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The Potential Links between lncRNAs and Drug Tolerance in Lung Adenocarcinoma. | LitMetric

The Potential Links between lncRNAs and Drug Tolerance in Lung Adenocarcinoma.

Genes (Basel)

Department of Pathology, Dunedin School of Medicine, University of Otago, P.O. Box 56, Dunedin 9054, New Zealand.

Published: July 2024

AI Article Synopsis

  • Lung cancer patients often initially respond to targeted therapies, but many experience relapses due to drug resistance driven by a group of cells called drug-tolerant persisters (DTPs).
  • DTPs enter a dormant state that helps them survive treatment and display traits similar to stem cells, along with notable changes in their genetics and metabolism.
  • While much research has focused on protein coding changes in DTPs, this review discusses the potential significance of long non-coding RNAs (lncRNAs) in understanding drug tolerance and genetic resistance in lung adenocarcinoma.

Article Abstract

Lung cancer patients treated with targeted therapies frequently respond well but invariably relapse due to the development of drug resistance. Drug resistance is in part mediated by a subset of cancer cells termed "drug-tolerant persisters" (DTPs), which enter a dormant, slow-cycling state that enables them to survive drug exposure. DTPs also exhibit stem cell-like characteristics, broad epigenetic reprogramming, altered metabolism, and a mutagenic phenotype mediated by adaptive mutability. While several studies have characterised the transcriptional changes that lead to the altered phenotypes exhibited in DTPs, these studies have focused predominantly on protein coding changes. As long non-coding RNAs (lncRNAs) are also implicated in the phenotypes altered in DTPs, it is likely that they play a role in the biology of drug tolerance. In this review, we outline how lncRNAs may contribute to the key characteristics of DTPs, their potential roles in tolerance to targeted therapies, and the emergence of genetic resistance in lung adenocarcinoma.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11276205PMC
http://dx.doi.org/10.3390/genes15070906DOI Listing

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