Triple-negative breast cancer: is there a treatment on the horizon?

被引:292
作者
Yao, Hui [1 ]
He, Guangchun [1 ]
Yan, Shichao [1 ]
Chen, Chao [1 ]
Song, Liujiang [2 ]
Rosol, Thomas J. [3 ]
Deng, Xiyun [1 ]
机构
[1] Hunan Normal Univ, Coll Med, Dept Pathol, Changsha, Hunan, Peoples R China
[2] Hunan Normal Univ, Coll Med, Dept Pediat, Changsha, Hunan, Peoples R China
[3] Ohio State Univ, Dept Vet Biosci, Columbus, OH 43210 USA
基金
中国国家自然科学基金;
关键词
breast cancer; triple-negative; therapeutics; PLATINUM-BASED CHEMOTHERAPY; BASAL-LIKE; STATIN USE; PHASE-II; POLY(ADP-RIBOSE) POLYMERASE; MOLECULAR CHARACTERIZATION; PRECLINICAL MODELS; PROSTATE-CANCER; CELL-LINES; SUBTYPES;
D O I
10.18632/oncotarget.12284
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triple-negative breast cancer (TNBC), which accounts for 15-20% of all breast cancers, does not express estrogen receptor (ER) or progesterone receptor (PR) and lacks human epidermal growth factor receptor 2 (HER2) overexpression or amplification. These tumors have a more aggressive phenotype and a poorer prognosis due to the high propensity for metastatic progression and absence of specific targeted treatments. Patients with TNBC do not benefit from hormonal or trastuzumab-based targeted therapies because of the loss of target receptors. Although these patients respond to chemotherapeutic agents such as taxanes and anthracyclines better than other subtypes of breast cancer, prognosis remains poor. A group of targeted therapies under investigation showed favorable results in TNBC, especially in cancers with BRCA mutation. The lipid-lowering statins (3-hydroxy-3-methyl-glutaryl coenzyme A reductase inhibitors), including lovastatin and simvastatin, have been shown to preferentially target TNBC compared with non-TNBC. These statins hold great promise for the management of TNBC. Only with the understanding of the molecular basis for the preference of statins for TNBC and more investigations in clinical trials can they be reformulated into a clinically approved drug against TNBC.
引用
收藏
页码:1913 / 1924
页数:12
相关论文
共 85 条
[1]   Statin Prescriptions and Breast Cancer Recurrence Risk: A Danish Nationwide Prospective Cohort Study [J].
Ahern, Thomas P. ;
Pedersen, Lars ;
Tarp, Maja ;
Cronin-Fenton, Deirdre P. ;
Garne, Jens Peter ;
Silliman, Rebecca A. ;
Sorensen, Henrik Toft ;
Lash, Timothy L. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2011, 103 (19) :1461-1468
[2]  
Anders C, 2008, ONCOLOGY, V22, P43
[3]  
Anders C, 2008, ONCOLOGY-NY, V22, P1233
[4]   Biology, Metastatic Patterns, and Treatment of Patients with Triple-Negative Breast Cancer [J].
Anders, Carey K. ;
Carey, Lisa A. .
CLINICAL BREAST CANCER, 2009, 9 :S73-S81
[5]  
[Anonymous], 2008, ONCOLOGY WILLISTON P
[6]   Novel treatment strategies in triple-negative breast cancer: specific role of poly(adenosine diphosphate-ribose) polymerase inhibition [J].
Audeh, M. William .
PHARMACOGENOMICS & PERSONALIZED MEDICINE, 2014, 7 :307-316
[7]   Basal-like breast carcinomas: clinical outcome and response to chemotherapy [J].
Banerjee, S. ;
Reis-Filho, J. S. ;
Ashley, S. ;
Steele, D. ;
Ashworth, A. ;
Lakhani, S. R. ;
Smith, I. E. .
JOURNAL OF CLINICAL PATHOLOGY, 2006, 59 (07) :729-735
[8]   Phase II Genomics Study of Ixabepilone as Neoadjuvant Treatment for Breast Cancer [J].
Baselga, Jose ;
Zambetti, Milvia ;
Llombart-Cussac, Antoni ;
Manikhas, Georgy ;
Kubista, Ernst ;
Steger, Guenther G. ;
Makhson, Anatoly ;
Tjulandin, Sergei ;
Ludwig, Heinz ;
Verrill, Mark ;
Ciruelos, Eva ;
Egyhazi, Suzanne ;
Xu, Li-An ;
Zerba, Kim E. ;
Lee, Hyerim ;
Clark, Edwin ;
Galbraith, Susan .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (04) :526-534
[9]   How basal are triple-negative breast cancers? [J].
Bertucci, Francois ;
Finetti, Pascal ;
Cervera, Nathalie ;
Esterni, Benjamin ;
Hermitte, Fabienne ;
Viens, Patrice ;
Birnbaum, Daniel .
INTERNATIONAL JOURNAL OF CANCER, 2008, 123 (01) :236-240
[10]   Use of statins and breast cancer: A meta-analysis of seven randomized clinical trials and nine observational studies [J].
Bonovas, S ;
Filioussi, K ;
Tsavaris, N ;
Sitaras, NM .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (34) :8606-8612