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LncRNAs link cancer stemness to therapy resistance.

Authors :
Yue J
Wu Y
Qiu L
Zhao R
Jiang M
Zhang H
Source :
American journal of cancer research [Am J Cancer Res] 2021 Apr 15; Vol. 11 (4), pp. 1051-1068. Date of Electronic Publication: 2021 Apr 15 (Print Publication: 2021).
Publication Year :
2021

Abstract

Cancer stem cells (CSCs) are a cellular subpopulation accelerating cancer cell growth, invasion and metastasis and survival. After chemoradiotherapy, CSCs are enriched because of their survival advantages and lead to tumor relapse and metastasis. Elimination of CSCs is critically important for the radical treatment of human cancers. Long non-coding RNAs (lncRNAs) are a group of RNAs longer than 200 nucleotides and have no protein-coding potential. Aberrant expressions of lncRNAs are associated with human diseases including cancer. LncRNAs function as cancer biomarkers, prognostic factors and therapeutic targets. They induce cancer stemness by chromatin modification, transcriptional regulation or post-transcriptional regulation of target genes as a sponge or through assembling a scaffold complex. Several factors caused aberrant expressions of lncRNAs in CSCs such as genes mutations, epigenetic alteration and environmental stimuli. Targeting of lncRNAs has been demonstrated to significantly reverse the chemoradioresistance of CSCs. In this review, we have summarized the progress of studies regarding lncRNAs-mediated therapy resistance of CSCs and clarified the molecular mechanisms. Furthermore, we have for the first time analyzed the influences of lncRNAs on cell metabolism and emphasized the effect of tumor microenvironment on lncRNAs functions in CSCs. Overall, the thorough understanding of the association of lncRNAs and CSCs would contribute to the reversal of therapy resistance.<br />Competing Interests: None.<br /> (AJCR Copyright © 2021.)

Details

Language :
English
ISSN :
2156-6976
Volume :
11
Issue :
4
Database :
MEDLINE
Journal :
American journal of cancer research
Publication Type :
Academic Journal
Accession number :
33948345