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Estrogen receptor-related receptor γ uppresses hypoxia-induced angiogenesis by regulating VEGFA in endometrial cancer

OBJECTIVEEstrogen receptor-related receptor γ (ERRγ), is implicated in cancer cell proliferation and metastasis. The function of ERRγ in tumor angiogenesis, however, is to be revealed. This study was designed to elaborate the regulatory effect of ERRγ on angiogenesis in endometrial cancer (EC).METHO...

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Published in:Gynecological endocrinology 2023-12, Vol.39 (1), p.2264411-2264411
Main Authors: Wang, Xiao-xiao, Hua, Teng, Wang, Hong-bo
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Hua, Teng
Wang, Hong-bo
description OBJECTIVEEstrogen receptor-related receptor γ (ERRγ), is implicated in cancer cell proliferation and metastasis. The function of ERRγ in tumor angiogenesis, however, is to be revealed. This study was designed to elaborate the regulatory effect of ERRγ on angiogenesis in endometrial cancer (EC).METHODSImmunohistochemistry (IHC) was adopted to determine the protein expression of ERRγ, VEGFA, CD31 and hypoxia-inducible factor-1 (HIF-1) in tumor tissues. HEC-1A cells stably expressing ERRγ were established bytransfection, and then an endothelial cell tube formation assay was performed. CCK-8 assay was employed for cell viability, and wound healing assay for cell migration ability. Besides, western blot, ELISA and qRT-PCR were used to examine the VEGFA expression. After hypoxia treatment of ERRγ overexpressing HEC-1A cells, the ERRγ expression and VEGFA expression were determined by western blot. Finally, EC xenografts in nude mice were constructed by subcutaneous injection of ERRγ stably expressing HEC-1A cells and control HEC-1A cells.RESULTSIHC results revealed a negative correlation between the expression of ERRγ and VEGFA in EC tissues. ERRγ overexpression significantly decreased the level of HIF-1 in tumor tissue of nude mice. ERRγ overexpression down-regulated inhibited angiogenesis capability and inhibited the proliferation and migration of HEC-1A cells. Furthermore, ERRγ expression was suppressed under the condition of hypoxia while restoration of ERRγ partially inhibited hypoxia-induced VEGFA expression in HEC-1A cells.CONCLUSIONSERRγ is an angiogenesis suppressor and involved in hypoxia-induced VEGFA expression in EC. Hence, ERRγ might be a promising antiangiogenic target for human EC.
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The function of ERRγ in tumor angiogenesis, however, is to be revealed. This study was designed to elaborate the regulatory effect of ERRγ on angiogenesis in endometrial cancer (EC).METHODSImmunohistochemistry (IHC) was adopted to determine the protein expression of ERRγ, VEGFA, CD31 and hypoxia-inducible factor-1 (HIF-1) in tumor tissues. HEC-1A cells stably expressing ERRγ were established bytransfection, and then an endothelial cell tube formation assay was performed. CCK-8 assay was employed for cell viability, and wound healing assay for cell migration ability. Besides, western blot, ELISA and qRT-PCR were used to examine the VEGFA expression. After hypoxia treatment of ERRγ overexpressing HEC-1A cells, the ERRγ expression and VEGFA expression were determined by western blot. Finally, EC xenografts in nude mice were constructed by subcutaneous injection of ERRγ stably expressing HEC-1A cells and control HEC-1A cells.RESULTSIHC results revealed a negative correlation between the expression of ERRγ and VEGFA in EC tissues. ERRγ overexpression significantly decreased the level of HIF-1 in tumor tissue of nude mice. ERRγ overexpression down-regulated inhibited angiogenesis capability and inhibited the proliferation and migration of HEC-1A cells. Furthermore, ERRγ expression was suppressed under the condition of hypoxia while restoration of ERRγ partially inhibited hypoxia-induced VEGFA expression in HEC-1A cells.CONCLUSIONSERRγ is an angiogenesis suppressor and involved in hypoxia-induced VEGFA expression in EC. Hence, ERRγ might be a promising antiangiogenic target for human EC.</description><identifier>ISSN: 0951-3590</identifier><identifier>EISSN: 1473-0766</identifier><identifier>DOI: 10.1080/09513590.2023.2264411</identifier><language>eng</language><publisher>Taylor &amp; Francis Group</publisher><subject>angiogenesis ; Endometrial cancer (EC) ; estrogen receptor-related receptor γ (ERRγ) ; hypoxia ; vascular endothelial growth factor A (VEGFA)</subject><ispartof>Gynecological endocrinology, 2023-12, Vol.39 (1), p.2264411-2264411</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-9b71104d43d3c373c61d58997f6e3e187fef3b01dd43a7b35cebeb43588d8c633</citedby><cites>FETCH-LOGICAL-c399t-9b71104d43d3c373c61d58997f6e3e187fef3b01dd43a7b35cebeb43588d8c633</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Wang, Xiao-xiao</creatorcontrib><creatorcontrib>Hua, Teng</creatorcontrib><creatorcontrib>Wang, Hong-bo</creatorcontrib><title>Estrogen receptor-related receptor γ uppresses hypoxia-induced angiogenesis by regulating VEGFA in endometrial cancer</title><title>Gynecological endocrinology</title><description>OBJECTIVEEstrogen receptor-related receptor γ (ERRγ), is implicated in cancer cell proliferation and metastasis. The function of ERRγ in tumor angiogenesis, however, is to be revealed. This study was designed to elaborate the regulatory effect of ERRγ on angiogenesis in endometrial cancer (EC).METHODSImmunohistochemistry (IHC) was adopted to determine the protein expression of ERRγ, VEGFA, CD31 and hypoxia-inducible factor-1 (HIF-1) in tumor tissues. HEC-1A cells stably expressing ERRγ were established bytransfection, and then an endothelial cell tube formation assay was performed. CCK-8 assay was employed for cell viability, and wound healing assay for cell migration ability. Besides, western blot, ELISA and qRT-PCR were used to examine the VEGFA expression. After hypoxia treatment of ERRγ overexpressing HEC-1A cells, the ERRγ expression and VEGFA expression were determined by western blot. Finally, EC xenografts in nude mice were constructed by subcutaneous injection of ERRγ stably expressing HEC-1A cells and control HEC-1A cells.RESULTSIHC results revealed a negative correlation between the expression of ERRγ and VEGFA in EC tissues. ERRγ overexpression significantly decreased the level of HIF-1 in tumor tissue of nude mice. ERRγ overexpression down-regulated inhibited angiogenesis capability and inhibited the proliferation and migration of HEC-1A cells. Furthermore, ERRγ expression was suppressed under the condition of hypoxia while restoration of ERRγ partially inhibited hypoxia-induced VEGFA expression in HEC-1A cells.CONCLUSIONSERRγ is an angiogenesis suppressor and involved in hypoxia-induced VEGFA expression in EC. Hence, ERRγ might be a promising antiangiogenic target for human EC.</description><subject>angiogenesis</subject><subject>Endometrial cancer (EC)</subject><subject>estrogen receptor-related receptor γ (ERRγ)</subject><subject>hypoxia</subject><subject>vascular endothelial growth factor A (VEGFA)</subject><issn>0951-3590</issn><issn>1473-0766</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNo9kcFq3DAQhkVpINtNHiGgYy_eSpZkScew7G4DgVySXoUsjR0Fr-VKduk-V98jz1S7m-5pYPj-f2A-hO4o2VCiyDeiBWVCk01JSrYpy4pzSj-hFeWSFURW1We0Wphiga7Rl5zfCKGMy3KFfu3ymGILPU7gYBhjKhJ0dgR_WeD3P3gahgQ5Q8avpyH-DrYIvZ_cTNm-DUsecsi4Ps2pdprzoW_xj91hf49Dj6H38QhjCrbDzvYO0g26amyX4fZjrtHLfve8_V48Ph0etvePhWNaj4WuJaWEe848c0wyV1EvlNayqYABVbKBhtWE-pmwsmbCQQ01Z0Ipr1zF2Bo9nHt9tG9mSOFo08lEG8y_RUytsWkMrgPjwVML889UqbnlYKEmQoDzlpdCSj13fT13DSn-nCCP5hiyg66zPcQpm1IpQrTms4Q1EmfUpZhzguZymhKzODP_nZnFmflwxv4C-RCMZQ</recordid><startdate>20231214</startdate><enddate>20231214</enddate><creator>Wang, Xiao-xiao</creator><creator>Hua, Teng</creator><creator>Wang, Hong-bo</creator><general>Taylor &amp; Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>20231214</creationdate><title>Estrogen receptor-related receptor γ uppresses hypoxia-induced angiogenesis by regulating VEGFA in endometrial cancer</title><author>Wang, Xiao-xiao ; Hua, Teng ; Wang, Hong-bo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-9b71104d43d3c373c61d58997f6e3e187fef3b01dd43a7b35cebeb43588d8c633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>angiogenesis</topic><topic>Endometrial cancer (EC)</topic><topic>estrogen receptor-related receptor γ (ERRγ)</topic><topic>hypoxia</topic><topic>vascular endothelial growth factor A (VEGFA)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Xiao-xiao</creatorcontrib><creatorcontrib>Hua, Teng</creatorcontrib><creatorcontrib>Wang, Hong-bo</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Gynecological endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Xiao-xiao</au><au>Hua, Teng</au><au>Wang, Hong-bo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Estrogen receptor-related receptor γ uppresses hypoxia-induced angiogenesis by regulating VEGFA in endometrial cancer</atitle><jtitle>Gynecological endocrinology</jtitle><date>2023-12-14</date><risdate>2023</risdate><volume>39</volume><issue>1</issue><spage>2264411</spage><epage>2264411</epage><pages>2264411-2264411</pages><issn>0951-3590</issn><eissn>1473-0766</eissn><abstract>OBJECTIVEEstrogen receptor-related receptor γ (ERRγ), is implicated in cancer cell proliferation and metastasis. The function of ERRγ in tumor angiogenesis, however, is to be revealed. This study was designed to elaborate the regulatory effect of ERRγ on angiogenesis in endometrial cancer (EC).METHODSImmunohistochemistry (IHC) was adopted to determine the protein expression of ERRγ, VEGFA, CD31 and hypoxia-inducible factor-1 (HIF-1) in tumor tissues. HEC-1A cells stably expressing ERRγ were established bytransfection, and then an endothelial cell tube formation assay was performed. CCK-8 assay was employed for cell viability, and wound healing assay for cell migration ability. Besides, western blot, ELISA and qRT-PCR were used to examine the VEGFA expression. After hypoxia treatment of ERRγ overexpressing HEC-1A cells, the ERRγ expression and VEGFA expression were determined by western blot. Finally, EC xenografts in nude mice were constructed by subcutaneous injection of ERRγ stably expressing HEC-1A cells and control HEC-1A cells.RESULTSIHC results revealed a negative correlation between the expression of ERRγ and VEGFA in EC tissues. ERRγ overexpression significantly decreased the level of HIF-1 in tumor tissue of nude mice. ERRγ overexpression down-regulated inhibited angiogenesis capability and inhibited the proliferation and migration of HEC-1A cells. Furthermore, ERRγ expression was suppressed under the condition of hypoxia while restoration of ERRγ partially inhibited hypoxia-induced VEGFA expression in HEC-1A cells.CONCLUSIONSERRγ is an angiogenesis suppressor and involved in hypoxia-induced VEGFA expression in EC. Hence, ERRγ might be a promising antiangiogenic target for human EC.</abstract><pub>Taylor &amp; Francis Group</pub><doi>10.1080/09513590.2023.2264411</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects angiogenesis
Endometrial cancer (EC)
estrogen receptor-related receptor γ (ERRγ)
hypoxia
vascular endothelial growth factor A (VEGFA)
title Estrogen receptor-related receptor γ uppresses hypoxia-induced angiogenesis by regulating VEGFA in endometrial cancer
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