» Articles » PMID: 33375067

MiR-205 in Breast Cancer: State of the Art

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2020 Dec 30
PMID 33375067
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

Despite its controversial roles in different cancer types, miR-205 has been mainly described as an oncosuppressive microRNA (miRNA), with some contrasting results, in breast cancer. The role of miR-205 in the occurrence or progression of breast cancer has been extensively studied since the first evidence of its aberrant expression in tumor tissues versus normal counterparts. To date, it is known that the expression of miR-205 in the different subtypes of breast cancer is decreasing from the less aggressive subtype, estrogen receptor/progesterone receptor positive breast cancer, to the more aggressive, triple negative breast cancer, influencing metastasis capability, response to therapy and patient survival. In this review, we summarize the most important discoveries that have highlighted the functional role of this miRNA in breast cancer initiation and progression, in stemness maintenance, in the tumor microenvironment, its potential role as a biomarker and its relevance in normal breast physiology-the still open questions. Finally, emerging evidence reveals the role of some lncRNAs in breast cancer progression as sponges of miR-205. Here, we also reviewed the studies in this field.

Citing Articles

miR-205 Regulates Tamoxifen Resistance by Targeting Estrogen Receptor Coactivator MED1 in Human Breast Cancer.

Ouyang B, Bi M, Jadhao M, Bick G, Zhang X Cancers (Basel). 2024; 16(23.

PMID: 39682180 PMC: 11640040. DOI: 10.3390/cancers16233992.


Evaluation of tumorigenesis-related miRNAs in breast cancer in Egyptian women: a retrospective, exploratory analysis.

Salum G, Elaraby N, Ahmed H, Abd El Meguid M, Fotouh B, Ashraf M Sci Rep. 2024; 14(1):29757.

PMID: 39614097 PMC: 11607072. DOI: 10.1038/s41598-024-68758-0.


Modulation of miR-205 expression using a phyto-nano hybrid as a potential therapeutic agent against breast cancer.

Razzaq F, Shahid S, Shahid W RSC Adv. 2024; 14(50):37286-37298.

PMID: 39575377 PMC: 11580155. DOI: 10.1039/d4ra03069a.


An ultrasensitive electrochemical biosensor with dual-amplification mode and enzyme-deposited silver for detection of miR-205-5p.

Xie X, Chen C, Chen W, Qin Y, Xiang S, Jiang J Mikrochim Acta. 2024; 191(9):545.

PMID: 39158763 DOI: 10.1007/s00604-024-06596-7.


Nanoliposomes as nonviral vectors in cancer gene therapy.

Yildiz S, Entezari M, Paskeh M, Mirzaei S, Kalbasi A, Zabolian A MedComm (2020). 2024; 5(7):e583.

PMID: 38919334 PMC: 11199024. DOI: 10.1002/mco2.583.


References
1.
Hu Y, Qiu Y, Yague E, Ji W, Liu J, Zhang J . miRNA-205 targets VEGFA and FGF2 and regulates resistance to chemotherapeutics in breast cancer. Cell Death Dis. 2016; 7(6):e2291. PMC: 5108343. DOI: 10.1038/cddis.2016.194. View

2.
Grelet S, Link L, Howley B, Obellianne C, Palanisamy V, Gangaraju V . A regulated PNUTS mRNA to lncRNA splice switch mediates EMT and tumour progression. Nat Cell Biol. 2017; 19(9):1105-1115. PMC: 5578890. DOI: 10.1038/ncb3595. View

3.
Zhang P, Wang L, Rodriguez-Aguayo C, Yuan Y, Debeb B, Chen D . miR-205 acts as a tumour radiosensitizer by targeting ZEB1 and Ubc13. Nat Commun. 2014; 5:5671. PMC: 4377070. DOI: 10.1038/ncomms6671. View

4.
Yang Y, Xun N, Wu J . Long non-coding RNA FGF14-AS2 represses proliferation, migration, invasion, and induces apoptosis in breast cancer by sponging miR-205-5p. Eur Rev Med Pharmacol Sci. 2019; 23(16):6971-6982. DOI: 10.26355/eurrev_201908_18737. View

5.
Fan X, Chen W, Fu Z, Zeng L, Yin Y, Yuan H . MicroRNAs, a subpopulation of regulators, are involved in breast cancer progression through regulating breast cancer stem cells. Oncol Lett. 2017; 14(5):5069-5076. PMC: 5666663. DOI: 10.3892/ol.2017.6867. View