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Volumn 77, Issue 9, 2017, Pages 2476-2487

Targeted degradation of BET proteins in triple-negative breast cancer

Author keywords

[No Author keywords available]

Indexed keywords

BETD 246; BETD 260; BETI 211; BROMODOMAIN AND EXTRA TERMINAL PROTEIN; BROMODOMAIN INHIBITOR; PROTEIN; UNCLASSIFIED DRUG; ANTINEOPLASTIC AGENT; CELL SURFACE RECEPTOR; DNER PROTEIN, HUMAN; MCL1 PROTEIN, HUMAN; NERVE PROTEIN; PROTEIN MCL 1;

EID: 85019050301     PISSN: 00085472     EISSN: 15387445     Source Type: Journal    
DOI: 10.1158/0008-5472.CAN-16-2622     Document Type: Article
Times cited : (159)

References (50)
  • 1
    • 80054984945 scopus 로고    scopus 로고
    • Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia
    • Dawson MA, Prinjha RK, Dittmann A, Giotopoulos G, Bantscheff M, Chan WI, et al. Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia. Nature 2011;478:529-33.
    • (2011) Nature , vol.478 , pp. 529-533
    • Dawson, M.A.1    Prinjha, R.K.2    Dittmann, A.3    Giotopoulos, G.4    Bantscheff, M.5    Chan, W.I.6
  • 2
    • 84959145415 scopus 로고    scopus 로고
    • Phase I population pharmacokinetic assessment of the oral bromodomain inhibitor OTX015 in patients with haematologic malignancies
    • Odore E, Lokiec F, Cvitkovic E, Bekradda M, Herait P, Bourdel F, et al. Phase I population pharmacokinetic assessment of the oral bromodomain inhibitor OTX015 in patients with haematologic malignancies. Clin Pharmacokinet 2016;55:397-405.
    • (2016) Clin Pharmacokinet , vol.55 , pp. 397-405
    • Odore, E.1    Lokiec, F.2    Cvitkovic, E.3    Bekradda, M.4    Herait, P.5    Bourdel, F.6
  • 3
    • 84962523963 scopus 로고    scopus 로고
    • Bromodomain inhibitor OTX015 in patients with acute leukaemia: A doseescalation, phase 1 study
    • Berthon C, Raffoux E, Thomas X, Vey N, Gomez-Roca C, Yee K, et al. Bromodomain inhibitor OTX015 in patients with acute leukaemia: a doseescalation, phase 1 study. Lancet Haematol 2016;3:e186-e95.
    • (2016) Lancet Haematol , vol.3 , pp. e186-e195
    • Berthon, C.1    Raffoux, E.2    Thomas, X.3    Vey, N.4    Gomez-Roca, C.5    Yee, K.6
  • 5
    • 84964727676 scopus 로고    scopus 로고
    • Clinical response of carcinomas harboring the BRD4-NUT oncoprotein to the targeted bromodomain inhibitor OTX015/MK-8628
    • Stathis A, Zucca E, Bekradda M, Gomez-Roca C, Delord J-P, de La Motte Rouge T, et al. Clinical response of carcinomas harboring the BRD4-NUT oncoprotein to the targeted bromodomain inhibitor OTX015/MK-8628. Cancer Discov 2016;6:492-500.
    • (2016) Cancer Discov , vol.6 , pp. 492-500
    • Stathis, A.1    Zucca, E.2    Bekradda, M.3    Gomez-Roca, C.4    Delord, J.-P.5    De La Motte Rouge, T.6
  • 6
    • 84962488380 scopus 로고    scopus 로고
    • Bromodomain inhibitor OTX015 in patients with lymphoma or multiple myeloma: A dose-escalation, open-label, pharmacokinetic, phase 1 study
    • Amorim S, Stathis A, Gleeson M, Iyengar S, Magarotto V, Leleu X, et al. Bromodomain inhibitor OTX015 in patients with lymphoma or multiple myeloma: a dose-escalation, open-label, pharmacokinetic, phase 1 study. Lancet Haematol 2016;3:e196-e204.
    • (2016) Lancet Haematol , vol.3 , pp. e196-e204
    • Amorim, S.1    Stathis, A.2    Gleeson, M.3    Iyengar, S.4    Magarotto, V.5    Leleu, X.6
  • 7
    • 84897024898 scopus 로고    scopus 로고
    • Potent antimyeloma activity of the novel bromodomain inhibitors IBET151 and I-BET762
    • Chaidos A, Caputo V, Gouvedenou K, Liu B, Marigo I, Chaudhry MS, et al. Potent antimyeloma activity of the novel bromodomain inhibitors IBET151 and I-BET762. Blood 2014;123:697-705.
    • (2014) Blood , vol.123 , pp. 697-705
    • Chaidos, A.1    Caputo, V.2    Gouvedenou, K.3    Liu, B.4    Marigo, I.5    Chaudhry, M.S.6
  • 8
    • 84955472185 scopus 로고    scopus 로고
    • Response and resistance to BET bromodomain inhibitors in triple-negative breast cancer
    • Shu S, Lin CY, He HH, Witwicki RM, Tabassum DP, Roberts JM, et al. Response and resistance to BET bromodomain inhibitors in triple-negative breast cancer. Nature 2016;529:413-7.
    • (2016) Nature , vol.529 , pp. 413-417
    • Shu, S.1    Lin, C.Y.2    He, H.H.3    Witwicki, R.M.4    Tabassum, D.P.5    Roberts, J.M.6
  • 9
    • 84925384930 scopus 로고    scopus 로고
    • Inhibition of BET proteins impairs estrogen-mediated growth and transcription in breast cancers by pausing RNA polymerase advancement
    • Sengupta S, Biarnes MC, Clarke R, Jordan VC. Inhibition of BET proteins impairs estrogen-mediated growth and transcription in breast cancers by pausing RNA polymerase advancement. Breast Cancer Res Treat 2015; 150:265-78.
    • (2015) Breast Cancer Res Treat , vol.150 , pp. 265-278
    • Sengupta, S.1    Biarnes, M.C.2    Clarke, R.3    Jordan, V.C.4
  • 10
    • 84904811353 scopus 로고    scopus 로고
    • Bromodomain protein BRD4 is required for estrogen receptor-dependent enhancer activation and gene transcription
    • Nagarajan S, Hossan T, Alawi M, Najafova Z, Indenbirken D, Bedi U, et al. Bromodomain protein BRD4 is required for estrogen receptor-dependent enhancer activation and gene transcription. Cell Rep 2014;8:460-9.
    • (2014) Cell Rep , vol.8 , pp. 460-469
    • Nagarajan, S.1    Hossan, T.2    Alawi, M.3    Najafova, Z.4    Indenbirken, D.5    Bedi, U.6
  • 11
    • 84954290430 scopus 로고    scopus 로고
    • Functional genomic landscape of human breast cancer drivers, vulnerabilities, and resistance
    • Marcotte R, Sayad A, Brown KR, Sanchez-Garcia F, Reimand J, Haider M, et al. Functional genomic landscape of human breast cancer drivers, vulnerabilities, and resistance. Cell 2016;164:293-309.
    • (2016) Cell , vol.164 , pp. 293-309
    • Marcotte, R.1    Sayad, A.2    Brown, K.R.3    Sanchez-Garcia, F.4    Reimand, J.5    Haider, M.6
  • 12
    • 0035902475 scopus 로고    scopus 로고
    • Protacs: Chimeric molecules that target proteins to the Skp1-Cullin-F box complex for ubiquitination and degradation
    • Sakamoto KM, Kim KB, Kumagai A, Mercurio F, Crews CM, Deshaies RJ. Protacs: chimeric molecules that target proteins to the Skp1-Cullin-F box complex for ubiquitination and degradation. Proc Natl Acad Sci U S A 2001;98:8554-9.
    • (2001) Proc Natl Acad Sci U S A , vol.98 , pp. 8554-8559
    • Sakamoto, K.M.1    Kim, K.B.2    Kumagai, A.3    Mercurio, F.4    Crews, C.M.5    Deshaies, R.J.6
  • 13
    • 84961285814 scopus 로고    scopus 로고
    • Small-molecule PROTACS: New approaches to protein degradation
    • Toure M, Crews CM. Small-molecule PROTACS: new approaches to protein degradation. Angew Chem Int Ed Engl 2016;55:1966-73.
    • (2016) Angew Chem Int Ed Engl , vol.55 , pp. 1966-1973
    • Toure, M.1    Crews, C.M.2
  • 14
    • 84932634729 scopus 로고    scopus 로고
    • Phthalimide conjugation as a strategy for in vivo target protein degradation
    • DRUG DEVELOPMENT
    • Winter GE, Buckley DL, Paulk J, Roberts JM, Souza A, Dhe-Paganon S, et al. DRUG DEVELOPMENT. Phthalimide conjugation as a strategy for in vivo target protein degradation. Science 2015;348:1376-81.
    • (2015) Science , vol.348 , pp. 1376-1381
    • Winter, G.E.1    Buckley, D.L.2    Paulk, J.3    Roberts, J.M.4    Souza, A.5    Dhe-Paganon, S.6
  • 15
    • 84931560527 scopus 로고    scopus 로고
    • Hijacking the E3 ubiquitin ligase cereblon to efficiently target BRD4
    • Lu J, Qian Y, Altieri M, Dong H, Wang J, Raina K, et al. Hijacking the E3 ubiquitin ligase cereblon to efficiently target BRD4. Chem Biol 2015; 22:755-63.
    • (2015) Chem Biol , vol.22 , pp. 755-763
    • Lu, J.1    Qian, Y.2    Altieri, M.3    Dong, H.4    Wang, J.5    Raina, K.6
  • 16
    • 84976614642 scopus 로고    scopus 로고
    • PROTACinduced BET protein degradation as a therapy for castration-resistant prostate cancer
    • Raina K, Lu J, Qian Y, Altieri M, Gordon D, Rossi AM, et al. PROTACinduced BET protein degradation as a therapy for castration-resistant prostate cancer. Proc Natl Acad Sci U S A 2016;113:7124-9.
    • (2016) Proc Natl Acad Sci U S A , vol.113 , pp. 7124-7129
    • Raina, K.1    Lu, J.2    Qian, Y.3    Altieri, M.4    Gordon, D.5    Rossi, A.M.6
  • 17
    • 0027510686 scopus 로고
    • Differential isolation of normal luminal mammary epithelial cells and breast cancer cells from primary and metastatic sites using selective media
    • Ethier SP, Mahacek ML, Gullick WJ, Frank TS, Weber BL. Differential isolation of normal luminal mammary epithelial cells and breast cancer cells from primary and metastatic sites using selective media. Cancer Res 1993;53:627-35.
    • (1993) Cancer Res , vol.53 , pp. 627-635
    • Ethier, S.P.1    Mahacek, M.L.2    Gullick, W.J.3    Frank, T.S.4    Weber, B.L.5
  • 18
    • 84902477584 scopus 로고    scopus 로고
    • BM-1197: A novel and specific Bcl-2/Bcl-xL inhibitor inducing complete and longlasting tumor regression in vivo
    • Bai L, Chen J, McEachern D, Liu L, Zhou H, Aguilar A, et al. BM-1197: a novel and specific Bcl-2/Bcl-xL inhibitor inducing complete and longlasting tumor regression in vivo. PLoS ONE 2014;9:e99404.
    • (2014) PLoS ONE , vol.9 , pp. e99404
    • Bai, L.1    Chen, J.2    McEachern, D.3    Liu, L.4    Zhou, H.5    Aguilar, A.6
  • 19
    • 84941963589 scopus 로고    scopus 로고
    • Elucidation of acquired resistance to Bcl-2 andMDM2inhibitors in acute leukemia in vitro and in vivo
    • Hoffman-Luca CG, Ziazadeh D, McEachern D, Zhao Y, Sun W, Debussche L, et al. Elucidation of acquired resistance to Bcl-2 andMDM2inhibitors in acute leukemia in vitro and in vivo. Clin Cancer Res 2015;21:2558-68.
    • (2015) Clin Cancer Res , vol.21 , pp. 2558-2568
    • Hoffman-Luca, C.G.1    Ziazadeh, D.2    McEachern, D.3    Zhao, Y.4    Sun, W.5    Debussche, L.6
  • 20
    • 84933044675 scopus 로고    scopus 로고
    • Structure-based design of gamma-carboline analogues as potent and specific BET bromodomain inhibitors
    • Ran X, Zhao Y, Liu L, Bai L, Yang CY, Zhou B, et al. Structure-based design of gamma-carboline analogues as potent and specific BET bromodomain inhibitors. J Med Chem 2015;58:4927-39.
    • (2015) J Med Chem , vol.58 , pp. 4927-4939
    • Ran, X.1    Zhao, Y.2    Liu, L.3    Bai, L.4    Yang, C.Y.5    Zhou, B.6
  • 21
    • 34447116376 scopus 로고    scopus 로고
    • Antitumor activity of PR-171, a novel irreversible inhibitor of the proteasome
    • Demo SD, Kirk CJ, Aujay MA, Buchholz TJ, Dajee M, Ho MN, et al. Antitumor activity of PR-171, a novel irreversible inhibitor of the proteasome. Cancer Res 2007;67:6383-91.
    • (2007) Cancer Res , vol.67 , pp. 6383-6391
    • Demo, S.D.1    Kirk, C.J.2    Aujay, M.A.3    Buchholz, T.J.4    Dajee, M.5    Ho, M.N.6
  • 23
    • 2442623052 scopus 로고    scopus 로고
    • Cullin-based ubiquitin ligase and its control by NEDD8-conjugating system
    • Chiba T, Tanaka K. Cullin-based ubiquitin ligase and its control by NEDD8-conjugating system. Curr Protein Pept Sci 2004;5:177-84.
    • (2004) Curr Protein Pept Sci , vol.5 , pp. 177-184
    • Chiba, T.1    Tanaka, K.2
  • 24
    • 80055000824 scopus 로고    scopus 로고
    • RNAi screen identifies Brd4 as a therapeutic target in acute myeloid leukaemia
    • Zuber J, Shi J, Wang E, Rappaport AR, Herrmann H, Sison EA, et al. RNAi screen identifies Brd4 as a therapeutic target in acute myeloid leukaemia. Nature 2011;478:524-8.
    • (2011) Nature , vol.478 , pp. 524-528
    • Zuber, J.1    Shi, J.2    Wang, E.3    Rappaport, A.R.4    Herrmann, H.5    Sison, E.A.6
  • 25
    • 80052955256 scopus 로고    scopus 로고
    • BET bromodomain inhibition as a therapeutic strategy to target c-Myc
    • Delmore JE, Issa GC, Lemieux ME, Rahl PB, Shi J, Jacobs HM, et al. BET bromodomain inhibition as a therapeutic strategy to target c-Myc. Cell 2011;146:904-17.
    • (2011) Cell , vol.146 , pp. 904-917
    • Delmore, J.E.1    Issa, G.C.2    Lemieux, M.E.3    Rahl, P.B.4    Shi, J.5    Jacobs, H.M.6
  • 27
    • 84877097843 scopus 로고    scopus 로고
    • Inhibition of BET bromodomain targets genetically diverse glioblastoma
    • Cheng Z, Gong Y, Ma Y, Lu K, Lu X, Pierce LA, et al. Inhibition of BET bromodomain targets genetically diverse glioblastoma. Clin Cancer Res 2013;19:1748-59.
    • (2013) Clin Cancer Res , vol.19 , pp. 1748-1759
    • Cheng, Z.1    Gong, Y.2    Ma, Y.3    Lu, K.4    Lu, X.5    Pierce, L.A.6
  • 28
    • 84966586078 scopus 로고    scopus 로고
    • Targeting the epigenetic readers in Ewing Sarcoma inhibits the oncogenic transcription factor EWS/Fli1
    • Jacques C, Lamoureux F, Baud'huin M, Calleja LR, Quillard T, Amiaud J, et al. Targeting the epigenetic readers in Ewing Sarcoma inhibits the oncogenic transcription factor EWS/Fli1. Oncotarget 2016;7: 24125-40.
    • (2016) Oncotarget , vol.7 , pp. 24125-24140
    • Jacques, C.1    Lamoureux, F.2    Baud'Huin, M.3    Calleja, L.R.4    Quillard, T.5    Amiaud, J.6
  • 29
    • 84947492264 scopus 로고    scopus 로고
    • Myeloid cell leukemia-1 is an important apoptotic survival factor in triple-negative breast cancer
    • Goodwin CM, Rossanese OW, Olejniczak ET, Fesik SW. Myeloid cell leukemia-1 is an important apoptotic survival factor in triple-negative breast cancer. Cell Death Differ 2015;22:2098-106.
    • (2015) Cell Death Differ , vol.22 , pp. 2098-2106
    • Goodwin, C.M.1    Rossanese, O.W.2    Olejniczak, E.T.3    Fesik, S.W.4
  • 30
    • 84942103252 scopus 로고    scopus 로고
    • MCL-1 is a key determinant of breast cancer cell survival: Validation of MCL-1 dependency utilizing a highly selective small molecule inhibitor
    • Xiao Y, Nimmer P, SheppardGS, Bruncko M, Hessler P, Lu X, et al.MCL-1 is a key determinant of breast cancer cell survival: validation of MCL-1 dependency utilizing a highly selective small molecule inhibitor. Mol Cancer Ther 2015;14:1837-47.
    • (2015) Mol Cancer Ther , vol.14 , pp. 1837-1847
    • Xiao, Y.1    Nimmer, P.2    Sheppard, G.S.3    Bruncko, M.4    Hessler, P.5    Lu, X.6
  • 31
    • 84881499406 scopus 로고    scopus 로고
    • A genome-wide siRNA screen identifies proteasome addiction as a vulnerability of basal-like triple-negative breast cancer cells
    • Petrocca F, Altschuler G, Tan SM, Mendillo ML, Yan H, Jerry DJ, et al. A genome-wide siRNA screen identifies proteasome addiction as a vulnerability of basal-like triple-negative breast cancer cells. Cancer Cell 2013;24:182-96.
    • (2013) Cancer Cell , vol.24 , pp. 182-196
    • Petrocca, F.1    Altschuler, G.2    Tan, S.M.3    Mendillo, M.L.4    Yan, H.5    Jerry, D.J.6
  • 33
  • 34
    • 84873540049 scopus 로고    scopus 로고
    • ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets
    • Souers AJ, Leverson JD, Boghaert ER, Ackler SL, Catron ND, Chen J, et al. ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets. Nat Med 2013;19:202-8.
    • (2013) Nat Med , vol.19 , pp. 202-208
    • Souers, A.J.1    Leverson, J.D.2    Boghaert, E.R.3    Ackler, S.L.4    Catron, N.D.5    Chen, J.6
  • 35
    • 0019750732 scopus 로고
    • Criteria for analyzing interactions between biologically active agents
    • Berenbaum MC. Criteria for analyzing interactions between biologically active agents. Adv Cancer Res 1981;35:269-335.
    • (1981) Adv Cancer Res , vol.35 , pp. 269-335
    • Berenbaum, M.C.1
  • 36
    • 84884559238 scopus 로고    scopus 로고
    • Endocrine-therapyresistant ESR1 variants revealed by genomic characterization of breastcancer-derived xenografts
    • Li S, Shen D, Shao J, Crowder R, Liu W, Prat A, et al. Endocrine-therapyresistant ESR1 variants revealed by genomic characterization of breastcancer-derived xenografts. Cell Rep 2013;4:1116-30.
    • (2013) Cell Rep , vol.4 , pp. 1116-1130
    • Li, S.1    Shen, D.2    Shao, J.3    Crowder, R.4    Liu, W.5    Prat, A.6
  • 37
    • 84862738480 scopus 로고    scopus 로고
    • BET domain co-regulators in obesity, inflammation and cancer
    • Belkina AC, Denis GV. BET domain co-regulators in obesity, inflammation and cancer. Nat Rev Cancer 2012;12:465-77.
    • (2012) Nat Rev Cancer , vol.12 , pp. 465-477
    • Belkina, A.C.1    Denis, G.V.2
  • 38
    • 84901821841 scopus 로고    scopus 로고
    • The mechanisms behind the therapeutic activity of BET bromodomain inhibition
    • Shi J, Vakoc CR. The mechanisms behind the therapeutic activity of BET bromodomain inhibition. Mol Cell 2014;54:728-36.
    • (2014) Mol Cell , vol.54 , pp. 728-736
    • Shi, J.1    Vakoc, C.R.2
  • 39
    • 84962683838 scopus 로고    scopus 로고
    • BET bromodomain inhibition releases the mediator complex from select cis-regulatory elements
    • Bhagwat AS, Roe JS, Mok BY, Hohmann AF, Shi J, Vakoc CR. BET bromodomain inhibition releases the mediator complex from select cis-regulatory elements. Cell Rep 2016;15:519-30.
    • (2016) Cell Rep , vol.15 , pp. 519-530
    • Bhagwat, A.S.1    Roe, J.S.2    Mok, B.Y.3    Hohmann, A.F.4    Shi, J.5    Vakoc, C.R.6
  • 40
    • 84953635251 scopus 로고    scopus 로고
    • NSD3-short is an adaptor protein that couples BRD4 to the CHD8 chromatin remodeler
    • Shen C, Ipsaro JJ, Shi J,Milazzo JP, Wang E, Roe JS, et al. NSD3-short is an adaptor protein that couples BRD4 to the CHD8 chromatin remodeler. Mol Cell 2015;60:847-59.
    • (2015) Mol Cell , vol.60 , pp. 847-859
    • Shen, C.1    Ipsaro, J.J.2    Shi, J.3    Milazzo, J.P.4    Wang, E.5    Roe, J.S.6
  • 41
    • 84937639611 scopus 로고    scopus 로고
    • BET bromodomain inhibition suppresses the function of hematopoietic transcription factors in acute myeloid leukemia
    • Roe JS, Mercan F, Rivera K, Pappin DJ, Vakoc CR. BET bromodomain inhibition suppresses the function of hematopoietic transcription factors in acute myeloid leukemia. Mol Cell 2015;58:1028-39.
    • (2015) Mol Cell , vol.58 , pp. 1028-1039
    • Roe, J.S.1    Mercan, F.2    Rivera, K.3    Pappin, D.J.4    Vakoc, C.R.5
  • 42
    • 84891953718 scopus 로고    scopus 로고
    • Discovery and characterization of super-enhancer-associated dependencies in diffuse large B cell lymphoma
    • Chapuy B, McKeown MR, Lin CY, Monti S, Roemer MG, Qi J, et al. Discovery and characterization of super-enhancer-associated dependencies in diffuse large B cell lymphoma. Cancer Cell 2013;24:777-90.
    • (2013) Cancer Cell , vol.24 , pp. 777-790
    • Chapuy, B.1    McKeown, M.R.2    Lin, C.Y.3    Monti, S.4    Roemer, M.G.5    Qi, J.6
  • 43
    • 84961992304 scopus 로고    scopus 로고
    • Preclinical anticancer efficacy of BET bromodomain inhibitors is determined by the apoptotic response
    • Conery AR, Centore RC, Spillane KL, Follmer NE, Bommi-Reddy A, Hatton C, et al. Preclinical anticancer efficacy of BET bromodomain inhibitors is determined by the apoptotic response. Cancer Res 2016;76:1313-9.
    • (2016) Cancer Res , vol.76 , pp. 1313-1319
    • Conery, A.R.1    Centore, R.C.2    Spillane, K.L.3    Follmer, N.E.4    Bommi-Reddy, A.5    Hatton, C.6
  • 44
    • 34250327394 scopus 로고    scopus 로고
    • Myeloid cell leukemia-1 inversely correlates with glycogen synthase kinase-3beta activity and associates with poor prognosis in human breast cancer
    • Ding Q, He X, Xia W, Hsu JM, Chen CT, Li LY, et al. Myeloid cell leukemia-1 inversely correlates with glycogen synthase kinase-3beta activity and associates with poor prognosis in human breast cancer. Cancer Res 2007;67:4564-71.
    • (2007) Cancer Res , vol.67 , pp. 4564-4571
    • Ding, Q.1    He, X.2    Xia, W.3    Hsu, J.M.4    Chen, C.T.5    Li, L.Y.6
  • 45
    • 84896689570 scopus 로고    scopus 로고
    • Molecular profiling of the residual disease of triple-negative breast cancers after neoadjuvant chemotherapy identifies actionable therapeutic targets
    • Balko JM, Giltnane JM, Wang K, Schwarz LJ, Young CD, Cook RS, et al. Molecular profiling of the residual disease of triple-negative breast cancers after neoadjuvant chemotherapy identifies actionable therapeutic targets. Cancer Discov 2014;4:232-45.
    • (2014) Cancer Discov , vol.4 , pp. 232-245
    • Balko, J.M.1    Giltnane, J.M.2    Wang, K.3    Schwarz, L.J.4    Young, C.D.5    Cook, R.S.6
  • 47
    • 33644973070 scopus 로고    scopus 로고
    • Prognostic value of pathologic complete response after primary chemotherapy in relation to hormone receptor status and other factors
    • Guarneri V, Broglio K, Kau SW, Cristofanilli M, Buzdar AU, Valero V, et al. Prognostic value of pathologic complete response after primary chemotherapy in relation to hormone receptor status and other factors. J Clin Oncol 2006;24:1037-44.
    • (2006) J Clin Oncol , vol.24 , pp. 1037-1044
    • Guarneri, V.1    Broglio, K.2    Kau, S.W.3    Cristofanilli, M.4    Buzdar, A.U.5    Valero, V.6
  • 48
    • 0033050164 scopus 로고    scopus 로고
    • Clinical course of breast cancer patients with complete pathologic primary tumor and axillary lymph node response to doxorubicin-based neoadjuvant chemotherapy
    • Kuerer HM, Newman LA, Smith TL, Ames FC, Hunt KK, Dhingra K, et al. Clinical course of breast cancer patients with complete pathologic primary tumor and axillary lymph node response to doxorubicin-based neoadjuvant chemotherapy. J Clin Oncol 1999;17: 460-9.
    • (1999) J Clin Oncol , vol.17 , pp. 460-469
    • Kuerer, H.M.1    Newman, L.A.2    Smith, T.L.3    Ames, F.C.4    Hunt, K.K.5    Dhingra, K.6
  • 49
    • 41649102048 scopus 로고    scopus 로고
    • Response to neoadjuvant therapy and long-term survival in patients with triplenegative breast cancer
    • Liedtke C, Mazouni C, Hess KR, Andre F, Tordai A, Mejia JA, et al. Response to neoadjuvant therapy and long-term survival in patients with triplenegative breast cancer. J Clin Oncol 2008;26:1275-81.
    • (2008) J Clin Oncol , vol.26 , pp. 1275-1281
    • Liedtke, C.1    Mazouni, C.2    Hess, K.R.3    Andre, F.4    Tordai, A.5    Mejia, J.A.6
  • 50
    • 79952271269 scopus 로고    scopus 로고
    • Sensitivity to antitubulin chemotherapeutics is regulated by MCL1 and FBW7
    • Wertz IE, Kusam S, Lam C, Okamoto T, Sandoval W, Anderson DJ, et al. Sensitivity to antitubulin chemotherapeutics is regulated by MCL1 and FBW7. Nature 2011;471:110-4.
    • (2011) Nature , vol.471 , pp. 110-114
    • Wertz, I.E.1    Kusam, S.2    Lam, C.3    Okamoto, T.4    Sandoval, W.5    Anderson, D.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.