» Articles » PMID: 33803022

A Systematic Review of MicroRNAs Involved in Cervical Cancer Progression

Overview
Journal Cells
Publisher MDPI
Date 2021 Apr 3
PMID 33803022
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

To obtain a better understanding on the role of microRNAs in the progression of cervical cancer, a systematic review was performed to analyze cervical cancer microRNA studies. We provide an overview of the studies investigating microRNA expression in relation to cervical cancer (CC) progression, highlighting their common outcomes and target gene interactions according to the regulatory pathways. To achieve this, we systematically searched through PubMed MEDLINE, EMBASE, and Google Scholar for all articles between April 2010 and April 2020, in accordance with the PICO acronym (participants, interventions, comparisons, outcomes). From 27 published reports, totaling 1721 cases and 1361 noncancerous control tissue samples, 26 differentially expressed microRNAs (DEmiRNAs) were identified in different International Federation of Gynecology and Obstetrics (FIGO) stages of cervical cancer development. It was identified that some of the dysregulated microRNAs were associated with specific stages of cervical cancer development. The results indicated that DEmiRNAs in different stages of cervical cancer were functionally involved in several key hallmarks of cancer, such as evading growth suppressors, enabling replicative immortality, activation of invasion and metastasis, resisting cell death, and sustained proliferative signaling. These dysregulated microRNAs could play an important role in cervical cancer's development. Some of the stage-specific microRNAs can also be used as biomarkers for cancer classification and monitoring the progression of cervical cancer.

Citing Articles

Diagnostics and Therapy for Malignant Tumors.

Tsai C, Wang C, Chang H, Chang P, Chang C, Chu T Biomedicines. 2025; 12(12.

PMID: 39767566 PMC: 11726849. DOI: 10.3390/biomedicines12122659.


The Natural History of Cervical Cancer and the Case for MicroRNAs: Is Human Papillomavirus Infection the Whole Story?.

Palomino-Vizcaino G, Banuelos-Villegas E, Alvarez-Salas L Int J Mol Sci. 2024; 25(23.

PMID: 39684702 PMC: 11641362. DOI: 10.3390/ijms252312991.


Understanding the role of miRNAs in cervical cancer pathogenesis and therapeutic responses.

Chauhan P, Pramodh S, Hussain A, Elsori D, Lakhanpal S, Kumar R Front Cell Dev Biol. 2024; 12:1397945.

PMID: 39263322 PMC: 11387185. DOI: 10.3389/fcell.2024.1397945.


Editorial: Searching for causes of infertility: from pathophysiologic mechanisms to therapeutic strategies.

Kamieniczna M, Olszewska M, Malcher A, Stokowy T, Gunes S Front Genet. 2024; 15:1432026.

PMID: 38988834 PMC: 11233803. DOI: 10.3389/fgene.2024.1432026.


miRNAs that regulate apoptosis in breast cancer and cervical cancer.

Beilankouhi E, Maghsoodi M, Zamani Sani M, Khosroshahi N, Zarezadeh R, Nargesi M Cell Biochem Biophys. 2024; 82(3):1993-2006.

PMID: 38969951 DOI: 10.1007/s12013-024-01405-7.


References
1.
Wang N, Zhou Y, Zheng L, Li H . MiR-31 is an independent prognostic factor and functions as an oncomir in cervical cancer via targeting ARID1A. Gynecol Oncol. 2014; 134(1):129-37. DOI: 10.1016/j.ygyno.2014.04.047. View

2.
Gonzalez-Quintana V, Palma-Berre L, Campos-Parra A, Lopez-Urrutia E, Peralta-Zaragoza O, Vazquez-Romo R . MicroRNAs are involved in cervical cancer development, progression, clinical outcome and improvement treatment response (Review). Oncol Rep. 2015; 35(1):3-12. DOI: 10.3892/or.2015.4369. View

3.
Shan D, Shang Y, Hu T . MicroRNA-411 Inhibits Cervical Cancer Progression by Directly Targeting STAT3. Oncol Res. 2018; 27(3):349-358. PMC: 7848402. DOI: 10.3727/096504018X15247361080118. View

4.
Zhao Y, Wang J, Chen X, Wu Y, Wu Q . Values of three different preoperative regimens in comprehensive treatment for young patients with stage Ib2 cervical cancer. Asian Pac J Cancer Prev. 2012; 13(4):1487-9. DOI: 10.7314/apjcp.2012.13.4.1487. View

5.
Ou R, Zhu L, Zhao L, Li W, Tao F, Lu Y . HPV16 E7-induced upregulation of KDM2A promotes cervical cancer progression by regulating miR-132-radixin pathway. J Cell Physiol. 2018; 234(3):2659-2671. DOI: 10.1002/jcp.27080. View