The regulatory role of autophagy-related miRNAs in lung cancer drug resistance.


Journal

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
ISSN: 1950-6007
Titre abrégé: Biomed Pharmacother
Pays: France
ID NLM: 8213295

Informations de publication

Date de publication:
Apr 2022
Historique:
received: 28 01 2022
revised: 14 02 2022
accepted: 17 02 2022
pubmed: 23 2 2022
medline: 26 3 2022
entrez: 22 2 2022
Statut: ppublish

Résumé

Autophagy is conserved cellular machinery that degrades un-usable proteins and cellular components and has a crucial role in the pathogenesis and drug resistance of various diseases such as lung cancer (LC). Multiple types of endogenous molecules (i.e. miRNAs) have been found to regulate multiple biological processes, such as autophagy. Dysfunction of these molecules is associated with the onset and progression of a variety of human malignancies. Several studies had shown that some miRNAs could mediate autophagy activity in LC cells, which would affect drug resistance as a major problem in LC therapy. Therefore, identifying the underlying molecular targets of miRNAs and their function in autophagy pathways could develop new treatment interventions for LC patients. In this review, we will summarize the interplay between miRNAs, autophagy, and drug resistance of LC patients, as well as the genes and molecular pathways that are involved.

Identifiants

pubmed: 35193040
pii: S0753-3322(22)00123-8
doi: 10.1016/j.biopha.2022.112735
pii:
doi:

Substances chimiques

MicroRNAs 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

112735

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Masson SAS.. All rights reserved.

Auteurs

Mahshid Shahverdi (M)

Medical Biotechnology Research Center, Arak University of Medical Sciences, Arak, Iran.

Khalil Hajiasgharzadeh (K)

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Amin Daei Sorkhabi (AD)

Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.

Mahdi Jafarlou (M)

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Maryam Shojaee (M)

Department of Clinical Biochemistry, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Neda Jalili Tabrizi (N)

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Nazila Alizadeh (N)

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Mariacarmela Santarpia (M)

Medical Oncology Unit, Department of Human Pathology "G. Barresi", University of Messina, Messina, Italy.

Oronzo Brunetti (O)

Medical oncology unit, IRCCS Istituto Tumori "Giovanni Paolo II" of Bari, Bari, Italy.

Hossein Safarpour (H)

Cellular and Molecular Research Center, Birjand University of Medical Sciences, Birjand, Iran.

Nicola Silvestris (N)

Medical oncology unit, IRCCS Istituto Tumori "Giovanni Paolo II" of Bari, Bari, Italy; Department of Biomedical Sciences and Human Oncology (DIMO), University of Bari, Bari, Italy. Electronic address: n.silvestris@oncologico.bari.it.

Behzad Baradaran (B)

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Pharmaceutical Analysis Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. Electronic address: baradaranb@tbzmed.ac.ir.

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Classifications MeSH