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VDR–SOX2 signaling promotes colorectal cancer stemness and malignancy in an acidic microenvironment
The acidic tumor microenvironment provides an energy source driving malignant tumor progression. Adaptation of cells to an acidic environment leads to the emergence of cancer stem cells. The expression of the vitamin D receptor (VDR) is closely related to the initiation and development of colorectal...
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Published in: | Signal transduction and targeted therapy 2020-09, Vol.5 (1), p.183-183, Article 183 |
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creator | Hu, Pei-Shan Li, Ting Lin, Jin-Fei Qiu, Miao-Zhen Wang, De-Shen Liu, Ze-Xian Chen, Zhan-Hong Yang, Lu-Ping Zhang, Xiao-Long Zhao, Qi Chen, Yan-Xing Lu, Yun-Xin Wu, Qi-Nian Pu, Heng-Ying Zeng, Zhao-Lei Xie, Dan Ju, Huai-Qiang Luo, Hui-Yan Xu, Rui-Hua |
description | The acidic tumor microenvironment provides an energy source driving malignant tumor progression. Adaptation of cells to an acidic environment leads to the emergence of cancer stem cells. The expression of the vitamin D receptor (VDR) is closely related to the initiation and development of colorectal carcinoma (CRC), but its regulatory mechanism in CRC stem cells is still unclear. Our study revealed that acidosis reduced VDR expression by downregulating peroxisome proliferator-activated receptor delta (PPARD) expression. Overexpression of VDR effectively suppressed the stemness and oxaliplatin resistance of cells in acidosis. The nuclear export signal in VDR was sensitive to acidosis, and VDR was exported from the nucleus. Chromatin immunoprecipitation (ChIP) and assay for transposase-accessible chromatin with high-throughput sequencing (ATAC-seq) analyses showed that VDR transcriptionally repressed SRY-box 2 (
SOX2
) by binding to the vitamin D response elements in the promoter of
SOX2
, impairing tumor growth and drug resistance. We demonstrated that a change in the acidic microenvironment combined with overexpression of VDR substantially restricted the occurrence and development of CRC in vivo. These findings reveal a new mechanism by which acidosis could affect the stemness of CRC cells by regulating the expression of SOX2 and show that abnormal VDR expression leads to ineffective activation of vitamin D signaling, resulting in a lack of efficacy of vitamin D in antineoplastic process. |
doi_str_mv | 10.1038/s41392-020-00230-7 |
format | article |
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SOX2
) by binding to the vitamin D response elements in the promoter of
SOX2
, impairing tumor growth and drug resistance. We demonstrated that a change in the acidic microenvironment combined with overexpression of VDR substantially restricted the occurrence and development of CRC in vivo. These findings reveal a new mechanism by which acidosis could affect the stemness of CRC cells by regulating the expression of SOX2 and show that abnormal VDR expression leads to ineffective activation of vitamin D signaling, resulting in a lack of efficacy of vitamin D in antineoplastic process.</description><identifier>ISSN: 2059-3635</identifier><identifier>ISSN: 2095-9907</identifier><identifier>EISSN: 2059-3635</identifier><identifier>DOI: 10.1038/s41392-020-00230-7</identifier><identifier>PMID: 32900990</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/337/176 ; 631/532/71 ; 631/67/1504 ; Acidosis ; Cancer Research ; Cell Biology ; Colorectal cancer ; Internal Medicine ; Medicine ; Medicine & Public Health ; Oncology ; Pathology ; Stem cells ; Vitamin D</subject><ispartof>Signal transduction and targeted therapy, 2020-09, Vol.5 (1), p.183-183, Article 183</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. 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-c474t-547da14a082e87d4580eefefbcbd351e0132f246d67a7e2e999926df81d073f63</citedby><cites>FETCH-LOGICAL-c474t-547da14a082e87d4580eefefbcbd351e0132f246d67a7e2e999926df81d073f63</cites><orcidid>0000-0003-2242-3138 ; 0000-0003-1713-5465 ; 0000-0001-9771-8534</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2440762862/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2440762862?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,25734,27905,27906,36993,36994,44571,53772,53774,74875</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32900990$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hu, Pei-Shan</creatorcontrib><creatorcontrib>Li, Ting</creatorcontrib><creatorcontrib>Lin, Jin-Fei</creatorcontrib><creatorcontrib>Qiu, Miao-Zhen</creatorcontrib><creatorcontrib>Wang, De-Shen</creatorcontrib><creatorcontrib>Liu, Ze-Xian</creatorcontrib><creatorcontrib>Chen, Zhan-Hong</creatorcontrib><creatorcontrib>Yang, Lu-Ping</creatorcontrib><creatorcontrib>Zhang, Xiao-Long</creatorcontrib><creatorcontrib>Zhao, Qi</creatorcontrib><creatorcontrib>Chen, Yan-Xing</creatorcontrib><creatorcontrib>Lu, Yun-Xin</creatorcontrib><creatorcontrib>Wu, Qi-Nian</creatorcontrib><creatorcontrib>Pu, Heng-Ying</creatorcontrib><creatorcontrib>Zeng, Zhao-Lei</creatorcontrib><creatorcontrib>Xie, Dan</creatorcontrib><creatorcontrib>Ju, Huai-Qiang</creatorcontrib><creatorcontrib>Luo, Hui-Yan</creatorcontrib><creatorcontrib>Xu, Rui-Hua</creatorcontrib><title>VDR–SOX2 signaling promotes colorectal cancer stemness and malignancy in an acidic microenvironment</title><title>Signal transduction and targeted therapy</title><addtitle>Sig Transduct Target Ther</addtitle><addtitle>Signal Transduct Target Ther</addtitle><description>The acidic tumor microenvironment provides an energy source driving malignant tumor progression. Adaptation of cells to an acidic environment leads to the emergence of cancer stem cells. The expression of the vitamin D receptor (VDR) is closely related to the initiation and development of colorectal carcinoma (CRC), but its regulatory mechanism in CRC stem cells is still unclear. Our study revealed that acidosis reduced VDR expression by downregulating peroxisome proliferator-activated receptor delta (PPARD) expression. Overexpression of VDR effectively suppressed the stemness and oxaliplatin resistance of cells in acidosis. The nuclear export signal in VDR was sensitive to acidosis, and VDR was exported from the nucleus. Chromatin immunoprecipitation (ChIP) and assay for transposase-accessible chromatin with high-throughput sequencing (ATAC-seq) analyses showed that VDR transcriptionally repressed SRY-box 2 (
SOX2
) by binding to the vitamin D response elements in the promoter of
SOX2
, impairing tumor growth and drug resistance. We demonstrated that a change in the acidic microenvironment combined with overexpression of VDR substantially restricted the occurrence and development of CRC in vivo. These findings reveal a new mechanism by which acidosis could affect the stemness of CRC cells by regulating the expression of SOX2 and show that abnormal VDR expression leads to ineffective activation of vitamin D signaling, resulting in a lack of efficacy of vitamin D in antineoplastic process.</description><subject>631/337/176</subject><subject>631/532/71</subject><subject>631/67/1504</subject><subject>Acidosis</subject><subject>Cancer Research</subject><subject>Cell Biology</subject><subject>Colorectal cancer</subject><subject>Internal Medicine</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Oncology</subject><subject>Pathology</subject><subject>Stem cells</subject><subject>Vitamin 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transduction and targeted therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Pei-Shan</au><au>Li, Ting</au><au>Lin, Jin-Fei</au><au>Qiu, Miao-Zhen</au><au>Wang, De-Shen</au><au>Liu, Ze-Xian</au><au>Chen, Zhan-Hong</au><au>Yang, Lu-Ping</au><au>Zhang, Xiao-Long</au><au>Zhao, Qi</au><au>Chen, Yan-Xing</au><au>Lu, Yun-Xin</au><au>Wu, Qi-Nian</au><au>Pu, Heng-Ying</au><au>Zeng, Zhao-Lei</au><au>Xie, Dan</au><au>Ju, Huai-Qiang</au><au>Luo, Hui-Yan</au><au>Xu, Rui-Hua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>VDR–SOX2 signaling promotes colorectal cancer stemness and malignancy in an acidic microenvironment</atitle><jtitle>Signal transduction and targeted therapy</jtitle><stitle>Sig Transduct Target Ther</stitle><addtitle>Signal Transduct Target Ther</addtitle><date>2020-09-09</date><risdate>2020</risdate><volume>5</volume><issue>1</issue><spage>183</spage><epage>183</epage><pages>183-183</pages><artnum>183</artnum><issn>2059-3635</issn><issn>2095-9907</issn><eissn>2059-3635</eissn><abstract>The acidic tumor microenvironment provides an energy source driving malignant tumor progression. Adaptation of cells to an acidic environment leads to the emergence of cancer stem cells. The expression of the vitamin D receptor (VDR) is closely related to the initiation and development of colorectal carcinoma (CRC), but its regulatory mechanism in CRC stem cells is still unclear. Our study revealed that acidosis reduced VDR expression by downregulating peroxisome proliferator-activated receptor delta (PPARD) expression. Overexpression of VDR effectively suppressed the stemness and oxaliplatin resistance of cells in acidosis. The nuclear export signal in VDR was sensitive to acidosis, and VDR was exported from the nucleus. Chromatin immunoprecipitation (ChIP) and assay for transposase-accessible chromatin with high-throughput sequencing (ATAC-seq) analyses showed that VDR transcriptionally repressed SRY-box 2 (
SOX2
) by binding to the vitamin D response elements in the promoter of
SOX2
, impairing tumor growth and drug resistance. We demonstrated that a change in the acidic microenvironment combined with overexpression of VDR substantially restricted the occurrence and development of CRC in vivo. These findings reveal a new mechanism by which acidosis could affect the stemness of CRC cells by regulating the expression of SOX2 and show that abnormal VDR expression leads to ineffective activation of vitamin D signaling, resulting in a lack of efficacy of vitamin D in antineoplastic process.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>32900990</pmid><doi>10.1038/s41392-020-00230-7</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-2242-3138</orcidid><orcidid>https://orcid.org/0000-0003-1713-5465</orcidid><orcidid>https://orcid.org/0000-0001-9771-8534</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/337/176 631/532/71 631/67/1504 Acidosis Cancer Research Cell Biology Colorectal cancer Internal Medicine Medicine Medicine & Public Health Oncology Pathology Stem cells Vitamin D |
title | VDR–SOX2 signaling promotes colorectal cancer stemness and malignancy in an acidic microenvironment |
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