.1    Leonetti, C.2    Scarsella, M.3    Muzi, A.4    Mazzon, E.5    Vergati, M.6
  • 29
    • 77958498222 scopus 로고    scopus 로고
    • The ATM-Chk2 and ATR-Chk1 Pathways in DNA Damage Signaling and Cancer
    • George FVW, George K, editors
    • Smith J, Mun Tho L, Xu N, A. Gillespie D. The ATM-Chk2 and ATR-Chk1 Pathways in DNA Damage Signaling and Cancer. In: George FVW, George K, editors. Advances in Cancer Research: Academic Press; 2010. p. 73-112.
    • (2010) Advances in Cancer Research: Academic Press , pp. 73-112
    • Smith, J.1    Mun Tho, L.2    Xu, N.3    Gillespie, D.A.4
  • 30
    • 79959397953 scopus 로고    scopus 로고
    • Synthetic lethality: Exploiting the addiction of cancer to DNA repair
    • 21441464 10.1182/blood-2011-01-313734 1:CAS:528:DC%2BC3MXotVyiu74%3D
    • Shaheen M, Allen C, Nickoloff JA, Hromas R (2011) Synthetic lethality: exploiting the addiction of cancer to DNA repair. Blood 117:6074-6082
    • (2011) Blood , vol.117 , pp. 6074-6082
    • Shaheen, M.1    Allen, C.2    Nickoloff, J.A.3    Hromas, R.4
  • 31
    • 84856738573 scopus 로고    scopus 로고
    • Enhanced killing of cancer cells by poly(ADP-ribose) polymerase inhibitors and topoisomerase i inhibitors reflects poisoning of both enzymes
    • 22158865 10.1074/jbc.M111.296475 1:CAS:528:DC%2BC38XhvVSjurs%3D
    • Patel AG, Flatten KS, Schneider PA, Dai NT, McDonald JS, Poirier GG, et al. (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
  • 32
    • 77955019276 scopus 로고    scopus 로고
    • Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and advanced breast cancer: A proof-of-concept trial
    • 20609467 10.1016/S0140-6736(10)60892-6 1:CAS:528:DC%2BC3cXpt1KktLc%3D
    • Tutt A, Robson M, Garber JE, Domchek SM, Audeh MW, Weitzel JN, et al. (2010) Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and advanced breast cancer: a proof-of-concept trial. Lancet 376:235-244
    • (2010) Lancet , vol.376 , pp. 235-244
    • Tutt, A.1    Robson, M.2    Garber, J.E.3    Domchek, S.M.4    Audeh, M.W.5    Weitzel, J.N.6
  • 33
    • 55949092708 scopus 로고    scopus 로고
    • High sensitivity of BRCA1-deficient mammary tumors to the PARP inhibitor AZD2281 alone and in combination with platinum drugs
    • 18971340 10.1073/pnas.0806092105 1:CAS:528:DC%2BD1cXhtlKlsr7F
    • Rottenberg S, Jaspers JE, Kersbergen A, van der Burg E, Nygren AO, Zander SA, et al. (2008) High sensitivity of BRCA1-deficient mammary tumors to the PARP inhibitor AZD2281 alone and in combination with platinum drugs. Proc Natl Acad Sci USA 105:17079-17084
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 17079-17084
    • Rottenberg, S.1    Jaspers, J.E.2    Kersbergen, A.3    Van Der Burg, E.4    Nygren, A.O.5    Zander, S.A.6
  • 34
    • 77954032829 scopus 로고    scopus 로고
    • Poly(ADP)-ribose polymerase inhibition: Frequent durable responses in BRCA carrier ovarian cancer correlating with platinum-free interval
    • 10.1200/JCO.2009.26.9589
    • Fong PC, Yap TA, Boss DS, Carden CP, Mergui-Roelvink M, Gourley C, et al. (2009) Poly(ADP)-ribose polymerase inhibition: frequent durable responses in BRCA carrier ovarian cancer correlating with platinum-free interval. J Clin Oncol 28:2512-2519
    • (2009) 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
  • 35
    • 67650471685 scopus 로고    scopus 로고
    • Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers
    • 19553641 10.1056/NEJMoa0900212 1:CAS:528:DC%2BD1MXosVKrtrw%3D
    • Fong PC, Boss DS, Yap TA, Tutt A, Wu P, Mergui-Roelvink M, et al. (2009) Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers. N Engl J Med 361:123-134
    • (2009) N Engl J Med , vol.361 , pp. 123-134
    • Fong, P.C.1    Boss, D.S.2    Yap, T.A.3    Tutt, A.4    Wu, P.5    Mergui-Roelvink, M.6
  • 36
    • 17244373777 scopus 로고    scopus 로고
    • Targeting the DNA repair defect in BRCA mutant cells as a therapeutic strategy
    • 15829967 10.1038/nature03445 1:CAS:528:DC%2BD2MXjtFOmsrc%3D
    • Farmer H, McCabe N, Lord CJ, Tutt AN, Johnson DA, Richardson TB, 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
  • 37
    • 79951887369 scopus 로고    scopus 로고
    • Therapeutic potential of Poly(ADP-ribose) polymerase inhibitor AG014699 in human cancers with mutated or methylated BRCA1 or BRCA2
    • 21183737 10.1093/jnci/djq509
    • Drew Y, Mulligan EA, Vong WT, Thomas HD, Kahn S, Kyle S, et al. (2010) Therapeutic potential of Poly(ADP-ribose) polymerase inhibitor AG014699 in human cancers with mutated or methylated BRCA1 or BRCA2. J Natl Cancer Inst 103:334-346
    • (2010) J Natl Cancer Inst , vol.103 , pp. 334-346
    • Drew, Y.1    Mulligan, E.A.2    Vong, W.T.3    Thomas, H.D.4    Kahn, S.5    Kyle, S.6
  • 38
    • 17244375049 scopus 로고    scopus 로고
    • Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase
    • 15829966 10.1038/nature03443 1:CAS:528:DC%2BD2MXjtFOmsrY%3D
    • Bryant HE, Schultz N, Thomas HD, Parker KM, Flower D, Lopez E, et al. (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
  • 39
    • 79951887369 scopus 로고    scopus 로고
    • Therapeutic Potential of Poly(ADP-ribose) Polymerase Inhibitor AG014699 in Human Cancers with Mutated or Methylated BRCA1 or BRCA2
    • 21183737 10.1093/jnci/djq509 1:CAS:528:DC%2BC3MXitlejsL0%3D
    • Drew Y, Mulligan EA, Vong W-T, Thomas HD, Kahn S, Kyle S, et al. (2011) Therapeutic Potential of Poly(ADP-ribose) Polymerase Inhibitor AG014699 in Human Cancers With Mutated or Methylated BRCA1 or BRCA2. J Natl Cancer Inst 103:334-346
    • (2011) J Natl Cancer Inst , vol.103 , pp. 334-346
    • Drew, Y.1    Mulligan, E.A.2    Vong, W.-T.3    Thomas, H.D.4    Kahn, S.5    Kyle, S.6
  • 40
    • 82955162712 scopus 로고    scopus 로고
    • Camptothecin induces p53-dependent and -independent apoptogenic signaling in melanoma cells
    • 10.1007/s10495-011-0635-8
    • Rudolf E, Rudolf K, Cervinka M (2011) Camptothecin induces p53-dependent and -independent apoptogenic signaling in melanoma cells. Apoptosis 16:1-12
    • (2011) Apoptosis , vol.16 , pp. 1-12
    • Rudolf, E.1    Rudolf, K.2    Cervinka, M.3
  • 41
    • 77951909740 scopus 로고    scopus 로고
    • ATM- and ATR-mediated response to DNA damage induced by a novel camptothecin, ST1968
    • 20042274 10.1016/j.canlet.2009.12.001 1:CAS:528:DC%2BC3cXkvFemtrs%3D
    • Zuco V, Benedetti V, Zunino F (2010) ATM- and ATR-mediated response to DNA damage induced by a novel camptothecin, ST1968. Cancer Lett 292:186-196
    • (2010) Cancer Lett , vol.292 , pp. 186-196
    • Zuco, V.1    Benedetti, V.2    Zunino, F.3
  • 42
    • 22844445482 scopus 로고    scopus 로고
    • Development of cell cycle active drugs for the treatment of gastrointestinal cancers: A new approach to cancer therapy
    • 16002840 10.1200/JCO.2005.18.341 1:CAS:528:DC%2BD2MXnsl2ks7Y%3D
    • Schwartz GK (2005) Development of cell cycle active drugs for the treatment of gastrointestinal cancers: a new approach to cancer therapy. J Clin Oncol 23:4499-4508
    • (2005) J Clin Oncol , vol.23 , pp. 4499-4508
    • Schwartz, G.K.1
  • 43
    • 0032731528 scopus 로고    scopus 로고
    • Schedule-dependent cytotoxicity of SN-38 in p53 wild-type and mutant colon adenocarcinoma cell lines
    • 10.1038/sj.bjc.6694370 1:CAS:528:DC%2BD3cXls1Kltw%3D%3D
    • Poele RH, Joel SP (1999) Schedule-dependent cytotoxicity of SN-38 in p53 wild-type and mutant colon adenocarcinoma cell lines. Br J Cancer 81:1285-93
    • (1999) Br J Cancer , vol.81 , pp. 1285-1293
    • Poele, R.H.1    Joel, S.P.2
  • 44
    • 84860390122 scopus 로고    scopus 로고
    • The Poly(ADP-ribose) polymerases (PARPs): New roles in intracellular transport
    • 10.1016/j.cellsig.2011.07.019
    • Elmageed A, Zakaria Y, Amarjit NS, Errami Y, Zerfaoui M (2012) The Poly(ADP-ribose) polymerases (PARPs): New roles in intracellular transport. Cell Signal 24:1-8
    • (2012) Cell Signal , vol.24 , pp. 1-8
    • Elmageed, A.1    Zakaria, Y.2    Amarjit, N.S.3    Errami, Y.4    Zerfaoui, M.5
  • 45
    • 84861907790 scopus 로고    scopus 로고
    • Enhanced cytotoxicity of PARP inhibition in mantle cell lymphoma harbouring mutations in both ATM and p53
    • 22416035 10.1002/emmm.201200229 1:CAS:528:DC%2BC38XnvFOnu7Y%3D
    • Williamson CT, Kubota E, Hamill JD, Klimowicz A, Ye R, Muzik H, et al. (2012) Enhanced cytotoxicity of PARP inhibition in mantle cell lymphoma harbouring mutations in both ATM and p53. EMBO Mol Med 4:515-527
    • (2012) EMBO Mol Med , vol.4 , pp. 515-527
    • Williamson, C.T.1    Kubota, E.2    Hamill, J.D.3    Klimowicz, A.4    Ye, R.5    Muzik, H.6
  • 46
    • 53149119164 scopus 로고    scopus 로고
    • Interaction between PARP-1 and ATR in mouse fibroblasts is blocked by PARP inhibition
    • 18691676 10.1016/j.dnarep.2008.07.006 1:CAS:528:DC%2BD1cXht1ensLvN
    • Kedar PS, Stefanick DF, Horton JK, Wilson SH (2008) Interaction between PARP-1 and ATR in mouse fibroblasts is blocked by PARP inhibition. DNA Repair 7:1787-1798
    • (2008) DNA Repair , vol.7 , pp. 1787-1798
    • Kedar, P.S.1    Stefanick, D.F.2    Horton, J.K.3    Wilson, S.H.4
  • 47
    • 82855182000 scopus 로고    scopus 로고
    • Poly(ADP-ribose) polymerase inhibition enhances p53-dependent and -independent DNA damage responses induced by DNA damaging agent
    • 22101337 10.4161/cc.10.23.18170 1:CAS:528:DC%2BC38XhsV2mt7w%3D
    • Nguyen D, Zajac-Kaye M, Rubinstein L, Voeller D, Tomaszewski JE, Kummar S, et al. (2011) Poly(ADP-ribose) polymerase inhibition enhances p53-dependent and -independent DNA damage responses induced by DNA damaging agent. Cell Cycle 10:4074-4082
    • (2011) Cell Cycle , vol.10 , pp. 4074-4082
    • Nguyen, D.1    Zajac-Kaye, M.2    Rubinstein, L.3    Voeller, D.4    Tomaszewski, J.E.5    Kummar, S.6
  • 48
    • 84879550836 scopus 로고    scopus 로고
    • Phase i study of the safety, pharmacokinetics (PK), and pharmacodynamics (PD) of the poly(ADP-ribose) polymerase (PARP) inhibitor veliparib (ABT-888; V) in combination with irinotecan (CPT-11; Ir) in patients (pts) with advanced solid tumors
    • 2011 April 2-6; Orlando, FL. Philidelphia, PA: American Association of Cancer Research
    • LoRusso JJ, Heilbrun LK, Shapiro G, Sausville EA, Boerner SA, Smith DW, et al. (2011) Phase I study of the safety, pharmacokinetics (PK), and pharmacodynamics (PD) of the poly(ADP-ribose) polymerase (PARP) inhibitor veliparib (ABT-888; V) in combination with irinotecan (CPT-11; Ir) in patients (pts) with advanced solid tumors. Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research; 2011 April 2-6; Orlando, FL. Philidelphia, PA: American Association of Cancer Research
    • (2011) Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research
    • Lorusso, J.J.1    Heilbrun, L.K.2    Shapiro, G.3    Sausville, E.A.4    Boerner, S.A.5    Smith, D.W.6


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