Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2017 Oct 28:407:123-138.
doi: 10.1016/j.canlet.2017.05.011. Epub 2017 May 24.

MicroRNAs in gynecological cancers: Small molecules with big implications

Affiliations
Review

MicroRNAs in gynecological cancers: Small molecules with big implications

Sanjeev K Srivastava et al. Cancer Lett. .

Abstract

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.

Keywords: Cervical cancer; Endometrial cancer; Gynecological cancers; MicroRNAs; Ovarian cancer; Tumor microenvironment.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest: APS and SS are co-founders and serve on executive management team of Tatva Biosciences LLC, which is involved in the development of tools and models for cancer health disparity research. SKS serves as the Director of Cell Biology and Genetics at Tatva Biosciences LLC.

Figures

Figure 1
Figure 1

References

    1. Bourla AB, Zamarin D. Immunotherapy: New Strategies for the Treatment of Gynecologic Malignancies. Oncology (Williston Park) 2016;30:59–66. 69. - PMC - PubMed
    1. Collins Y, Holcomb K, Chapman-Davis E, Khabele D, Farley JH. Gynecologic cancer disparities: a report from the Health Disparities Taskforce of the Society of Gynecologic Oncology. Gynecologic oncology. 2014;133:353–361. - PMC - PubMed
    1. Jonas S, Izaurralde E. Towards a molecular understanding of microRNA-mediated gene silencing. Nat Rev Genet. 2015;16:421–433. - PubMed
    1. Zhong X, Coukos G, Zhang L. miRNAs in human cancer. Methods Mol Biol. 2012;822:295–306. - PMC - PubMed
    1. Siegel RL, Miller KD, Jemal A. Cancer Statistics, 2017. CA Cancer J Clin. 2017;67:7–30. - PubMed

Publication types

MeSH terms