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...
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creator | 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 |
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. |
doi_str_mv | 10.1038/s41419-019-1544-y |
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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.</description><identifier>ISSN: 2041-4889</identifier><identifier>EISSN: 2041-4889</identifier><identifier>DOI: 10.1038/s41419-019-1544-y</identifier><identifier>PMID: 30975976</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>38/1 ; 38/39 ; 38/77 ; 38/91 ; 631/337/641/83 ; 631/67/2327 ; 631/80/83 ; 82/58 ; 96/95 ; Acid production ; Adaptor Proteins, Signal Transducing - drug effects ; Adaptor Proteins, Signal Transducing - genetics ; Adaptor Proteins, Signal Transducing - metabolism ; Amino acids ; Amino Acids - metabolism ; Antibodies ; Biochemistry ; Biomedical and Life Sciences ; Cell Biology ; Cell Culture ; Cell growth ; Cell Line, Tumor ; Cell Proliferation ; Cholesterol ; Colon cancer ; Colonic Neoplasms - drug therapy ; Colonic Neoplasms - genetics ; Colonic Neoplasms - metabolism ; Colorectal cancer ; Energy ; Glucose - metabolism ; Humans ; Immunofluorescence ; Immunology ; Lactic acid ; Life Sciences ; Lovastatin ; Lovastatin - pharmacology ; Mevalonate pathway ; Mevalonic acid ; Mevalonic Acid - metabolism ; Nutrient uptake ; Proteomics ; Signal transduction ; Signal Transduction - drug effects ; Signal Transduction - genetics ; Statins ; Transcription Factors - drug effects ; Transcription Factors - genetics ; Transcription Factors - metabolism ; Tumor cell lines ; Tumorigenesis ; Wnt Signaling Pathway - drug effects ; Wnt Signaling Pathway - genetics</subject><ispartof>Cell death & disease, 2019-04, Vol.10 (4), p.327-327, Article 327</ispartof><rights>The Author(s) 2019</rights><rights>The Author(s) 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c536t-d6721ad1d456e8927a355c9d17b164f56098db8520bc96464d349f7a2ccb4c783</citedby><cites>FETCH-LOGICAL-c536t-d6721ad1d456e8927a355c9d17b164f56098db8520bc96464d349f7a2ccb4c783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459916/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459916/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30975976$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gong, Li</creatorcontrib><creatorcontrib>Xiao, Yi</creatorcontrib><creatorcontrib>Xia, Fan</creatorcontrib><creatorcontrib>Wu, Pei</creatorcontrib><creatorcontrib>Zhao, Tingting</creatorcontrib><creatorcontrib>Xie, Shulin</creatorcontrib><creatorcontrib>Wang, Ran</creatorcontrib><creatorcontrib>Wen, Qiaocheng</creatorcontrib><creatorcontrib>Zhou, Wensu</creatorcontrib><creatorcontrib>Xu, Huilan</creatorcontrib><creatorcontrib>Zhu, Lingyan</creatorcontrib><creatorcontrib>Zheng, Zeqi</creatorcontrib><creatorcontrib>Yang, Tianlun</creatorcontrib><creatorcontrib>Chen, Zihua</creatorcontrib><creatorcontrib>Duan, Qiong</creatorcontrib><title>The mevalonate coordinates energy input and cell proliferation</title><title>Cell death & disease</title><addtitle>Cell Death Dis</addtitle><addtitle>Cell Death Dis</addtitle><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.</description><subject>38/1</subject><subject>38/39</subject><subject>38/77</subject><subject>38/91</subject><subject>631/337/641/83</subject><subject>631/67/2327</subject><subject>631/80/83</subject><subject>82/58</subject><subject>96/95</subject><subject>Acid production</subject><subject>Adaptor Proteins, Signal Transducing - drug effects</subject><subject>Adaptor Proteins, Signal Transducing - genetics</subject><subject>Adaptor Proteins, Signal Transducing - metabolism</subject><subject>Amino acids</subject><subject>Amino Acids - metabolism</subject><subject>Antibodies</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Cell Biology</subject><subject>Cell Culture</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>Cholesterol</subject><subject>Colon cancer</subject><subject>Colonic Neoplasms - 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metabolism</topic><topic>Nutrient uptake</topic><topic>Proteomics</topic><topic>Signal transduction</topic><topic>Signal Transduction - drug effects</topic><topic>Signal Transduction - genetics</topic><topic>Statins</topic><topic>Transcription Factors - drug effects</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><topic>Tumor cell lines</topic><topic>Tumorigenesis</topic><topic>Wnt Signaling Pathway - drug effects</topic><topic>Wnt Signaling Pathway - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gong, Li</creatorcontrib><creatorcontrib>Xiao, Yi</creatorcontrib><creatorcontrib>Xia, Fan</creatorcontrib><creatorcontrib>Wu, Pei</creatorcontrib><creatorcontrib>Zhao, Tingting</creatorcontrib><creatorcontrib>Xie, Shulin</creatorcontrib><creatorcontrib>Wang, Ran</creatorcontrib><creatorcontrib>Wen, Qiaocheng</creatorcontrib><creatorcontrib>Zhou, Wensu</creatorcontrib><creatorcontrib>Xu, Huilan</creatorcontrib><creatorcontrib>Zhu, Lingyan</creatorcontrib><creatorcontrib>Zheng, Zeqi</creatorcontrib><creatorcontrib>Yang, Tianlun</creatorcontrib><creatorcontrib>Chen, Zihua</creatorcontrib><creatorcontrib>Duan, Qiong</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell death & disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gong, Li</au><au>Xiao, Yi</au><au>Xia, Fan</au><au>Wu, Pei</au><au>Zhao, Tingting</au><au>Xie, Shulin</au><au>Wang, Ran</au><au>Wen, Qiaocheng</au><au>Zhou, Wensu</au><au>Xu, Huilan</au><au>Zhu, Lingyan</au><au>Zheng, Zeqi</au><au>Yang, Tianlun</au><au>Chen, Zihua</au><au>Duan, Qiong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The mevalonate coordinates energy input and cell proliferation</atitle><jtitle>Cell death & disease</jtitle><stitle>Cell Death Dis</stitle><addtitle>Cell Death Dis</addtitle><date>2019-04-11</date><risdate>2019</risdate><volume>10</volume><issue>4</issue><spage>327</spage><epage>327</epage><pages>327-327</pages><artnum>327</artnum><issn>2041-4889</issn><eissn>2041-4889</eissn><abstract>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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30975976</pmid><doi>10.1038/s41419-019-1544-y</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 38/1 38/39 38/77 38/91 631/337/641/83 631/67/2327 631/80/83 82/58 96/95 Acid production Adaptor Proteins, Signal Transducing - drug effects Adaptor Proteins, Signal Transducing - genetics Adaptor Proteins, Signal Transducing - metabolism Amino acids Amino Acids - metabolism Antibodies Biochemistry Biomedical and Life Sciences Cell Biology Cell Culture Cell growth Cell Line, Tumor Cell Proliferation Cholesterol Colon cancer Colonic Neoplasms - drug therapy Colonic Neoplasms - genetics Colonic Neoplasms - metabolism Colorectal cancer Energy Glucose - metabolism Humans Immunofluorescence Immunology Lactic acid Life Sciences Lovastatin Lovastatin - pharmacology Mevalonate pathway Mevalonic acid Mevalonic Acid - metabolism Nutrient uptake Proteomics Signal transduction Signal Transduction - drug effects Signal Transduction - genetics Statins Transcription Factors - drug effects Transcription Factors - genetics Transcription Factors - metabolism Tumor cell lines Tumorigenesis Wnt Signaling Pathway - drug effects Wnt Signaling Pathway - genetics |
title | The mevalonate coordinates energy input and cell proliferation |
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