Prohibitin promotes androgen receptor activation in ER-positive breast cancer

被引:18
作者
Liu, Pengying [1 ]
Xu, Yumei [1 ]
Zhang, Wenwen [2 ]
Li, Yan [1 ]
Tang, Lin [2 ]
Chen, Weiwei [2 ]
Xu, Jing [2 ]
Sun, Qian [2 ]
Guan, Xiaoxiang [1 ,2 ]
机构
[1] Southern Med Univ, Sch Med, Jinling Hosp, Dept Med Oncol, Guangzhou, Guangdong, Peoples R China
[2] Nanjing Univ, Jinling Hosp, Dept Med Oncol, Sch Med, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
androgen receptor; AR; breast cancer; PHB; prohibitin; PROSTATE-CANCER; TRANSCRIPTIONAL REPRESSION; PROLIFERATION; TUMORS; SUPPRESSION; EXPRESSION; NUCLEUS; CELLS; P53;
D O I
10.1080/15384101.2017.1295193
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Prohibitin (PHB) is an evolutionarily conserved protein with multiple functions in both normal and cancer cells. Androgen receptor (AR) was reported to act as a different role in the ER-positive and ER-negative breast cancer. However, little is known about the role of PHB and whether PHB could regulate AR expression in the ER-positive breast cancer. Here, we determined the expression and clinical outcomes of PHB in breast cancer samples using 121 breast cancer tissues and published databases, and investigated the role of PHB in breast cancer cell growth, apoptosis and cell cycle arrest in the ER-positive breast cancer cells. We obtained the expression of PHB is significantly low in breast cancer samples, and low PHB expression positively correlated with poor prognosis of breast cancer. We detected that PHB could inhibit breast cancer cell proliferation, change cell cycle distribution and promote cell apoptosis in the ER-positive breast cancer cells. Moreover, we found PHB could significantly increase AR expression in both mRNA and protein levels in the ER-positive breast cancer cells. Additionally, a significant positive correlation between PHB and AR expression was identified in the 121 breast cancer tissues. PHB and AR expression are associated with prognosis in the ER-positive breast cancer patients. Our results indicate that PHB promotes AR activation in ER-positive breast cancer, making PHB and AR potential molecular targets for ER-positive breast cancer therapy.
引用
收藏
页码:776 / 784
页数:9
相关论文
共 29 条
[1]   Skp2B attenuates p53 function by inhibiting prohibitin [J].
Chander, Harish ;
Halpern, Max ;
Resnick-Silverman, Lois ;
Manfredi, James J. ;
Germain, Doris .
EMBO REPORTS, 2010, 11 (03) :220-225
[2]   Prohibitin interacts with RNF2 and regulates E2F1 function via dual pathways [J].
Choi, D. ;
Lee, S-J ;
Hong, S. ;
Kim, I-H ;
Kang, S. .
ONCOGENE, 2008, 27 (12) :1716-1725
[3]   The prohibitin family of mitochondrial proteins regulate replicative lifespan [J].
Coates, PJ ;
Jamieson, DJ ;
Smart, K ;
Prescott, AR ;
Hall, PA .
CURRENT BIOLOGY, 1997, 7 (08) :607-610
[4]   Prohibitin and the SWI/SNF ATPase subunit BRG1 are required for effective androgen antagonist-mediated transcriptional repression of androgen receptor-regulated genes [J].
Dai, Yan ;
Ngo, Duyen ;
Jacob, Johanna ;
Forman, Lora W. ;
Faller, Douglas V. .
CARCINOGENESIS, 2008, 29 (09) :1725-1733
[5]   Reducing prohibitin increases histone acetylation, and promotes androgen independence in prostate tumours by increasing androgen receptor activation by adrenal androgens [J].
Dart, D. A. ;
Brooke, G. N. ;
Sita-Lumsden, A. ;
Waxman, J. ;
Bevan, C. L. .
ONCOGENE, 2012, 31 (43) :4588-4598
[6]   Manipulating prohibitin levels provides evidence for an in vivo role in androgen regulation of prostate tumours [J].
Dart, D. Alwyn ;
Spencer-Dene, Bradley ;
Gamble, Simon C. ;
Waxman, Jonathan ;
Bevan, Charlotte L. .
ENDOCRINE-RELATED CANCER, 2009, 16 (04) :1157-1169
[7]   The development of androgen-independent prostate cancer [J].
Feldman, BJ ;
Feldman, D .
NATURE REVIEWS CANCER, 2001, 1 (01) :34-45
[8]   Androgen-regulated processing of the oncomir MiR-27a, which targets Prohibitin in prostate cancer [J].
Fletcher, Claire E. ;
Dart, D. Alwyn ;
Sita-Lumsden, Ailsa ;
Cheng, Helen ;
Rennie, Paul S. ;
Bevan, Charlotte L. .
HUMAN MOLECULAR GENETICS, 2012, 21 (14) :3112-3127
[9]   Prohibitin induces the transcriptional activity of p53 and is exported from the nucleus upon apoptotic signaling [J].
Fusaro, G ;
Dasgupta, P ;
Rastogi, S ;
Joshi, B ;
Chellappan, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (48) :47853-47861
[10]   Androgens target prohibitin to regulate proliferation of prostate cancer cells [J].
Gamble, SC ;
Odontiadis, M ;
Waxman, J ;
Westbrook, JA ;
Dunn, MJ ;
Wait, R ;
Lam, EWF ;
Bevan, CL .
ONCOGENE, 2004, 23 (17) :2996-3004