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Crosstalk of Long Non-coding RNAs and EMT: Searching the Missing Pieces of an Incomplete Puzzle for Lung Cancer Therapy

Authors :
Shahinozzaman
Ali Zarrabi
Kiavash Hushmandi
Sima Orouei
Milad Ashrafizadeh
Vahideh Zarrin
Anuj Kumar
Masoud Najafi
Farid Hashemi
Saeed Samarghandian
Source :
Current Cancer Drug Targets. 21:640-665
Publication Year :
2021
Publisher :
Bentham Science Publishers Ltd., 2021.

Abstract

Background: Lung cancer has the first place among cancer-related deaths worldwide and demands novel strategies in the treatment of this life-threatening disorder. The aim of this review is to explore the regulation of epithelial-to-mesenchymal transition (EMT) by long non-coding RNAs (lncRNAs) in lung cancer. Introduction: LncRNAs can be considered as potential factors for targeting in cancer therapy, since they regulate a bunch of biological processes, e.g. cell proliferation, differentiation and apoptosis. The abnormal expression of lncRNAs occurs in different cancer cells. On the other hand, epithelial-to-mesenchymal transition (EMT) is a critical mechanism participating in migration and metastasis of cancer cells. Method: Different databases, including Google Scholar, Pubmed and Science direct, were searched for collecting articles using keywords such as “LncRNA”, “EMT”, and “Lung cancer”. Results: There are tumor-suppressing lncRNAs that can suppress EMT and metastasis of lung cancer cells. Expression of such lncRNAs undergoes down-regulation in lung cancer progression and restoring their expression is of importance in suppressing lung cancer migration. There are tumor- promoting lncRNAs triggering EMT in lung cancer and enhancing their migration. Conclusion: LncRNAs are potential regulators of EMT in lung cancer, and targeting them, both pharmacologically and genetically, can be of importance in controlling the migration of lung cancer cells.

Details

ISSN :
15680096
Volume :
21
Database :
OpenAIRE
Journal :
Current Cancer Drug Targets
Accession number :
edsair.doi.dedup.....1a908f7b010c96d28bc96d3152450af0
Full Text :
https://doi.org/10.2174/1568009621666210203110305