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The mevalonate coordinates energy input and cell proliferation
The mevalonate pathway is known for the synthesis of cholesterol, but recent studies have reported that it also controls Hippo signaling, which is critical for the regulation of organ size and tumorigenesis. Here, we discover that the suppression of the mevalonate pathway inhibits the growth and pro...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459916/ https://www.ncbi.nlm.nih.gov/pubmed/30975976 http://dx.doi.org/10.1038/s41419-019-1544-y |
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author | Gong, Li Xiao, Yi Xia, Fan Wu, Pei Zhao, Tingting Xie, Shulin Wang, Ran Wen, Qiaocheng Zhou, Wensu Xu, Huilan Zhu, Lingyan Zheng, Zeqi Yang, Tianlun Chen, Zihua Duan, Qiong |
author_facet | Gong, Li Xiao, Yi Xia, Fan Wu, Pei Zhao, Tingting Xie, Shulin Wang, Ran Wen, Qiaocheng Zhou, Wensu Xu, Huilan Zhu, Lingyan Zheng, Zeqi Yang, Tianlun Chen, Zihua Duan, Qiong |
author_sort | Gong, Li |
collection | PubMed |
description | The mevalonate pathway is known for the synthesis of cholesterol, but recent studies have reported that it also controls Hippo signaling, which is critical for the regulation of organ size and tumorigenesis. Here, we discover that the suppression of the mevalonate pathway inhibits the growth and proliferation of colon cancer cell lines. The results of transcriptomic and proteomic assays suggested that the mevalonate pathway controls multiple signaling pathways relevant to cell proliferation, and the results were further confirmed using western blot, PCR, and immunofluorescence assays. As cell proliferation is an energy-consuming process, we postulate that the mevalonate pathway may also control nutrient uptake to coordinate the processes of energy supply and cell proliferation. Here, we found that lovastatin, a mevalonate pathway inhibitor, suppresses glucose and amino acid uptake and lactate acid production. More importantly, mevalonic acid itself is sufficient to promote glucose uptake by colon cancer cells. In addition, we found that colon cancer tissues displayed a higher expression of mevalonate pathway enzymes, which may promote cell growth and stimulate energy uptake. Together, our findings establish the mevalonate pathway as a critical regulator in coordinating energy input and cell proliferation. |
format | Online Article Text |
id | pubmed-6459916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64599162019-04-15 The mevalonate coordinates energy input and cell proliferation Gong, Li Xiao, Yi Xia, Fan Wu, Pei Zhao, Tingting Xie, Shulin Wang, Ran Wen, Qiaocheng Zhou, Wensu Xu, Huilan Zhu, Lingyan Zheng, Zeqi Yang, Tianlun Chen, Zihua Duan, Qiong Cell Death Dis Article The mevalonate pathway is known for the synthesis of cholesterol, but recent studies have reported that it also controls Hippo signaling, which is critical for the regulation of organ size and tumorigenesis. Here, we discover that the suppression of the mevalonate pathway inhibits the growth and proliferation of colon cancer cell lines. The results of transcriptomic and proteomic assays suggested that the mevalonate pathway controls multiple signaling pathways relevant to cell proliferation, and the results were further confirmed using western blot, PCR, and immunofluorescence assays. As cell proliferation is an energy-consuming process, we postulate that the mevalonate pathway may also control nutrient uptake to coordinate the processes of energy supply and cell proliferation. Here, we found that lovastatin, a mevalonate pathway inhibitor, suppresses glucose and amino acid uptake and lactate acid production. More importantly, mevalonic acid itself is sufficient to promote glucose uptake by colon cancer cells. In addition, we found that colon cancer tissues displayed a higher expression of mevalonate pathway enzymes, which may promote cell growth and stimulate energy uptake. Together, our findings establish the mevalonate pathway as a critical regulator in coordinating energy input and cell proliferation. Nature Publishing Group UK 2019-04-11 /pmc/articles/PMC6459916/ /pubmed/30975976 http://dx.doi.org/10.1038/s41419-019-1544-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Gong, Li Xiao, Yi Xia, Fan Wu, Pei Zhao, Tingting Xie, Shulin Wang, Ran Wen, Qiaocheng Zhou, Wensu Xu, Huilan Zhu, Lingyan Zheng, Zeqi Yang, Tianlun Chen, Zihua Duan, Qiong The mevalonate coordinates energy input and cell proliferation |
title | The mevalonate coordinates energy input and cell proliferation |
title_full | The mevalonate coordinates energy input and cell proliferation |
title_fullStr | The mevalonate coordinates energy input and cell proliferation |
title_full_unstemmed | The mevalonate coordinates energy input and cell proliferation |
title_short | The mevalonate coordinates energy input and cell proliferation |
title_sort | mevalonate coordinates energy input and cell proliferation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459916/ https://www.ncbi.nlm.nih.gov/pubmed/30975976 http://dx.doi.org/10.1038/s41419-019-1544-y |
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