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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
Main Authors: 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
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cited_by cdi_FETCH-LOGICAL-c474t-547da14a082e87d4580eefefbcbd351e0132f246d67a7e2e999926df81d073f63
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container_title Signal transduction and targeted therapy
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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
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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. 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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. 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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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