Crosstalk between long non-coding RNA DLX6-AS1, microRNAs and signaling pathways: A pivotal molecular mechanism in human cancers.


Journal

Gene
ISSN: 1879-0038
Titre abrégé: Gene
Pays: Netherlands
ID NLM: 7706761

Informations de publication

Date de publication:
15 Feb 2021
Historique:
received: 27 05 2020
revised: 02 09 2020
accepted: 07 10 2020
pubmed: 16 10 2020
medline: 30 1 2021
entrez: 15 10 2020
Statut: ppublish

Résumé

Long non-coding RNAs (lncRNAs) are a type of non-protein coding RNA, which have been found to play multiple roles in various molecular and cellular processes by epigenetic regulation of gene expression at post transcriptional levels. LncRNAs may act either as an oncogene or as a tumor suppressor gene in different cancers. Aberrant expression and dysregulation of lncRNAs has been correlated with cancer development and tumor growth via several different signaling pathways. Therefore, lncRNAs could serve as diagnostic biomarkers and as therapeutic targetes in many human cancers. Previous studies have reported that dysregulated expression of the lncRNA called DLX6-AS1 in various cancer types, such as lung, colorectal, bladder, ovarian, hepatocellular, pancreatic and gastric. DLX6-AS1 plays an important role in tumorigenesis by affecting cell proliferation, migration, invasion, EMT, and apoptosis. DLX6-AS1 exerts these regulatory effects by interfering with various microRNA axes and signaling pathways including, Wnt/βcatenin, Notch, P13/AKT/mTOR, and STAT3. This review focuses on the possible mechanisms by which DLX6-AS1 regulates tumor initiation and progression. Accordingly, DLX6-AS1 may act as a novel potential biomarker for cancer diagnosis or therapy in future.

Identifiants

pubmed: 33059027
pii: S0378-1119(20)30893-3
doi: 10.1016/j.gene.2020.145224
pii:
doi:

Substances chimiques

DLX6 protein, human 0
Homeodomain Proteins 0
MicroRNAs 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

145224

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Anita Alizadeh (A)

Department of Biological Science, Faculty of Basic Science, Higher Education Institute of Rab-Rashid, Tabriz, Iran.

Asiyeh Jebelli (A)

Department of Biological Science, Faculty of Basic Science, Higher Education Institute of Rab-Rashid, Tabriz, Iran.

Behzad Baradaran (B)

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

Mohammad Amini (M)

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

Fatemeh Oroojalian (F)

Department of Advanced Sciences and Technologies, North Khorasan University of Medical Sciences, Bojnurd, Iran.

Mahmoud Hashemzaei (M)

Department of Pharmacodynamics and Aptameology, School of Pharmacy, Zabol University of Medical Sciences, Zabol. Iran.

Ahad Mokhtarzadeh (A)

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran. Electronic address: mokhtarzadehah@tbzmed.ac.ir.

Michael R Hamblin (MR)

Wellman Center for Photomedicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, 02114, USA; Laser Research Centre, Faculty of Health Science, University of Johannesburg, Doornfontein 2028, South Africa. Electronic address: hamblin@helix.mgh.harvard.edu.

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Classifications MeSH