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PPARα Enhances Cancer Cell Chemotherapy Sensitivity by Autophagy Induction

PPARα (peroxisome-proliferator-activated receptor α) plays a critical role in regulation of inflammation and cancer, while the regulatory mechanism of PPARα on cancer cell autophagy is still unclear. Here we found that PPARα enhanced autophagy in HEK293T, SW480, and Hela cell lines, which was indepe...

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Detalles Bibliográficos
Autores principales: You, Mengli, Gao, Jiaming, Jin, Jianhua, Hou, Yongzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6241347/
https://www.ncbi.nlm.nih.gov/pubmed/30519260
http://dx.doi.org/10.1155/2018/6458537
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author You, Mengli
Gao, Jiaming
Jin, Jianhua
Hou, Yongzhong
author_facet You, Mengli
Gao, Jiaming
Jin, Jianhua
Hou, Yongzhong
author_sort You, Mengli
collection PubMed
description PPARα (peroxisome-proliferator-activated receptor α) plays a critical role in regulation of inflammation and cancer, while the regulatory mechanism of PPARα on cancer cell autophagy is still unclear. Here we found that PPARα enhanced autophagy in HEK293T, SW480, and Hela cell lines, which was independent of PPARα transcription activity. PPARα induced antiapoptotic Bcl2 protein degradation resulting in release of the Beclin-1/VPS34 complex. Consistently, silenced PPARα reversed this event. PPARα-induced autophagy significantly inhibited tumor growth and enhanced SW480 cancer cell sensitivity to chemotherapy drugs. Moreover, PPARα agonist increased SW480 cancer cell chemotherapy sensitivity. These findings revealed a novel mechanism of PPARα/Bcl2/autophagy pathway suppressed tumor progression and enhanced chemotherapy sensitivity, which is a potential drug target for cancer treatment.
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spelling pubmed-62413472018-12-05 PPARα Enhances Cancer Cell Chemotherapy Sensitivity by Autophagy Induction You, Mengli Gao, Jiaming Jin, Jianhua Hou, Yongzhong J Oncol Research Article PPARα (peroxisome-proliferator-activated receptor α) plays a critical role in regulation of inflammation and cancer, while the regulatory mechanism of PPARα on cancer cell autophagy is still unclear. Here we found that PPARα enhanced autophagy in HEK293T, SW480, and Hela cell lines, which was independent of PPARα transcription activity. PPARα induced antiapoptotic Bcl2 protein degradation resulting in release of the Beclin-1/VPS34 complex. Consistently, silenced PPARα reversed this event. PPARα-induced autophagy significantly inhibited tumor growth and enhanced SW480 cancer cell sensitivity to chemotherapy drugs. Moreover, PPARα agonist increased SW480 cancer cell chemotherapy sensitivity. These findings revealed a novel mechanism of PPARα/Bcl2/autophagy pathway suppressed tumor progression and enhanced chemotherapy sensitivity, which is a potential drug target for cancer treatment. Hindawi 2018-11-04 /pmc/articles/PMC6241347/ /pubmed/30519260 http://dx.doi.org/10.1155/2018/6458537 Text en Copyright © 2018 Mengli You et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
You, Mengli
Gao, Jiaming
Jin, Jianhua
Hou, Yongzhong
PPARα Enhances Cancer Cell Chemotherapy Sensitivity by Autophagy Induction
title PPARα Enhances Cancer Cell Chemotherapy Sensitivity by Autophagy Induction
title_full PPARα Enhances Cancer Cell Chemotherapy Sensitivity by Autophagy Induction
title_fullStr PPARα Enhances Cancer Cell Chemotherapy Sensitivity by Autophagy Induction
title_full_unstemmed PPARα Enhances Cancer Cell Chemotherapy Sensitivity by Autophagy Induction
title_short PPARα Enhances Cancer Cell Chemotherapy Sensitivity by Autophagy Induction
title_sort pparα enhances cancer cell chemotherapy sensitivity by autophagy induction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6241347/
https://www.ncbi.nlm.nih.gov/pubmed/30519260
http://dx.doi.org/10.1155/2018/6458537
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