Recent therapeutic trends and promising targets in triple negative breast cancer

被引:182
作者
Hwang, Soo-Yeon [1 ]
Park, Seojeong [1 ]
Kwon, Youngjoo [1 ]
机构
[1] Ewha Womans Univ, Coll Pharm, Grad Sch Pharmaceut Sci, Seoul 03760, South Korea
基金
新加坡国家研究基金会;
关键词
Metastatic triple negative breast cancer (mTNBC); Targeted therapy; Small molecules; Clinical trials; Experimental targets; Preclinical implication; ENDOTHELIAL GROWTH-FACTOR; TUMOR-INFILTRATING LYMPHOCYTES; TYROSINE KINASE INHIBITOR; ACTIVATED PROTEIN-KINASE; MOLECULE MDM2 INHIBITOR; AFRICAN-AMERICAN WOMEN; MULTICENTER PHASE-II; CELL LUNG-CANCER; FACTOR-RECEPTOR; ANDROGEN RECEPTOR;
D O I
10.1016/j.pharmthera.2019.02.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Breast cancer accounts for 25% of all types of cancer in women, and triple negative breast cancer (TNBC) comprises around 15 similar to 20% of breast cancers. Conventional chemotherapy and radiation are the primary systemic therapeutic strategies; no other FDA-approved targeted therapies are yet available as for TNBC TNBC is generally characterized by a poor prognosis and high rates of proliferation and metastases. Due to these aggressive features and lack of targeted therapies, numerous attempts have been made to discover viable molecular targets for TNBC Massive cohort studies, clinical trials, and in-depth analyses have revealed diverse molecular alterations in TNBC; however, controversy exists as to whether many of these changes are beneficial or detrimental in caner progression. Here we review the complicated tumorigenic processes and discuss critical findings and therapeutic trends in TNBC with a focus on promising therapeutic approaches, the clinical trials currently underway, and potent experimental compounds under preclinical and evaluation. (C) 2019 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:30 / 57
页数:28
相关论文
共 323 条
[1]  
Abdelgadir Elamin, 2017, J Clin Med Res, V9, P388, DOI 10.14740/jocmr2922e
[2]   The vascular endothelial growth factor family; proteins which guide the development of the vasculature [J].
Achen, MG ;
Stacker, SA .
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 1998, 79 (05) :255-265
[3]   Prognostic Value of Tumor-Infiltrating Lymphocytes in Triple-Negative Breast Cancers From Two Phase III Randomized Adjuvant Breast Cancer Trials: ECOG 2197 and ECOG 1199 [J].
Adams, Sylvia ;
Gray, Robert J. ;
Demaria, Sandra ;
Goldstein, Lori ;
Perez, Edith A. ;
Shulman, Lawrence N. ;
Martino, Silvana ;
Wang, Molin ;
Jones, Vicky E. ;
Saphner, Thomas J. ;
Wolff, Antonio C. ;
Wood, William C. ;
Davidson, Nancy E. ;
Sledge, George W. ;
Sparano, Joseph A. ;
Badve, Sunil S. .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (27) :2959-+
[4]   Hsp90 Inhibition Results in Glucocorticoid Receptor Degradation in Association with Increased Sensitivity to Paclitaxel in Triple-Negative Breast Cancer [J].
Agyeman, Abena S. ;
Jun, Wesley J. ;
Proia, David A. ;
Kim, Caroline R. ;
Skor, Maxwell N. ;
Kocherginsky, Masha ;
Conzen, Suzanne D. .
HORMONES & CANCER, 2016, 7 (02) :114-126
[5]   Targeting ataxia telangiectasia-mutated- and Rad3-related kinase (ATR) in PTEN-deficient breast cancers for personalized therapy [J].
Al-Subhi, Nouf ;
Ali, Reem ;
Abdel-Fatah, Tarek ;
Moseley, Paul M. ;
Chan, Stephen Y. T. ;
Green, Andrew R. ;
Ellis, Ian O. ;
Rakha, Emad A. ;
Madhusudan, Srinivasan .
BREAST CANCER RESEARCH AND TREATMENT, 2018, 169 (02) :277-286
[6]   Chk1 as a new therapeutic target in triple-negative breast cancer [J].
Albiges, Laurence ;
Goubar, Aicha ;
Scott, Veronique ;
Vicier, Cecile ;
Lefebvre, Celine ;
Alsafadi, Samar ;
Commo, Frederic ;
Saghatchian, Mahasti ;
Lazar, Vladimir ;
Dessen, Philippe ;
Delaloge, Suzette ;
Andre, Fabrice ;
Quidville, Virginie .
BREAST, 2014, 23 (03) :250-258
[7]   Conducting Molecular Epidemiological Research in the Age of HIPAA: A Multi-Institutional Case-Control Study of Breast Cancer in African-American and European-American Women [J].
Ambrosone, Christine B. ;
Ciupak, Gregory L. ;
Bandera, Elisa V. ;
Jandorf, Lina ;
Bovbjerg, Dana H. ;
Zirpoli, Gary ;
Pawlish, Karen ;
Godbold, James ;
Furberg, Helena ;
Fatone, Anne ;
Valdimarsdottir, Heiddis ;
Yao, Song ;
Li, Yulin ;
Hwang, Helena ;
Davis, Warren ;
Roberts, Michelle ;
Sucheston, Lara ;
Demissie, Kitaw ;
Amend, Kandace L. ;
Tartter, Paul ;
Reilly, James ;
Pace, Benjamin W. ;
Rohan, Thomas ;
Sparano, Joseph ;
Raptis, George ;
Castaldi, Maria ;
Estabrook, Alison ;
Feldman, Sheldon ;
Weltz, Christina ;
Kemeny, Margaret .
JOURNAL OF ONCOLOGY, 2009, 2009
[8]   Targeting FGFR with Dovitinib (TKI258): Preclinical and Clinical Data in Breast Cancer [J].
Andre, Fabrice ;
Bachelot, Thomas ;
Campone, Mario ;
Dalenc, Florence ;
Perez-Garcia, Jose M. ;
Hurvitz, Sara A. ;
Turner, Nicholas ;
Rugo, Hope ;
Smith, John W. ;
Deudon, Stephanie ;
Shi, Michael ;
Zhang, Yong ;
Kay, Andrea ;
Porta, Diana Graus ;
Yovine, Alejandro ;
Baselga, Jose .
CLINICAL CANCER RESEARCH, 2013, 19 (13) :3693-3702
[9]   Results of the Phase I Trial of RG7112, a Small-Molecule MDM2 Antagonist in Leukemia [J].
Andreeff, Michael ;
Kelly, Kevin R. ;
Yee, Karen ;
Assouline, Sarit ;
Strair, Roger ;
Popplewell, Leslie ;
Bowen, David ;
Martinelli, Giovanni ;
Drummond, Mark W. ;
Vyas, Paresh ;
Kirschbaum, Mark ;
Iyer, Swaminathan Padmanabhan ;
Ruvolo, Vivian ;
Gonzalez, Graciela M. Nogueras ;
Huang, Xuelin ;
Chen, Gong ;
Graves, Bradford ;
Blotner, Steven ;
Bridge, Peter ;
Jukofsky, Lori ;
Middleton, Steve ;
Reckner, Monica ;
Rueger, Ruediger ;
Zhi, Jianguo ;
Nichols, Gwen ;
Kojima, Kensuke .
CLINICAL CANCER RESEARCH, 2016, 22 (04) :868-876
[10]  
[Anonymous], J BREAST CANC RES AD