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CRISPR-Induced Loss of Connexin 43 Expression Sensitizes KRAS Mutant Cells to Cisplatin
Gap Junction intercellular communication (GJIC) is often dysregulated in cancers, and this dysregulation has been shown to have pro-tumorigenic effects. Connexins (Cxs) are transmembrane proteins that make up gap junctions. Previous studies have indicated that RNA interference (RNAi)-based suppressi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Caltech Library
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9701319/ https://www.ncbi.nlm.nih.gov/pubmed/36447529 http://dx.doi.org/10.17912/micropub.biology.000681 |
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author | Martin, Stephen Mu, David |
author_facet | Martin, Stephen Mu, David |
author_sort | Martin, Stephen |
collection | PubMed |
description | Gap Junction intercellular communication (GJIC) is often dysregulated in cancers, and this dysregulation has been shown to have pro-tumorigenic effects. Connexins (Cxs) are transmembrane proteins that make up gap junctions. Previous studies have indicated that RNA interference (RNAi)-based suppression of Cx43 increases cellular resistance to the chemotherapeutic agent cisplatin. Interestingly, we found that the loss of Cx43 expression induced by the CRISPR-Cas9 technology sensitizes cells to cisplatin in a KRAS mutant-dependent manner. |
format | Online Article Text |
id | pubmed-9701319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Caltech Library |
record_format | MEDLINE/PubMed |
spelling | pubmed-97013192022-11-28 CRISPR-Induced Loss of Connexin 43 Expression Sensitizes KRAS Mutant Cells to Cisplatin Martin, Stephen Mu, David MicroPubl Biol New Finding Gap Junction intercellular communication (GJIC) is often dysregulated in cancers, and this dysregulation has been shown to have pro-tumorigenic effects. Connexins (Cxs) are transmembrane proteins that make up gap junctions. Previous studies have indicated that RNA interference (RNAi)-based suppression of Cx43 increases cellular resistance to the chemotherapeutic agent cisplatin. Interestingly, we found that the loss of Cx43 expression induced by the CRISPR-Cas9 technology sensitizes cells to cisplatin in a KRAS mutant-dependent manner. Caltech Library 2022-11-13 /pmc/articles/PMC9701319/ /pubmed/36447529 http://dx.doi.org/10.17912/micropub.biology.000681 Text en Copyright: © 2022 by the authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | New Finding Martin, Stephen Mu, David CRISPR-Induced Loss of Connexin 43 Expression Sensitizes KRAS Mutant Cells to Cisplatin |
title | CRISPR-Induced Loss of Connexin 43 Expression Sensitizes KRAS Mutant Cells to Cisplatin |
title_full | CRISPR-Induced Loss of Connexin 43 Expression Sensitizes KRAS Mutant Cells to Cisplatin |
title_fullStr | CRISPR-Induced Loss of Connexin 43 Expression Sensitizes KRAS Mutant Cells to Cisplatin |
title_full_unstemmed | CRISPR-Induced Loss of Connexin 43 Expression Sensitizes KRAS Mutant Cells to Cisplatin |
title_short | CRISPR-Induced Loss of Connexin 43 Expression Sensitizes KRAS Mutant Cells to Cisplatin |
title_sort | crispr-induced loss of connexin 43 expression sensitizes kras mutant cells to cisplatin |
topic | New Finding |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9701319/ https://www.ncbi.nlm.nih.gov/pubmed/36447529 http://dx.doi.org/10.17912/micropub.biology.000681 |
work_keys_str_mv | AT martinstephen crisprinducedlossofconnexin43expressionsensitizeskrasmutantcellstocisplatin AT mudavid crisprinducedlossofconnexin43expressionsensitizeskrasmutantcellstocisplatin |