MicroRNAs in gynecological cancers: Small molecules with big implications

被引:81
作者
Srivastava, Sanjeev K. [1 ]
Ahmad, Aamir [1 ]
Zubair, Haseeb [1 ]
Miree, Orlandric [1 ]
Singh, Seema [1 ,2 ]
Rocconi, Rodney P. [3 ]
Scalici, Jennifer [3 ]
Singh, Ajay P. [1 ,2 ]
机构
[1] Univ S Alabama, Mitchell Canc Inst, Dept Oncol Sci, 1660 Springhill Ave, Mobile, AL 36604 USA
[2] Univ S Alabama, Coll Med, Dept Biochem & Mol Biol, Mobile, AL 36688 USA
[3] Univ S Alabama, Mitchell Canc Inst, Div Gynecol Oncol, Mobile, AL 36604 USA
关键词
MicroRNAs; Gynecological cancers; Ovarian cancer; Endometrial cancer; Cervical cancer; Tumor microenvironment; HUMAN OVARIAN-CANCER; EPITHELIAL-MESENCHYMAL TRANSITION; HUMAN CERVICAL-CANCER; PROMOTES CELL-PROLIFERATION; SUPPRESSES TUMOR-GROWTH; LYMPH-NODE METASTASIS; DEATH; PDCD4; ENDOMETRIAL CANCER; DOWN-REGULATION; CISPLATIN-RESISTANCE;
D O I
10.1016/j.canlet.2017.05.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gynecological cancers (GCs) are often diagnosed at advanced stages, limiting the efficacy of available therapeutic options. Thus, there remains an urgent and unmet need for innovative research for the efficient clinical management of GC patients. Research over past several years has revealed the enormous promise of miRNAs. These small non-coding RNAs can aid in the diagnosis, prognosis and therapy of all major GCs, viz., ovarian cancers, cervical cancers and endometrial cancers. Mechanistic details of the miRNAs-mediated regulation of multiple biological functions are under constant investigation, and a number of miRNAs are now believed to influence growth, proliferation, invasion, metastasis, chemoresistance and the relapse of different GCs. Modulation of tumor microenvironment by miRNAs can possibly explain some of their reported biological effects. miRNA signatures have been proposed as biomarkers for the early detection of GCs, even the various subtypes of individual GCs. miRNA signatures are also being pursued as predictors of response to therapies. This review catalogs the knowledge gained from collective studies, so as to assess the progress made so far. It is time to ponder over the knowledge gained, so that more meaningful pre-clinical and translational studies can be designed to better realize the potential that miRNAs have to offer. Published by Elsevier Ireland Ltd.
引用
收藏
页码:123 / 138
页数:16
相关论文
共 329 条
[1]   Phosphoglucose Isomerase/Autocrine Motility Factor Mediates Epithelial-Mesenchymal Transition Regulated by miR-200 in Breast Cancer Cells [J].
Ahmad, Aamir ;
Aboukameel, Amro ;
Kong, Dejuan ;
Wang, Zhiwei ;
Sethi, Seema ;
Chen, Wei ;
Sarkar, Fazlul H. ;
Raz, Avraham .
CANCER RESEARCH, 2011, 71 (09) :3400-3409
[2]  
[Anonymous], NATURE
[3]  
[Anonymous], J CLIN PATHOL
[4]  
[Anonymous], ONCOL RES
[5]  
[Anonymous], BIOCH BIOPHYS RES CO
[6]  
[Anonymous], PLOS ONE
[7]  
[Anonymous], ONCOGENE
[8]   Silencing of miR-148a in cancer-associated fibroblasts results in WNT10B-mediated stimulation of tumor cell motility [J].
Aprelikova, O. ;
Palla, J. ;
Hibler, B. ;
Yu, X. ;
Greer, Y. E. ;
Yi, M. ;
Stephens, R. ;
Maxwell, G. L. ;
Jazaeri, A. ;
Risinger, J. I. ;
Rubin, J. S. ;
Niederhuber, J. .
ONCOGENE, 2013, 32 (27) :3246-3253
[9]   Evolving role of uPA/uPAR system in human cancers [J].
Ass, Kathleen ;
Ahmad, Aamir ;
Azmi, Asfar S. ;
Sarkar, Sarah H. ;
Sarkar, Fazlul H. .
CANCER TREATMENT REVIEWS, 2008, 34 (02) :122-136
[10]   Early detection of ovarian cancer [J].
Badgwell, Donna ;
Bast, Robert C., Jr. .
DISEASE MARKERS, 2007, 23 (5-6) :397-410