4.5 Review

Gastrointestinal cancer drug resistance: the role of exosomal miRNAs

Journal

MOLECULAR BIOLOGY REPORTS
Volume 49, Issue 3, Pages 2421-2432

Publisher

SPRINGER
DOI: 10.1007/s11033-021-07007-3

Keywords

Exosome; miRNA; Exosomal miRNA; Gastrointestinal cancer; Drug resistance

Funding

  1. Abadan University of Medical Sciences, Abadan, Iran [1400U-1251]

Ask authors/readers for more resources

Exosomal miRNAs play crucial roles in drug resistance of GI cancer cells by facilitating cell-to-cell communication through transferring various cargos, providing new insights into understanding the mechanism of drug resistance in GI cancers.
Resistance of gastrointestinal (GI) cancer cells to therapeutic agents are one of the major problems in treating this type of cancer. Although the exact mechanism of drug resistance has not yet been fully elucidated, various factors have been identified as contributing factors involved in this process. Several studies have revealed the role of exosomes, especially exosomal microRNAs (miRNAs), in GI tumorigenesis, invasion, angiogenesis, and drug resistance. Exosomes, a type of small extracellular vesicles (EVs), are originated from endosomes and are released into the extracellular environment and body fluids by different cell types. Exosomes mediate cell-cell communication by transferring different cargos, including miRNAs, between parent and recipient cells. Therefore, identifying these exosomal miRNAs and their functions in GI cancers might provide new clues to further explore the secret of this process and thus help in drug-resistance management. This review article will discuss the roles of exosomal miRNAs and their mechanisms of action in drug resistance of different types of GI cancer cells (e.g., stomach, esophagus, liver, pancreas, and colon) to therapeutic agents.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available