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LncRNA-DANCR: A valuable cancer related long non-coding RNA for human cancers.

Authors :
Thin KZ
Liu X
Feng X
Raveendran S
Tu JC
Source :
Pathology, research and practice [Pathol Res Pract] 2018 Jun; Vol. 214 (6), pp. 801-805. Date of Electronic Publication: 2018 Apr 24.
Publication Year :
2018

Abstract

Objectives: Long noncoding RNAs (lncRNA) are a type of noncoding RNA that comprise of longer than 200 nucleotides sequences. They can regulate chromosome structure, gene expression and play an essential role in the pathophysiology of human diseases, especially in tumorigenesis and progression. Nowadays, they are being targeted as potential biomarkers for various cancer types. And many research studies have proven that lncRNAs might bring a new era to cancer diagnosis and support treatment management. The purpose of this review was to inspect the molecular mechanism and clinical significance of long non-coding RNA- differentiation antagonizing nonprotein coding RNA(DANCR) in various types of human cancers.<br />Materials and Methods: In this review, we summarize and figure out recent research studies concerning the expression and biological mechanisms of lncRNA-DANCR in tumour development. The related studies were obtained through a systematic search of PubMed, Embase and Cochrane Library.<br />Results: Long non-coding RNAs-DANCR is a valuable cancer-related lncRNA that its dysregulated expression was found in a variety of malignancies, including hepatocellular carcinoma, breast cancer, glioma, colorectal cancer, gastric cancer, and lung cancer. The aberrant expressions of DANCR have been shown to contribute to proliferation, migration and invasion of cancer cells.<br />Conclusions: Long non-coding RNAs-DANCR likely serves as a useful disease biomarker or therapeutic cancer target.<br /> (Copyright © 2018 Elsevier GmbH. All rights reserved.)

Details

Language :
English
ISSN :
1618-0631
Volume :
214
Issue :
6
Database :
MEDLINE
Journal :
Pathology, research and practice
Publication Type :
Academic Journal
Accession number :
29728310
Full Text :
https://doi.org/10.1016/j.prp.2018.04.003