메뉴 건너뛰기




Volumn 59, Issue 21, 2016, Pages 9575-9598

An update on poly(ADP-ribose)polymerase-1 (PARP-1) inhibitors: Opportunities and challenges in cancer therapy

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; DNA; LACTAM; NICOTINAMIDE; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE 1; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE 2; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE INHIBITOR; TUMOR MARKER; PARP1 PROTEIN, HUMAN;

EID: 84994908887     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/acs.jmedchem.6b00055     Document Type: Review
Times cited : (188)

References (178)
  • 1
    • 77953764486 scopus 로고    scopus 로고
    • Evolution of poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors. from concept to clinic
    • Ferraris, D. V. Evolution of poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors. From concept to clinic J. Med. Chem. 2010, 53, 4561-4584 10.1021/jm100012m
    • (2010) J. Med. Chem. , vol.53 , pp. 4561-4584
    • Ferraris, D.V.1
  • 2
    • 33745011842 scopus 로고    scopus 로고
    • Emerging cancer therapeutic opportunities target DNA-repair systems
    • Ding, J.; Miao, Z. H.; Meng, L. H.; Geng, M. Y. Emerging cancer therapeutic opportunities target DNA-repair systems Trends Pharmacol. Sci. 2006, 27, 338-344 10.1016/j.tips.2006.04.007
    • (2006) Trends Pharmacol. Sci. , vol.27 , pp. 338-344
    • Ding, J.1    Miao, Z.H.2    Meng, L.H.3    Geng, M.Y.4
  • 3
    • 77956380540 scopus 로고    scopus 로고
    • Poly(ADP-ribose) polymerase inhibitors as promising cancer therapeutics
    • He, J. X.; Yang, C. H.; Miao, Z. H. Poly(ADP-ribose) polymerase inhibitors as promising cancer therapeutics Acta Pharmacol. Sin. 2010, 31, 1172-1180 10.1038/aps.2010.103
    • (2010) Acta Pharmacol. Sin. , vol.31 , pp. 1172-1180
    • He, J.X.1    Yang, C.H.2    Miao, Z.H.3
  • 4
    • 84903278353 scopus 로고    scopus 로고
    • New PARP targets for cancer therapy
    • Vyas, S.; Chang, P. New PARP targets for cancer therapy Nat. Rev. Cancer 2014, 14, 502-509 10.1038/nrc3748
    • (2014) Nat. Rev. Cancer , vol.14 , pp. 502-509
    • Vyas, S.1    Chang, P.2
  • 5
    • 84896886436 scopus 로고    scopus 로고
    • Review of poly (ADP-ribose) polymerase (PARP) mechanisms of action and rationale for targeting in cancer and other diseases
    • Morales, J.; Li, L.; Fattah, F. J.; Dong, Y.; Bey, E. A.; Patel, M.; Gao, J.; Boothman, D. A. Review of poly (ADP-ribose) polymerase (PARP) mechanisms of action and rationale for targeting in cancer and other diseases Crit. Rev. Eukaryotic Gene Expression 2014, 24, 15-28 10.1615/CritRevEukaryotGeneExpr.2013006875
    • (2014) Crit. Rev. Eukaryotic Gene Expression , vol.24 , pp. 15-28
    • Morales, J.1    Li, L.2    Fattah, F.J.3    Dong, Y.4    Bey, E.A.5    Patel, M.6    Gao, J.7    Boothman, D.A.8
  • 6
    • 84924262796 scopus 로고    scopus 로고
    • An update on PARP inhibitors for the treatment of cancer
    • Benafif, S.; Hall, M. An update on PARP inhibitors for the treatment of cancer OncoTargets Ther. 2015, 8, 519-528 10.2147/OTT.S30793
    • (2015) OncoTargets Ther. , vol.8 , pp. 519-528
    • Benafif, S.1    Hall, M.2
  • 11
    • 0029089917 scopus 로고
    • Potential chemotherapeutic activity of 4-iodo-3-nitrobenzamide. Metabolic reduction to the 3-nitroso derivative and induction of cell death in tumor cells in culture
    • Mendeleyev, J.; Kirsten, E.; Hakam, A.; Buki, K. G.; Kun, E. Potential chemotherapeutic activity of 4-iodo-3-nitrobenzamide. Metabolic reduction to the 3-nitroso derivative and induction of cell death in tumor cells in culture Biochem. Pharmacol. 1995, 50, 705-714 10.1016/0006-2952(95)00189-7
    • (1995) Biochem. Pharmacol. , vol.50 , pp. 705-714
    • Mendeleyev, J.1    Kirsten, E.2    Hakam, A.3    Buki, K.G.4    Kun, E.5
  • 20
    • 34548072788 scopus 로고    scopus 로고
    • The selective poly(ADP-ribose) polymerase-1(2) inhibitor, CEP-8983, increases the sensitivity of chemoresistant tumor cells to Temozolomide and irinotecan but does not potentiate myelotoxicity
    • Miknyoczki, S.; Chang, H.; Grobelny, J.; Pritchard, S.; Worrell, C.; McGann, N.; Ator, M.; Husten, J.; Deibold, J.; Hudkins, R.; Zulli, A.; Parchment, R.; Ruggeri, B. The selective poly(ADP-ribose) polymerase-1(2) inhibitor, CEP-8983, increases the sensitivity of chemoresistant tumor cells to Temozolomide and irinotecan but does not potentiate myelotoxicity Mol. Cancer Ther. 2007, 6, 2290-2302 10.1158/1535-7163.MCT-07-0062
    • (2007) Mol. Cancer Ther. , vol.6 , pp. 2290-2302
    • Miknyoczki, S.1    Chang, H.2    Grobelny, J.3    Pritchard, S.4    Worrell, C.5    McGann, N.6    Ator, M.7    Husten, J.8    Deibold, J.9    Hudkins, R.10    Zulli, A.11    Parchment, R.12    Ruggeri, B.13
  • 21
    • 84908181093 scopus 로고    scopus 로고
    • Another ″string to the bow″ of PJ34, a potent poly(ADP-Ribose)polymerase inhibitor: An antiplatelet effect through P2Y12 antagonism?
    • Lechaftois, M.; Dreano, E.; Palmier, B.; Margaill, I.; Marchand-Leroux, C.; Bachelot-Loza, C.; Lerouet, D. Another ″string to the bow″ of PJ34, a potent poly(ADP-Ribose)polymerase inhibitor: an antiplatelet effect through P2Y12 antagonism? PLoS One 2014, 9, e110776 10.1371/journal.pone.0110776
    • (2014) PLoS One , vol.9 , pp. e110776
    • Lechaftois, M.1    Dreano, E.2    Palmier, B.3    Margaill, I.4    Marchand-Leroux, C.5    Bachelot-Loza, C.6    Lerouet, D.7
  • 23
    • 84954563985 scopus 로고    scopus 로고
    • An open-label, dose-escalation study to evaluate the safety and pharmacokinetics of CEP-9722 (a PARP-1 and PARP-2 inhibitor) in combination with gemcitabine and cisplatin in patients with advanced solid tumors
    • Awada, A.; Campone, M.; Varga, A.; Aftimos, P.; Frenel, J. S.; Bahleda, R.; Gombos, A.; Bourbouloux, E.; Soria, J. C. An open-label, dose-escalation study to evaluate the safety and pharmacokinetics of CEP-9722 (a PARP-1 and PARP-2 inhibitor) in combination with gemcitabine and cisplatin in patients with advanced solid tumors Anti-Cancer Drugs 2016, 27, 342-348 10.1097/CAD.0000000000000336
    • (2016) Anti-Cancer Drugs , vol.27 , pp. 342-348
    • Awada, A.1    Campone, M.2    Varga, A.3    Aftimos, P.4    Frenel, J.S.5    Bahleda, R.6    Gombos, A.7    Bourbouloux, E.8    Soria, J.C.9
  • 26
    • 84928501238 scopus 로고    scopus 로고
    • Niraparib: A Poly(ADP-ribose) polymerase (PARP) inhibitor for the treatment of tumors with defective homologous recombination
    • Jones, P.; Wilcoxen, K.; Rowley, M.; Toniatti, C. Niraparib: A Poly(ADP-ribose) polymerase (PARP) inhibitor for the treatment of tumors with defective homologous recombination J. Med. Chem. 2015, 58, 3302-3314 10.1021/jm5018237
    • (2015) J. Med. Chem. , vol.58 , pp. 3302-3314
    • Jones, P.1    Wilcoxen, K.2    Rowley, M.3    Toniatti, C.4
  • 28
    • 84955157633 scopus 로고    scopus 로고
    • Discovery and characterization of (8S, 9R)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1H-1, 2, 4-triazol-5-yl)-2, 7, 8, 9-tetrahydro-3H-pyrido [4, 3, 2-de] phthalazin-3-one (BMN 673, talazoparib), a novel, highly potent, and orally efficacious poly (ADP-ribose) polymerase-1/2 inhibitor as an anticancer agent
    • Wang, B.; Chu, D.; Feng, Y.; Shen, Y.; Aoyagi-Scharber, M.; Post, L. E. Discovery and characterization of (8S, 9R)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1H-1, 2, 4-triazol-5-yl)-2, 7, 8, 9-tetrahydro-3H-pyrido [4, 3, 2-de] phthalazin-3-one (BMN 673, talazoparib), a novel, highly potent, and orally efficacious poly (ADP-ribose) polymerase-1/2 inhibitor as an anticancer agent J. Med. Chem. 2016, 59, 335-357 10.1021/acs.jmedchem.5b01498
    • (2016) J. Med. Chem. , vol.59 , pp. 335-357
    • Wang, B.1    Chu, D.2    Feng, Y.3    Shen, Y.4    Aoyagi-Scharber, M.5    Post, L.E.6
  • 35
    • 79955589677 scopus 로고    scopus 로고
    • A phase i study to determine the comparative bioavailability of two different oral formulations of the PARP inhibitor, olaparib (AZD2281), in patients with advanced solid tumors
    • Molife, L. R.; Forster, M. D.; Krebs, M.; Pwint, T.; Middleton, M. R.; Kaye, S. B.; McCormack, P.; Swaisland, H.; Carmichael, J.; Ranson, M. A phase I study to determine the comparative bioavailability of two different oral formulations of the PARP inhibitor, olaparib (AZD2281), in patients with advanced solid tumors J. Clin. Oncol. 2010, 28 (15 suppl) 2599
    • (2010) J. Clin. Oncol. , vol.28 , Issue.15 , pp. 2599
    • Molife, L.R.1    Forster, M.D.2    Krebs, M.3    Pwint, T.4    Middleton, M.R.5    Kaye, S.B.6    McCormack, P.7    Swaisland, H.8    Carmichael, J.9    Ranson, M.10
  • 36
    • 84880918621 scopus 로고    scopus 로고
    • Evaluation of the pharmacodynamics and pharmacokinetics of the PARP inhibitor olaparib: A Phase i multicentre trial in patients scheduled for elective breast cancer surgery
    • Bundred, N.; Gardovskis, J.; Jaskiewicz, J.; Eglitis, J.; Paramonov, V.; McCormack, P.; Swaisland, H.; Cavallin, M.; Parry, T.; Carmichael, J.; Dixon, J. M. Evaluation of the pharmacodynamics and pharmacokinetics of the PARP inhibitor olaparib: a Phase I multicentre trial in patients scheduled for elective breast cancer surgery Invest. New Drugs 2013, 31, 949-958 10.1007/s10637-012-9922-7
    • (2013) Invest. New Drugs , vol.31 , pp. 949-958
    • Bundred, N.1    Gardovskis, J.2    Jaskiewicz, J.3    Eglitis, J.4    Paramonov, V.5    McCormack, P.6    Swaisland, H.7    Cavallin, M.8    Parry, T.9    Carmichael, J.10    Dixon, J.M.11
  • 39
    • 84863010984 scopus 로고    scopus 로고
    • Phase II, open-label, randomized, multicenter study comparing the efficacy and safety of olaparib, a poly (ADP-ribose) polymerase inhibitor, and pegylated liposomal doxorubicin in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer
    • Kaye, S. B.; Lubinski, J.; Matulonis, U.; Ang, J. E.; Gourley, C.; Karlan, B. Y.; Amnon, A.; Bell-McGuinn, K. M.; Chen, L. M.; Friedlander, M.; Safra, T.; Vergote, I.; Wickens, M.; Lowe, E. S.; Carmichael, J.; Kaufman, B. Phase II, open-label, randomized, multicenter study comparing the efficacy and safety of olaparib, a poly (ADP-ribose) polymerase inhibitor, and pegylated liposomal doxorubicin in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer J. Clin. Oncol. 2012, 30, 372-379 10.1200/JCO.2011.36.9215
    • (2012) J. Clin. Oncol. , vol.30 , pp. 372-379
    • Kaye, S.B.1    Lubinski, J.2    Matulonis, U.3    Ang, J.E.4    Gourley, C.5    Karlan, B.Y.6    Amnon, A.7    Bell-McGuinn, K.M.8    Chen, L.M.9    Friedlander, M.10    Safra, T.11    Vergote, I.12    Wickens, M.13    Lowe, E.S.14    Carmichael, J.15    Kaufman, B.16
  • 44
    • 84905183020 scopus 로고    scopus 로고
    • Phase i trial of olaparib in combination with cisplatin for the treatment of patients with advanced breast, ovarian and other solid tumors
    • Balmaña, J.; Tung, N. M.; Isakoff, S. J.; Graña, B.; Ryan, P. D.; Saura, C.; Lowe, E. S.; Frewer, P.; Winer, E.; Baselga, J.; Garber, J. E. Phase I trial of olaparib in combination with cisplatin for the treatment of patients with advanced breast, ovarian and other solid tumors Ann. Oncol. 2014, 25, 1656-1663 10.1093/annonc/mdu187
    • (2014) Ann. Oncol. , vol.25 , pp. 1656-1663
    • Balmaña, J.1    Tung, N.M.2    Isakoff, S.J.3    Graña, B.4    Ryan, P.D.5    Saura, C.6    Lowe, E.S.7    Frewer, P.8    Winer, E.9    Baselga, J.10    Garber, J.E.11
  • 47
    • 84866564290 scopus 로고    scopus 로고
    • Safety and tolerability of the poly(ADP-ribose) polymerase (PARP) inhibitor, olaparib (AZD2281) in combination with topotecan for the treatment of patients with advanced solid tumors: A phase i study
    • Samol, J.; Ranson, M.; Scott, E.; Macpherson, E.; Carmichael, J.; Thomas, A.; Cassidy, J. Safety and tolerability of the poly(ADP-ribose) polymerase (PARP) inhibitor, olaparib (AZD2281) in combination with topotecan for the treatment of patients with advanced solid tumors: a phase I study Invest. New Drugs 2012, 30, 1493-1500 10.1007/s10637-011-9682-9
    • (2012) Invest. New Drugs , vol.30 , pp. 1493-1500
    • Samol, J.1    Ranson, M.2    Scott, E.3    MacPherson, E.4    Carmichael, J.5    Thomas, A.6    Cassidy, J.7
  • 49
    • 84884509017 scopus 로고    scopus 로고
    • Phase i trial of the oral PARP inhibitor olaparib in combination with paclitaxel for first- or second-line treatment of patients with metastatic triple-negative breast cancer
    • Dent, R. A.; Lindeman, G. J.; Clemons, M.; Wildiers, H.; Chan, A.; McCarthy, N. J.; Singer, C. F.; Lowe, E. S.; Watkins, C. L.; Carmichael, J. Phase I trial of the oral PARP inhibitor olaparib in combination with paclitaxel for first- or second-line treatment of patients with metastatic triple-negative breast cancer Breast Cancer Res. 2013, 15, R88 10.1186/bcr3484
    • (2013) Breast Cancer Res. , vol.15 , pp. R88
    • Dent, R.A.1    Lindeman, G.J.2    Clemons, M.3    Wildiers, H.4    Chan, A.5    McCarthy, N.J.6    Singer, C.F.7    Lowe, E.S.8    Watkins, C.L.9    Carmichael, J.10
  • 50
    • 84994803905 scopus 로고    scopus 로고
    • Phase Ib/II with expansion of patients at the MTD study of olaparib plus weekly (metronomic) carboplatin and paclitaxel in relapsed ovarian cancer patients
    • Rivkin, S. E.; Iriarte, D.; Sloan, H.; Wiseman, C.; Moon, J. Phase Ib/II with expansion of patients at the MTD study of olaparib plus weekly (metronomic) carboplatin and paclitaxel in relapsed ovarian cancer patients J. Clin. Oncol. 2014, 32 (15 suppl) 5527
    • (2014) J. Clin. Oncol. , vol.32 , Issue.15 , pp. 5527
    • Rivkin, S.E.1    Iriarte, D.2    Sloan, H.3    Wiseman, C.4    Moon, J.5
  • 52
    • 84947795362 scopus 로고    scopus 로고
    • Randomized, double-blind phase II trial with prospective classification by ATM protein level to evaluate the efficacy and tolerability of olaparib plus paclitaxel in patients with recurrent or metastatic gastric cancer
    • Bang, Y. J.; Im, S. A.; Lee, K. W.; Cho, J. Y.; Song, E. K.; Lee, K. H.; Kim, Y. H.; Park, J. O.; Chun, H. G.; Zang, D. Y.; Fielding, A.; Rowbottom, J.; Hodgson, D.; O'Connor, M. J.; Yin, X.; Kim, W. H. Randomized, double-blind phase II trial with prospective classification by ATM protein level to evaluate the efficacy and tolerability of olaparib plus paclitaxel in patients with recurrent or metastatic gastric cancer J. Clin. Oncol. 2015, 33, 3858-3865 10.1200/JCO.2014.60.0320
    • (2015) J. Clin. Oncol. , vol.33 , pp. 3858-3865
    • Bang, Y.J.1    Im, S.A.2    Lee, K.W.3    Cho, J.Y.4    Song, E.K.5    Lee, K.H.6    Kim, Y.H.7    Park, J.O.8    Chun, H.G.9    Zang, D.Y.10    Fielding, A.11    Rowbottom, J.12    Hodgson, D.13    O'Connor, M.J.14    Yin, X.15    Kim, W.H.16
  • 53
    • 84856509572 scopus 로고    scopus 로고
    • Phase i study to assess the safety and tolerability of olaparib in combination with bevacizumab in patients with advanced solid tumours
    • Dean, E.; Middleton, M. R.; Pwint, T.; Swaisland, H.; Carmichael, J.; Goodege-Kunwar, P.; Ranson, M. Phase I study to assess the safety and tolerability of olaparib in combination with bevacizumab in patients with advanced solid tumours Br. J. Cancer 2012, 106, 468-474 10.1038/bjc.2011.555
    • (2012) Br. J. Cancer , vol.106 , pp. 468-474
    • Dean, E.1    Middleton, M.R.2    Pwint, T.3    Swaisland, H.4    Carmichael, J.5    Goodege-Kunwar, P.6    Ranson, M.7
  • 54
    • 84883054717 scopus 로고    scopus 로고
    • A Phase 1 trial of the poly(ADP-ribose) polymerase inhibitor olaparib (AZD2281) in combination with the anti-angiogenic cediranib (AZD2171) in recurrent epithelial ovarian or triple-negative breast cancer
    • Liu, J. F.; Tolaney, S. M.; Birrer, M.; Fleming, G. F.; Buss, M. K.; Dahlberg, S. E.; Lee, H.; Whalen, C.; Tyburski, K.; Winer, E.; Ivy, P.; Matulonis, U. A. A Phase 1 trial of the poly(ADP-ribose) polymerase inhibitor olaparib (AZD2281) in combination with the anti-angiogenic cediranib (AZD2171) in recurrent epithelial ovarian or triple-negative breast cancer Eur. J. Cancer 2013, 49, 2972-2978 10.1016/j.ejca.2013.05.020
    • (2013) Eur. J. Cancer , vol.49 , pp. 2972-2978
    • Liu, J.F.1    Tolaney, S.M.2    Birrer, M.3    Fleming, G.F.4    Buss, M.K.5    Dahlberg, S.E.6    Lee, H.7    Whalen, C.8    Tyburski, K.9    Winer, E.10    Ivy, P.11    Matulonis, U.A.12
  • 57
    • 84994896364 scopus 로고    scopus 로고
    • Phase Ib study to evaluate the efficacy and tolerability of olaparib (AZD2281) plus gefitinib in patients (P) with epidermal growth factor receptor (EGFR) mutation positive advanced non-small cell lung cancer (NSCLC) patients
    • Campelo, R. G.; Felip, E.; Massuti, B.; Majem, M.; Carcereny, E.; Palmero, R.; Molina-Vila, M. A.; Cajal, R.; Sanchez-Ronco, M.; Rosell, R. Phase Ib study to evaluate the efficacy and tolerability of olaparib (AZD2281) plus gefitinib in patients (P) with epidermal growth factor receptor (EGFR) mutation positive advanced non-small cell lung cancer (NSCLC) patients J. Clin. Oncol. 2014, 32 (15 suppl) 8079
    • (2014) J. Clin. Oncol. , vol.32 , Issue.15 , pp. 8079
    • Campelo, R.G.1    Felip, E.2    Massuti, B.3    Majem, M.4    Carcereny, E.5    Palmero, R.6    Molina-Vila, M.A.7    Cajal, R.8    Sanchez-Ronco, M.9    Rosell, R.10
  • 61
    • 84929440309 scopus 로고    scopus 로고
    • Poly (ADP-ribose) polymerase inhibitors: Recent advances and future development
    • Scott, C. L.; Swisher, E. M.; Kaufmann, S. H. Poly (ADP-ribose) polymerase inhibitors: recent advances and future development J. Clin. Oncol. 2015, 33, 1397-1406 10.1200/JCO.2014.58.8848
    • (2015) J. Clin. Oncol. , vol.33 , pp. 1397-1406
    • Scott, C.L.1    Swisher, E.M.2    Kaufmann, S.H.3
  • 64
    • 84901218339 scopus 로고    scopus 로고
    • 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, J. H.; Pommier, Y. 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. 2014, 349, 408-416 10.1124/jpet.113.210146
    • (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
  • 66
    • 84881519427 scopus 로고    scopus 로고
    • Resistance to PARP-inhibitors in cancer therapy
    • Montoni, A.; Robu, M.; Pouliot, E.; Shah, G. M. Resistance to PARP-inhibitors in cancer therapy Front. Pharmacol. 2013, 4, 18 10.3389/fphar.2013.00018
    • (2013) Front. Pharmacol. , vol.4 , pp. 18
    • Montoni, A.1    Robu, M.2    Pouliot, E.3    Shah, G.M.4
  • 68
    • 84923090502 scopus 로고    scopus 로고
    • Mammalian polymerase promotes alternative NHEJ and suppresses recombination
    • Mateos-Gomez, P. A.; Gong, F.; Nair, N.; Miller, K. M.; Lazzerini-Denchi, E.; Sfeir, A. Mammalian polymerase promotes alternative NHEJ and suppresses recombination Nature 2015, 518, 254-257 10.1038/nature14157
    • (2015) Nature , vol.518 , pp. 254-257
    • Mateos-Gomez, P.A.1    Gong, F.2    Nair, N.3    Miller, K.M.4    Lazzerini-Denchi, E.5    Sfeir, A.6
  • 70
    • 84925815358 scopus 로고    scopus 로고
    • New facets in the regulation of gene expression by ADP-ribosylation and poly(ADP-ribose) polymerases
    • Ryu, K. W.; Kim, D. S.; Kraus, W. L. New facets in the regulation of gene expression by ADP-ribosylation and poly(ADP-ribose) polymerases Chem. Rev. 2015, 115, 2453-2481 10.1021/cr5004248
    • (2015) Chem. Rev. , vol.115 , pp. 2453-2481
    • Ryu, K.W.1    Kim, D.S.2    Kraus, W.L.3
  • 72
    • 84886719040 scopus 로고    scopus 로고
    • PARP-1 and gene regulation: Progress and puzzles
    • Kraus, W. L.; Hottiger, M. O. PARP-1 and gene regulation: progress and puzzles Mol. Aspects Med. 2013, 34, 1109-1123 10.1016/j.mam.2013.01.005
    • (2013) Mol. Aspects Med. , vol.34 , pp. 1109-1123
    • Kraus, W.L.1    Hottiger, M.O.2
  • 73
    • 84940576834 scopus 로고    scopus 로고
    • BRACAnalysis CDx as a companion diagnostic tool for Lynparza
    • Gunderson, C. C.; Moore, K. N. BRACAnalysis CDx as a companion diagnostic tool for Lynparza Expert Rev. Mol. Diagn. 2015, 15, 1111-1116 10.1586/14737159.2015.1078238
    • (2015) Expert Rev. Mol. Diagn. , vol.15 , pp. 1111-1116
    • Gunderson, C.C.1    Moore, K.N.2
  • 74
    • 79959838081 scopus 로고    scopus 로고
    • Integrated genomic analyses of ovarian carcinoma
    • The Cancer Genome Atlas Research Network
    • The Cancer Genome Atlas Research Network. Integrated genomic analyses of ovarian carcinoma. Nature 2011, 474, 609-615. 10.1038/nature10166
    • (2011) Nature , vol.474 , pp. 609-615
  • 76
    • 84941025055 scopus 로고    scopus 로고
    • Recruitment and activation of the ATM kinase in the absence of DNA-damage sensors
    • Hartlerode, A. J.; Morgan, M. J.; Wu, Y.; Buis, J.; Ferguson, D. O. Recruitment and activation of the ATM kinase in the absence of DNA-damage sensors Nat. Struct. Mol. Biol. 2015, 22, 736-743 10.1038/nsmb.3072
    • (2015) Nat. Struct. Mol. Biol. , vol.22 , pp. 736-743
    • Hartlerode, A.J.1    Morgan, M.J.2    Wu, Y.3    Buis, J.4    Ferguson, D.O.5
  • 77
    • 78951474460 scopus 로고    scopus 로고
    • The MRE11 complex: Starting from the ends
    • Stracker, T. H.; Petrini, J. H. The MRE11 complex: starting from the ends Nat. Rev. Mol. Cell Biol. 2011, 12, 90-103 10.1038/nrm3047
    • (2011) Nat. Rev. Mol. Cell Biol. , vol.12 , pp. 90-103
    • Stracker, T.H.1    Petrini, J.H.2
  • 82
    • 84925664415 scopus 로고    scopus 로고
    • ATM and ATR as therapeutic targets in cancer
    • Weber, A. M.; Ryan, A. J. ATM and ATR as therapeutic targets in cancer Pharmacol. Ther. 2015, 149, 124-138 10.1016/j.pharmthera.2014.12.001
    • (2015) Pharmacol. Ther. , vol.149 , pp. 124-138
    • Weber, A.M.1    Ryan, A.J.2
  • 83
    • 80055108191 scopus 로고    scopus 로고
    • Chk2 deficiency in Myc overexpressing lymphoma cells elicits a synergistic lethal response in combination with PARP inhibition
    • Hoglund, A.; Stromvall, K.; Li, Y.; Forshell, L. P.; Nilsson, J. A. Chk2 deficiency in Myc overexpressing lymphoma cells elicits a synergistic lethal response in combination with PARP inhibition Cell Cycle 2011, 10, 3598-3607 10.4161/cc.10.20.17887
    • (2011) Cell Cycle , vol.10 , pp. 3598-3607
    • Hoglund, A.1    Stromvall, K.2    Li, Y.3    Forshell, L.P.4    Nilsson, J.A.5
  • 85
    • 84903707964 scopus 로고    scopus 로고
    • Low ATM protein expression and depletion of p53 correlates with olaparib sensitivity in gastric cancer cell lines
    • Kubota, E.; Williamson, C. T.; Ye, R.; Elegbede, A.; Peterson, L.; Lees-Miller, S. P.; Bebb, D. G. Low ATM protein expression and depletion of p53 correlates with olaparib sensitivity in gastric cancer cell lines Cell Cycle 2014, 13, 2129-2137 10.4161/cc.29212
    • (2014) Cell Cycle , vol.13 , pp. 2129-2137
    • Kubota, E.1    Williamson, C.T.2    Ye, R.3    Elegbede, A.4    Peterson, L.5    Lees-Miller, S.P.6    Bebb, D.G.7
  • 89
    • 84875247647 scopus 로고    scopus 로고
    • Epigenetic inactivation of BRCA1 through promoter hypermethylation in ovarian cancer progression
    • Wang, Y. Q.; Yan, Q.; Zhang, J. R.; Li, S. D.; Yang, Y. X.; Wan, X. P. Epigenetic inactivation of BRCA1 through promoter hypermethylation in ovarian cancer progression J. Obstet. Gynaecol. Res. 2013, 39, 549-554 10.1111/j.1447-0756.2012.01979.x
    • (2013) J. Obstet. Gynaecol. Res. , vol.39 , pp. 549-554
    • Wang, Y.Q.1    Yan, Q.2    Zhang, J.R.3    Li, S.D.4    Yang, Y.X.5    Wan, X.P.6
  • 94
    • 84922548577 scopus 로고    scopus 로고
    • Fanconi anemia repair pathway dysfunction, a potential therapeutic target in lung cancer
    • Duan, W.; Gao, L.; Aguila, B.; Kalvala, A.; Otterson, G. A.; Villalona-Calero, M. A. Fanconi anemia repair pathway dysfunction, a potential therapeutic target in lung cancer Front. Oncol. 2014, 4, 368 10.3389/fonc.2014.00368
    • (2014) Front. Oncol. , vol.4 , pp. 368
    • Duan, W.1    Gao, L.2    Aguila, B.3    Kalvala, A.4    Otterson, G.A.5    Villalona-Calero, M.A.6
  • 97
    • 84897457200 scopus 로고    scopus 로고
    • Ovarian cancer-associated mutations disable catalytic activity of CDK12, a kinase that promotes homologous recombination repair and resistance to cisplatin and poly(ADP-ribose) polymerase inhibitors
    • Joshi, P. M.; Sutor, S. L.; Huntoon, C. J.; Karnitz, L. M. Ovarian cancer-associated mutations disable catalytic activity of CDK12, a kinase that promotes homologous recombination repair and resistance to cisplatin and poly(ADP-ribose) polymerase inhibitors J. Biol. Chem. 2014, 289, 9247-9253 10.1074/jbc.M114.551143
    • (2014) J. Biol. Chem. , vol.289 , pp. 9247-9253
    • Joshi, P.M.1    Sutor, S.L.2    Huntoon, C.J.3    Karnitz, L.M.4
  • 101
    • 84863402644 scopus 로고    scopus 로고
    • Does PTEN loss impair DNA double-strand break repair by homologous recombination?
    • Hunt, C. R.; Gupta, A.; Horikoshi, N.; Pandita, T. K. Does PTEN loss impair DNA double-strand break repair by homologous recombination? Clin. Cancer Res. 2012, 18, 920-922 10.1158/1078-0432.CCR-11-3131
    • (2012) Clin. Cancer Res. , vol.18 , pp. 920-922
    • Hunt, C.R.1    Gupta, A.2    Horikoshi, N.3    Pandita, T.K.4
  • 102
    • 77956833348 scopus 로고    scopus 로고
    • Phosphatases in the cellular response to DNA damage
    • Freeman, A. K.; Monteiro, A. N. Phosphatases in the cellular response to DNA damage Cell Commun. Signaling 2010, 8, 27 10.1186/1478-811X-8-27
    • (2010) Cell Commun. Signaling , vol.8 , pp. 27
    • Freeman, A.K.1    Monteiro, A.N.2
  • 103
    • 84871198111 scopus 로고    scopus 로고
    • Loss of PPP2R2A inhibits homologous recombination DNA repair and predicts tumor sensitivity to PARP inhibition
    • Kalev, P.; Simicek, M.; Vazquez, I.; Munck, S.; Chen, L.; Soin, T.; Danda, N.; Chen, W.; Sablina, A. Loss of PPP2R2A inhibits homologous recombination DNA repair and predicts tumor sensitivity to PARP inhibition Cancer Res. 2012, 72, 6414-6424 10.1158/0008-5472.CAN-12-1667
    • (2012) Cancer Res. , vol.72 , pp. 6414-6424
    • Kalev, P.1    Simicek, M.2    Vazquez, I.3    Munck, S.4    Chen, L.5    Soin, T.6    Danda, N.7    Chen, W.8    Sablina, A.9
  • 106
    • 79957516181 scopus 로고    scopus 로고
    • EMSY overexpression disrupts the BRCA2/RAD51 pathway in the DNA-damage response: Implications for chromosomal instability/recombination syndromes as checkpoint diseases
    • Cousineau, I.; Belmaaza, A. EMSY overexpression disrupts the BRCA2/RAD51 pathway in the DNA-damage response: implications for chromosomal instability/recombination syndromes as checkpoint diseases Mol. Genet. Genomics 2011, 285, 325-340 10.1007/s00438-011-0612-5
    • (2011) Mol. Genet. Genomics , vol.285 , pp. 325-340
    • Cousineau, I.1    Belmaaza, A.2
  • 107
    • 84878831995 scopus 로고    scopus 로고
    • HP1 promotes tumor suppressor BRCA1 functions during the DNA damage response
    • Lee, Y. H.; Kuo, C. Y.; Stark, J. M.; Shih, H. M.; Ann, D. K. HP1 promotes tumor suppressor BRCA1 functions during the DNA damage response Nucleic Acids Res. 2013, 41, 5784-5798 10.1093/nar/gkt231
    • (2013) Nucleic Acids Res. , vol.41 , pp. 5784-5798
    • Lee, Y.H.1    Kuo, C.Y.2    Stark, J.M.3    Shih, H.M.4    Ann, D.K.5
  • 108
    • 84929492504 scopus 로고    scopus 로고
    • HP1beta is a biomarker for breast cancer prognosis and PARP inhibitor therapy
    • Lee, Y. H.; Liu, X.; Qiu, F.; O'Connor, T. R.; Yen, Y.; Ann, D. K. HP1beta is a biomarker for breast cancer prognosis and PARP inhibitor therapy PLoS One 2015, 10, e0121207 10.1371/journal.pone.0121207
    • (2015) PLoS One , vol.10 , pp. e0121207
    • Lee, Y.H.1    Liu, X.2    Qiu, F.3    O'Connor, T.R.4    Yen, Y.5    Ann, D.K.6
  • 109
    • 77953677649 scopus 로고    scopus 로고
    • Aurora-A expressing tumour cells are deficient for homology-directed DNA double strand-break repair and sensitive to PARP inhibition
    • Sourisseau, T.; Maniotis, D.; McCarthy, A.; Tang, C.; Lord, C. J.; Ashworth, A.; Linardopoulos, S. Aurora-A expressing tumour cells are deficient for homology-directed DNA double strand-break repair and sensitive to PARP inhibition EMBO Mol. Med. 2010, 2, 130-142 10.1002/emmm.201000068
    • (2010) EMBO Mol. Med. , vol.2 , pp. 130-142
    • Sourisseau, T.1    Maniotis, D.2    McCarthy, A.3    Tang, C.4    Lord, C.J.5    Ashworth, A.6    Linardopoulos, S.7
  • 110
    • 84887431012 scopus 로고    scopus 로고
    • Mechanisms of resistance to therapies targeting BRCA-mutant cancers
    • Lord, C. J.; Ashworth, A. Mechanisms of resistance to therapies targeting BRCA-mutant cancers Nat. Med. 2013, 19, 1381-1388 10.1038/nm.3369
    • (2013) Nat. Med. , vol.19 , pp. 1381-1388
    • Lord, C.J.1    Ashworth, A.2
  • 111
    • 84964312809 scopus 로고    scopus 로고
    • Molecular pathways: Targeting ETS gene fusions in cancer
    • Feng, F. Y.; Brenner, J. C.; Hussain, M.; Chinnaiyan, A. M. Molecular pathways: targeting ETS gene fusions in cancer Clin. Cancer Res. 2014, 20, 4442-4448 10.1158/1078-0432.CCR-13-0275
    • (2014) Clin. Cancer Res. , vol.20 , pp. 4442-4448
    • Feng, F.Y.1    Brenner, J.C.2    Hussain, M.3    Chinnaiyan, A.M.4
  • 115
    • 84959099909 scopus 로고    scopus 로고
    • Flavones inhibit breast cancer proliferation through the Akt/FOXO3a signaling pathway
    • Lin, C. H.; Chang, C. Y.; Lee, K. R.; Lin, H. J.; Chen, T. H.; Wan, L. Flavones inhibit breast cancer proliferation through the Akt/FOXO3a signaling pathway BMC Cancer 2015, 15, 958 10.1186/s12885-015-1965-7
    • (2015) BMC Cancer , vol.15 , pp. 958
    • Lin, C.H.1    Chang, C.Y.2    Lee, K.R.3    Lin, H.J.4    Chen, T.H.5    Wan, L.6
  • 116
    • 84953439235 scopus 로고    scopus 로고
    • Tumor suppressive effect of PARP1 and FOXO3A in gastric cancers and its clinical implications
    • Park, S. H.; Jang, K. Y.; Kim, M. J.; Yoon, S.; Jo, Y.; Kwon, S. M.; Kim, K. M.; Kwon, K. S.; Kim, C. Y.; Woo, H. G. Tumor suppressive effect of PARP1 and FOXO3A in gastric cancers and its clinical implications Oncotarget 2015, 6 (42) 44819-44831 10.18632/oncotarget.6264
    • (2015) Oncotarget , vol.6 , Issue.42 , pp. 44819-44831
    • Park, S.H.1    Jang, K.Y.2    Kim, M.J.3    Yoon, S.4    Jo, Y.5    Kwon, S.M.6    Kim, K.M.7    Kwon, K.S.8    Kim, C.Y.9    Woo, H.G.10
  • 120
    • 43249085571 scopus 로고    scopus 로고
    • A synthetic lethal siRNA screen identifying genes mediating sensitivity to a PARP inhibitor
    • Turner, N. C.; Lord, C. J.; Iorns, E.; Brough, R.; Swift, S.; Elliott, R.; Rayter, S.; Tutt, A. N.; Ashworth, A. A synthetic lethal siRNA screen identifying genes mediating sensitivity to a PARP inhibitor EMBO J. 2008, 27, 1368-1377 10.1038/emboj.2008.61
    • (2008) EMBO J. , vol.27 , pp. 1368-1377
    • Turner, N.C.1    Lord, C.J.2    Iorns, E.3    Brough, R.4    Swift, S.5    Elliott, R.6    Rayter, S.7    Tutt, A.N.8    Ashworth, A.9
  • 122
    • 84944909449 scopus 로고    scopus 로고
    • Cdk5 promotes DNA replication stress checkpoint activation through RPA-32 phosphorylation, and impacts on metastasis free survival in breast cancer patients
    • Chiker, S.; Pennaneach, V.; Loew, D.; Dingli, F.; Biard, D.; Cordelières, F. P.; Gemble, S.; Vacher, S.; Bieche, I.; Hall, J.; Fernet, M. Cdk5 promotes DNA replication stress checkpoint activation through RPA-32 phosphorylation, and impacts on metastasis free survival in breast cancer patients Cell Cycle 2015, 14, 3066-3078 10.1080/15384101.2015.1078020
    • (2015) Cell Cycle , vol.14 , pp. 3066-3078
    • Chiker, S.1    Pennaneach, V.2    Loew, D.3    Dingli, F.4    Biard, D.5    Cordelières, F.P.6    Gemble, S.7    Vacher, S.8    Bieche, I.9    Hall, J.10    Fernet, M.11
  • 125
    • 77955735085 scopus 로고    scopus 로고
    • Cdk5: Links to DNA damage
    • Huang, E.; Qu, D.; Park, D. S. Cdk5: Links to DNA damage Cell Cycle 2010, 9, 3142-3143 10.4161/cc.9.16.12955
    • (2010) Cell Cycle , vol.9 , pp. 3142-3143
    • Huang, E.1    Qu, D.2    Park, D.S.3
  • 126
    • 84921367731 scopus 로고    scopus 로고
    • Synthetic lethality and cancer therapy: Lessons learned from the development of PARP inhibitors
    • Lord, C. J.; Tutt, A. N.; Ashworth, A. Synthetic lethality and cancer therapy: lessons learned from the development of PARP inhibitors Annu. Rev. Med. 2015, 66, 455-470 10.1146/annurev-med-050913-022545
    • (2015) Annu. Rev. Med. , vol.66 , pp. 455-470
    • Lord, C.J.1    Tutt, A.N.2    Ashworth, A.3
  • 127
    • 84939175214 scopus 로고    scopus 로고
    • PARP inhibitors in the management of breast cancer: Current data and future prospects
    • Livraghi, L.; Garber, J. E. PARP inhibitors in the management of breast cancer: current data and future prospects BMC Med. 2015, 13, 188 10.1186/s12916-015-0425-1
    • (2015) BMC Med. , vol.13 , pp. 188
    • Livraghi, L.1    Garber, J.E.2
  • 128
    • 84893517261 scopus 로고    scopus 로고
    • Molecular pathways: How can BRCA-mutated tumors become resistant to PARP inhibitors?
    • Bouwman, P.; Jonkers, J. Molecular pathways: how can BRCA-mutated tumors become resistant to PARP inhibitors? Clin. Cancer Res. 2014, 20, 540-547 10.1158/1078-0432.CCR-13-0225
    • (2014) Clin. Cancer Res. , vol.20 , pp. 540-547
    • Bouwman, P.1    Jonkers, J.2
  • 133
    • 84902076522 scopus 로고    scopus 로고
    • Phosphorylation of ribosomal protein S6 confers PARP inhibitor resistance in BRCA1-deficient cancers
    • Sun, C. K.; Zhang, F.; Xiang, T.; Chen, Q.; Pandita, T. K.; Huang, Y.; Hu, M. C.; Yang, Q. Phosphorylation of ribosomal protein S6 confers PARP inhibitor resistance in BRCA1-deficient cancers Oncotarget 2014, 5, 3375-3385 10.18632/oncotarget.1952
    • (2014) Oncotarget , vol.5 , pp. 3375-3385
    • Sun, C.K.1    Zhang, F.2    Xiang, T.3    Chen, Q.4    Pandita, T.K.5    Huang, Y.6    Hu, M.C.7    Yang, Q.8
  • 139
    • 84938633101 scopus 로고    scopus 로고
    • BCRP and P-gp relay overexpression in triple negative basal-like breast cancer cell line: A prospective role in resistance to Olaparib
    • Dufour, R.; Daumar, P.; Mounetou, E.; Aubel, C.; Kwiatkowski, F.; Abrial, C.; Vatoux, C.; Penault-Llorca, F.; Bamdad, M. BCRP and P-gp relay overexpression in triple negative basal-like breast cancer cell line: a prospective role in resistance to Olaparib Sci. Rep. 2015, 5, 12670 10.1038/srep12670
    • (2015) Sci. Rep. , vol.5 , pp. 12670
    • Dufour, R.1    Daumar, P.2    Mounetou, E.3    Aubel, C.4    Kwiatkowski, F.5    Abrial, C.6    Vatoux, C.7    Penault-Llorca, F.8    Bamdad, M.9
  • 141
    • 0032539957 scopus 로고    scopus 로고
    • + binding to poly (ADP-ribose) polymerase as derived from crystal structures and homology modeling
    • + binding to poly (ADP-ribose) polymerase as derived from crystal structures and homology modeling Biochemistry 1998, 37, 3893-3900 10.1021/bi972383s
    • (1998) Biochemistry , vol.37 , pp. 3893-3900
    • Ruf, A.1    De Murcia, G.2    Schulz, G.E.3
  • 142
    • 0026601666 scopus 로고
    • Specific inhibitors of poly (ADP-ribose) synthetase and mono (ADP-ribosyl) transferase
    • Banasik, M.; Komura, H.; Shimoyama, M.; Ueda, K. Specific inhibitors of poly (ADP-ribose) synthetase and mono (ADP-ribosyl) transferase J. Biol. Chem. 1992, 267, 1569-1575
    • (1992) J. Biol. Chem. , vol.267 , pp. 1569-1575
    • Banasik, M.1    Komura, H.2    Shimoyama, M.3    Ueda, K.4
  • 143
    • 84959464644 scopus 로고    scopus 로고
    • 5-Aminoisoquinolin-1-one (5-AIQ), a water-soluble inhibitor of the poly(ADP-ribose)polymerases (PARPs)
    • Threadgill, M. D. 5-Aminoisoquinolin-1-one (5-AIQ), a water-soluble inhibitor of the poly(ADP-ribose)polymerases (PARPs) Curr. Med. Chem. 2015, 22, 3807-3829 10.2174/0929867322666151002110602
    • (2015) Curr. Med. Chem. , vol.22 , pp. 3807-3829
    • Threadgill, M.D.1
  • 147
    • 74049143159 scopus 로고    scopus 로고
    • Development of substituted 6-[4-fluoro-3- (piperazin-1-ylcarbonyl) benzyl]-4,5-dimethylpyridazin-3(2H)-ones as potent poly(ADP-ribose)polymerase-1 (PARP-1) inhibitors active in BRCA deficient cells
    • Ferrigno, F.; Branca, D.; Kinzel, O.; Lillini, S.; Bufi, L. L.; Monteagudo, E.; Muraglia, E.; Rowley, M.; Schultz-Fademrecht, C.; Toniatti, C.; Torrisi, C.; Jones, P. Development of substituted 6-[4-fluoro-3- (piperazin-1-ylcarbonyl) benzyl]-4,5-dimethylpyridazin-3(2H)-ones as potent poly(ADP-ribose)polymerase-1 (PARP-1) inhibitors active in BRCA deficient cells Bioorg. Med. Chem. Lett. 2010, 20, 1100-1105 10.1016/j.bmcl.2009.11.087
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 1100-1105
    • Ferrigno, F.1    Branca, D.2    Kinzel, O.3    Lillini, S.4    Bufi, L.L.5    Monteagudo, E.6    Muraglia, E.7    Rowley, M.8    Schultz-Fademrecht, C.9    Toniatti, C.10    Torrisi, C.11    Jones, P.12
  • 149
    • 84905924721 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of substituted 4-(thiophen-2-ylmethyl)-2H-phthalazin-1- ones as potent PARP-1 inhibitors
    • Wang, L. X.; Zhou, X. B.; Xiao, M. L.; Jiang, N.; Liu, F.; Zhou, W. X.; Wang, X. K.; Zheng, Z. B.; Li, S. Synthesis and biological evaluation of substituted 4-(thiophen-2-ylmethyl)-2H-phthalazin-1- ones as potent PARP-1 inhibitors Bioorg. Med. Chem. Lett. 2014, 24, 3739-3743 10.1016/j.bmcl.2014.07.001
    • (2014) Bioorg. Med. Chem. Lett. , vol.24 , pp. 3739-3743
    • Wang, L.X.1    Zhou, X.B.2    Xiao, M.L.3    Jiang, N.4    Liu, F.5    Zhou, W.X.6    Wang, X.K.7    Zheng, Z.B.8    Li, S.9
  • 150
    • 33947379595 scopus 로고    scopus 로고
    • PARP inhibitors enhance the effect of cisplatin against tumors and ameliorate cisplatin-induced neuropathy
    • Lapidus, R. G.; Xu, W.; Spicer, E.; Hoover, R.; Zhang, J. PARP inhibitors enhance the effect of cisplatin against tumors and ameliorate cisplatin-induced neuropathy Cancer Res. 2006, 66, 2141
    • (2006) Cancer Res. , vol.66 , pp. 2141
    • Lapidus, R.G.1    Xu, W.2    Spicer, E.3    Hoover, R.4    Zhang, J.5
  • 151
    • 85020159370 scopus 로고    scopus 로고
    • Phase i study of the safety, pharmacokinetics (PK), and pharmacodynamics (PD) of the poly (ADP-ribose) polymerase (PARP) inhibitor E7016 in combination with Temozolomide (TMZ) in patients with advanced solid tumors
    • Mita, A.; Mita, M.; Sarantopoulos, J.; Martin, J. C.; Kueber, J. D.; McGonigle, S.; Matijevic, M.; Mistry, B.; Ferrada, J. L.; Sachdev, P.; Stephenson, J. J., Jr Phase I study of the safety, pharmacokinetics (PK), and pharmacodynamics (PD) of the poly (ADP-ribose) polymerase (PARP) inhibitor E7016 in combination with Temozolomide (TMZ) in patients with advanced solid tumors Mol. Cancer Ther. 2011, 10 (11 suppl) B185 10.1158/1535-7163.TARG-11-B185
    • (2011) Mol. Cancer Ther. , vol.10 , Issue.11 , pp. B185
    • Mita, A.1    Mita, M.2    Sarantopoulos, J.3    Martin, J.C.4    Kueber, J.D.5    McGonigle, S.6    Matijevic, M.7    Mistry, B.8    Ferrada, J.L.9    Sachdev, P.10    Stephenson, J.J.11
  • 152
    • 84937759395 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of pyridazino [3, 4, 5-de]quinazolin-3(2H)-one as a new class of PARP-1 inhibitors
    • Wang, J.; Tan, H.; Sun, Q.; Ge, Z.; Wang, X.; Wang, Y.; Li, R. Design, synthesis and biological evaluation of pyridazino [3, 4, 5-de]quinazolin-3(2H)-one as a new class of PARP-1 inhibitors Bioorg. Med. Chem. Lett. 2015, 25, 2340-2344 10.1016/j.bmcl.2015.04.013
    • (2015) Bioorg. Med. Chem. Lett. , vol.25 , pp. 2340-2344
    • Wang, J.1    Tan, H.2    Sun, Q.3    Ge, Z.4    Wang, X.5    Wang, Y.6    Li, R.7
  • 153
    • 84907030375 scopus 로고    scopus 로고
    • 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, A. S.; Yip, B. K.; Wang, B.; Shen, Y.; Fitzpatrick, P. A. Structural basis for the inhibition of poly (ADP-ribose) polymerases 1 and 2 by BMN 673, a potent inhibitor derived from dihydropyridophthalazinone Acta Crystallogr., Sect. F: Struct. Biol. Commun. 2014, 70, 1143-1149 10.1107/S2053230X14015088
    • (2014) Acta Crystallogr., Sect. 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
  • 154
    • 84975490848 scopus 로고    scopus 로고
    • Abstract B64: Structure and preclinical characterization of BMN 673, a potent and orally active PARP inhibitor as an anticancer agent
    • Shen, Y.; Feng, Y.; Wang, B.; Myers, P.; Chu, D.; Post, L. E. Abstract B64: Structure and preclinical characterization of BMN 673, a potent and orally active PARP inhibitor as an anticancer agent Mol. Cancer Ther. 2011, 10 (11 suppl) B64 10.1158/1535-7163.TARG-11-B64
    • (2011) Mol. Cancer Ther. , vol.10 , Issue.11 , pp. B64
    • Shen, Y.1    Feng, Y.2    Wang, B.3    Myers, P.4    Chu, D.5    Post, L.E.6
  • 157
    • 77949654750 scopus 로고    scopus 로고
    • Synthesis and evaluation of tricyclic derivatives containing a non-aromatic amide as inhibitors of poly (ADP-ribose) polymerase-1 (PARP-1)
    • Park, C. H.; Chun, K.; Joe, B. Y.; Park, J. S.; Kim, Y. C.; Choi, J. S.; Ryu, D. K.; Koh, S. H.; Cho, G. W.; Kim, S. H.; Kim, M. H. Synthesis and evaluation of tricyclic derivatives containing a non-aromatic amide as inhibitors of poly (ADP-ribose) polymerase-1 (PARP-1) Bioorg. Med. Chem. Lett. 2010, 20, 2250-2253 10.1016/j.bmcl.2010.02.014
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 2250-2253
    • Park, C.H.1    Chun, K.2    Joe, B.Y.3    Park, J.S.4    Kim, Y.C.5    Choi, J.S.6    Ryu, D.K.7    Koh, S.H.8    Cho, G.W.9    Kim, S.H.10    Kim, M.H.11
  • 159
    • 84900816000 scopus 로고    scopus 로고
    • Synthesis of isoquinolinone-based tricycles as novel poly (ADP-ribose) polymerase-1 (PARP-1) inhibitors
    • Chen, J.; Peng, H.; He, J.; Huan, X.; Miao, Z.; Yang, C. Synthesis of isoquinolinone-based tricycles as novel poly (ADP-ribose) polymerase-1 (PARP-1) inhibitors Bioorg. Med. Chem. Lett. 2014, 24, 2669-2673 10.1016/j.bmcl.2014.04.061
    • (2014) Bioorg. Med. Chem. Lett. , vol.24 , pp. 2669-2673
    • Chen, J.1    Peng, H.2    He, J.3    Huan, X.4    Miao, Z.5    Yang, C.6
  • 160
    • 84876257495 scopus 로고    scopus 로고
    • 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, C. H.; Chen, T.; Song, Z.; He, J. X.; Huan, X. J.; Song, S. S.; Liu, Q.; Chen, Y.; Ding, J.; Xu, Y.; Miao, Z. H.; Zhang, A. 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. 2013, 56, 2885-2903 10.1021/jm301825t
    • (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    Xu, Y.11    Miao, Z.H.12    Zhang, A.13
  • 162
    • 84964308855 scopus 로고    scopus 로고
    • Discovery of 1-substituted benzyl-quinazoline-2, 4(1H,3H)-dione derivatives as novel poly (ADP-ribose) polymerase-1 inhibitors
    • Yao, H.; Ji, M.; Zhu, Z.; Zhou, J.; Cao, R.; Chen, X.; Xu, B. Discovery of 1-substituted benzyl-quinazoline-2, 4(1H,3H)-dione derivatives as novel poly (ADP-ribose) polymerase-1 inhibitors Bioorg. Med. Chem. 2015, 23, 681-693 10.1016/j.bmc.2014.12.071
    • (2015) Bioorg. Med. Chem. , vol.23 , pp. 681-693
    • Yao, H.1    Ji, M.2    Zhu, Z.3    Zhou, J.4    Cao, R.5    Chen, X.6    Xu, B.7
  • 163
    • 84959440170 scopus 로고    scopus 로고
    • Poly (ADP-ribose) polymerases inhibitor, Zj6413, as a potential therapeutic agent against breast cancer
    • Zhou, Q.; Ji, M.; Zhou, J.; Jin, J.; Xue, N.; Chen, J.; Xu, B.; Chen, X. Poly (ADP-ribose) polymerases inhibitor, Zj6413, as a potential therapeutic agent against breast cancer Biochem. Pharmacol. 2016, 107, 29-40 10.1016/j.bcp.2016.02.015
    • (2016) Biochem. Pharmacol. , vol.107 , pp. 29-40
    • Zhou, Q.1    Ji, M.2    Zhou, J.3    Jin, J.4    Xue, N.5    Chen, J.6    Xu, B.7    Chen, X.8
  • 164
    • 84875226877 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of novel imidazo[4, 5-c]pyridinecarboxamide derivatives as PARP-1 inhibitors
    • Zhu, Q.; Wang, X.; Chu, Z.; He, G.; Dong, G.; Xu, Y. Design, synthesis and biological evaluation of novel imidazo[4, 5-c]pyridinecarboxamide derivatives as PARP-1 inhibitors Bioorg. Med. Chem. Lett. 2013, 23, 1993-1996 10.1016/j.bmcl.2013.02.032
    • (2013) Bioorg. Med. Chem. Lett. , vol.23 , pp. 1993-1996
    • Zhu, Q.1    Wang, X.2    Chu, Z.3    He, G.4    Dong, G.5    Xu, Y.6
  • 165
    • 84904325637 scopus 로고    scopus 로고
    • 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, M. R.; Bhatt, A.; Steffen, J. D.; Chergui, A.; Murai, J.; Pommier, Y.; Pascal, J. M.; Trombetta, L. D.; Fronczek, F. R.; Talele, T. T. 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. 2014, 57, 5579-5601 10.1021/jm5002502
    • (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
  • 168
    • 57349119185 scopus 로고    scopus 로고
    • Imidazoquinolinone, imidazopyridine, and isoquinolindione derivatives as novel and potent inhibitors of the poly (ADP-ribose) polymerase (PARP): A comparison with standard PARP inhibitors
    • Eltze, T.; Boer, R.; Wagner, T.; Weinbrenner, S.; McDonald, M. C.; Thiemermann, C.; Bürkle, A.; Klein, T. Imidazoquinolinone, imidazopyridine, and isoquinolindione derivatives as novel and potent inhibitors of the poly (ADP-ribose) polymerase (PARP): a comparison with standard PARP inhibitors Mol. Pharm. 2008, 74, 1587-1598 10.1124/mol.108.048751
    • (2008) Mol. Pharm. , vol.74 , pp. 1587-1598
    • Eltze, T.1    Boer, R.2    Wagner, T.3    Weinbrenner, S.4    McDonald, M.C.5    Thiemermann, C.6    Bürkle, A.7    Klein, T.8
  • 174
    • 80054765289 scopus 로고    scopus 로고
    • Phenotypic characterization of Parp-1 and Parp-2 deficient mice and cells
    • Boehler, C.; Gauthier, L.; Yelamos, J.; Noll, A.; Schreiber, V.; Dantzer, F. Phenotypic characterization of Parp-1 and Parp-2 deficient mice and cells Methods Mol. Biol. 2011, 780, 313-336 10.1007/978-1-61779-270-0-19
    • (2011) Methods Mol. Biol. , vol.780 , pp. 313-336
    • Boehler, C.1    Gauthier, L.2    Yelamos, J.3    Noll, A.4    Schreiber, V.5    Dantzer, F.6
  • 176
    • 77956676464 scopus 로고    scopus 로고
    • 'Contextual' synthetic lethality and/or loss of heterozygosity: Tumor hypoxia and modification of DNA repair
    • Chan, N.; Bristow, R. G. ″Contextual″ synthetic lethality and/or loss of heterozygosity: tumor hypoxia and modification of DNA repair Clin. Cancer Res. 2010, 16, 4553-4560 10.1158/1078-0432.CCR-10-0527
    • (2010) Clin. Cancer Res. , vol.16 , pp. 4553-4560
    • Chan, N.1    Bristow, R.G.2
  • 178
    • 76649094290 scopus 로고    scopus 로고
    • Inhibition of poly(ADP-ribose) polymerase down-regulates BRCA1 and RAD51 in a pathway mediated by E2F4 and p130
    • Hegan, D. C.; Lu, Y.; Stachelek, G. C.; Crosby, M. E.; Bindra, R. S.; Glazer, P. M. Inhibition of poly(ADP-ribose) polymerase down-regulates BRCA1 and RAD51 in a pathway mediated by E2F4 and p130 Proc. Natl. Acad. Sci. U. S. A. 2010, 107, 2201-2206 10.1073/pnas.0904783107
    • (2010) Proc. Natl. Acad. Sci. U. S. A. , vol.107 , pp. 2201-2206
    • Hegan, D.C.1    Lu, Y.2    Stachelek, G.C.3    Crosby, M.E.4    Bindra, R.S.5    Glazer, P.M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.