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DGAT1 protects tumor from lipotoxicity, emerging as a promising metabolic target for cancer therapy
We recently demonstrated that glioblastoma, the most lethal brain cancer, upregulates diacylglycerol O-acyltransferase 1 (DGAT1) to store excess fatty acids into triglycerides to prevent lipotoxicity and promote tumor growth. Targeting DGAT1 resulted in marked tumor cell death by triggering extensiv...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7671038/ https://www.ncbi.nlm.nih.gov/pubmed/33235909 http://dx.doi.org/10.1080/23723556.2020.1805257 |
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author | Cheng, Xiang Geng, Feng Guo, Deliang |
author_facet | Cheng, Xiang Geng, Feng Guo, Deliang |
author_sort | Cheng, Xiang |
collection | PubMed |
description | We recently demonstrated that glioblastoma, the most lethal brain cancer, upregulates diacylglycerol O-acyltransferase 1 (DGAT1) to store excess fatty acids into triglycerides to prevent lipotoxicity and promote tumor growth. Targeting DGAT1 resulted in marked tumor cell death by triggering extensive oxidative stress, indicating that DGAT1 could be a promising target for cancer therapy. |
format | Online Article Text |
id | pubmed-7671038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-76710382020-11-23 DGAT1 protects tumor from lipotoxicity, emerging as a promising metabolic target for cancer therapy Cheng, Xiang Geng, Feng Guo, Deliang Mol Cell Oncol Author’s Views We recently demonstrated that glioblastoma, the most lethal brain cancer, upregulates diacylglycerol O-acyltransferase 1 (DGAT1) to store excess fatty acids into triglycerides to prevent lipotoxicity and promote tumor growth. Targeting DGAT1 resulted in marked tumor cell death by triggering extensive oxidative stress, indicating that DGAT1 could be a promising target for cancer therapy. Taylor & Francis 2020-09-08 /pmc/articles/PMC7671038/ /pubmed/33235909 http://dx.doi.org/10.1080/23723556.2020.1805257 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Author’s Views Cheng, Xiang Geng, Feng Guo, Deliang DGAT1 protects tumor from lipotoxicity, emerging as a promising metabolic target for cancer therapy |
title | DGAT1 protects tumor from lipotoxicity, emerging as a promising metabolic target for cancer therapy |
title_full | DGAT1 protects tumor from lipotoxicity, emerging as a promising metabolic target for cancer therapy |
title_fullStr | DGAT1 protects tumor from lipotoxicity, emerging as a promising metabolic target for cancer therapy |
title_full_unstemmed | DGAT1 protects tumor from lipotoxicity, emerging as a promising metabolic target for cancer therapy |
title_short | DGAT1 protects tumor from lipotoxicity, emerging as a promising metabolic target for cancer therapy |
title_sort | dgat1 protects tumor from lipotoxicity, emerging as a promising metabolic target for cancer therapy |
topic | Author’s Views |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7671038/ https://www.ncbi.nlm.nih.gov/pubmed/33235909 http://dx.doi.org/10.1080/23723556.2020.1805257 |
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