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Circ_0060731 mediated miR-21–5p-PDCD4/ESR1 pathway to induce apoptosis of placental trophoblasts in intrahepatic cholestasis of pregnancy

Intrahepatic cholestasis of pregnancy (ICP) is a pregnancy complication. However, the pathogenesis of ICP is currently unclear. We analyzed the placenta samples of 10 normal and 10 ICP pregnant women. the expressions of circ0060731, miR-21–5p, and their downstream target genes PDCD4, ESR1, and apopt...

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Published in:Tissue & cell 2022-06, Vol.76, p.101771-101771, Article 101771
Main Authors: Feng, Fan, Lei, Lei, Liao, Junqun, Huang, Xiaomei, Shao, Yong
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Lei, Lei
Liao, Junqun
Huang, Xiaomei
Shao, Yong
description Intrahepatic cholestasis of pregnancy (ICP) is a pregnancy complication. However, the pathogenesis of ICP is currently unclear. We analyzed the placenta samples of 10 normal and 10 ICP pregnant women. the expressions of circ0060731, miR-21–5p, and their downstream target genes PDCD4, ESR1, and apoptotic protein cleaved-caspase3 were detected in the cell model. The expression of Circ_0060731, PDCD4, ESR1, and caspase-3 was higher in the ICP placenta tissue than in the control group, and the expression of miR-21–5p was lower in the ICP group than in the control group. In HTR8/Svneo cells treated with TCA, the expression/levels of Circ_0060731, PDCD4, ESR1, and caspase-3 were significantly higher in the ICP group than in the control group, and miR-21–5p was significantly lower in the ICP group than in the control group. Lentiviral knockdown of miR-21–5p significantly increased the expressions of its downstream genes of PDCD4 and ESR1, and also increased cell apoptosis. Overexpression of miR-21–5p significantly reduced the expression of PDCD4 and ESR1 and reduced cell apoptosis. The dual-luciferase experiment showed that both PDCD4 and ERS1 were the target genes of miR-21–5p. Circ_0060731 mediated miR-21–5p-PDCD4/ESR1 pathway could induce apoptosis of placental trophoblasts in intrahepatic cholestasis of pregnancy. •Expression of miR-21–5p was lower in placenta of intrahepatic cholestasis of pregnancy.•Expression of circ_0060731 was higher in placenta of intrahepatic cholestasis of pregnancy.•PDCD and ESR1 are target genes of miR-21–5p.•Circ0060731 may mediate placental trophoblast apoptosis by regulating miR-21–5p-PDCD4 / ESR1 pathway.
doi_str_mv 10.1016/j.tice.2022.101771
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However, the pathogenesis of ICP is currently unclear. We analyzed the placenta samples of 10 normal and 10 ICP pregnant women. the expressions of circ0060731, miR-21–5p, and their downstream target genes PDCD4, ESR1, and apoptotic protein cleaved-caspase3 were detected in the cell model. The expression of Circ_0060731, PDCD4, ESR1, and caspase-3 was higher in the ICP placenta tissue than in the control group, and the expression of miR-21–5p was lower in the ICP group than in the control group. In HTR8/Svneo cells treated with TCA, the expression/levels of Circ_0060731, PDCD4, ESR1, and caspase-3 were significantly higher in the ICP group than in the control group, and miR-21–5p was significantly lower in the ICP group than in the control group. Lentiviral knockdown of miR-21–5p significantly increased the expressions of its downstream genes of PDCD4 and ESR1, and also increased cell apoptosis. Overexpression of miR-21–5p significantly reduced the expression of PDCD4 and ESR1 and reduced cell apoptosis. The dual-luciferase experiment showed that both PDCD4 and ERS1 were the target genes of miR-21–5p. Circ_0060731 mediated miR-21–5p-PDCD4/ESR1 pathway could induce apoptosis of placental trophoblasts in intrahepatic cholestasis of pregnancy. •Expression of miR-21–5p was lower in placenta of intrahepatic cholestasis of pregnancy.•Expression of circ_0060731 was higher in placenta of intrahepatic cholestasis of pregnancy.•PDCD and ESR1 are target genes of miR-21–5p.•Circ0060731 may mediate placental trophoblast apoptosis by regulating miR-21–5p-PDCD4 / ESR1 pathway.</description><identifier>ISSN: 0040-8166</identifier><identifier>EISSN: 1532-3072</identifier><identifier>DOI: 10.1016/j.tice.2022.101771</identifier><identifier>PMID: 35279605</identifier><language>eng</language><publisher>Scotland: Elsevier Ltd</publisher><subject>Apoptosis ; Caspase-3 ; Cholestasis ; Chromosome 5 ; Circ_0060731 ; ESR1 protein ; Gallbladder diseases ; Genes ; Intrahepatic cholestasis of pregnancy ; MiR-21–5p ; Pathogenesis ; Placenta ; Pregnancy ; Pregnancy complications ; Trophoblasts</subject><ispartof>Tissue &amp; cell, 2022-06, Vol.76, p.101771-101771, Article 101771</ispartof><rights>2022 Elsevier Ltd</rights><rights>Copyright © 2022 Elsevier Ltd. 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However, the pathogenesis of ICP is currently unclear. We analyzed the placenta samples of 10 normal and 10 ICP pregnant women. the expressions of circ0060731, miR-21–5p, and their downstream target genes PDCD4, ESR1, and apoptotic protein cleaved-caspase3 were detected in the cell model. The expression of Circ_0060731, PDCD4, ESR1, and caspase-3 was higher in the ICP placenta tissue than in the control group, and the expression of miR-21–5p was lower in the ICP group than in the control group. In HTR8/Svneo cells treated with TCA, the expression/levels of Circ_0060731, PDCD4, ESR1, and caspase-3 were significantly higher in the ICP group than in the control group, and miR-21–5p was significantly lower in the ICP group than in the control group. Lentiviral knockdown of miR-21–5p significantly increased the expressions of its downstream genes of PDCD4 and ESR1, and also increased cell apoptosis. 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Circ_0060731 mediated miR-21–5p-PDCD4/ESR1 pathway could induce apoptosis of placental trophoblasts in intrahepatic cholestasis of pregnancy. •Expression of miR-21–5p was lower in placenta of intrahepatic cholestasis of pregnancy.•Expression of circ_0060731 was higher in placenta of intrahepatic cholestasis of pregnancy.•PDCD and ESR1 are target genes of miR-21–5p.•Circ0060731 may mediate placental trophoblast apoptosis by regulating miR-21–5p-PDCD4 / ESR1 pathway.</description><subject>Apoptosis</subject><subject>Caspase-3</subject><subject>Cholestasis</subject><subject>Chromosome 5</subject><subject>Circ_0060731</subject><subject>ESR1 protein</subject><subject>Gallbladder diseases</subject><subject>Genes</subject><subject>Intrahepatic cholestasis of pregnancy</subject><subject>MiR-21–5p</subject><subject>Pathogenesis</subject><subject>Placenta</subject><subject>Pregnancy</subject><subject>Pregnancy complications</subject><subject>Trophoblasts</subject><issn>0040-8166</issn><issn>1532-3072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kc2KFDEURoMoTs_oC7iQgBs31XOTVH4G3EjPjAoDyqjrkE7dstNUV8okpfTOvUvf0CcxTc-4cCGEBML5LpfvEPKMwZIBU-fbZQkelxw4P3xozR6QBZOCNwI0f0gWAC00hil1Qk5z3gKAbpl-TE6E5PpCgVyQn6uQvAVQoAWjO-yCK9jRXbhtOPv945ecmg-Xq8v2_OrjLaOTK5vvbk9LpGHsZo_UTXEqMYdMY0-nwXkcixtoSXHaxPXgcskVrackt8GaD576TRwwF3efSvhldKPfPyGPejdkfHr3npHP11efVm-bm_dv3q1e3zRemLY0yBUXXvTQMQYXTEvRM6OEVPVi3KM3HRrJvO7bVsJaSSdlx0H3Grpe9lyckZfHuVOKX-e6id2F7HEY3IhxzpYrYWo7hpmKvvgH3cY5jXW7ShlthJC6rRQ_Uj7FnBP2dkph59LeMrAHVXZrD6rsQZU9qqqh53ej53Xt_W_k3k0FXh0BrF18C5hs9gFHXx0l9MV2Mfxv_h-g_KOs</recordid><startdate>20220601</startdate><enddate>20220601</enddate><creator>Feng, Fan</creator><creator>Lei, Lei</creator><creator>Liao, Junqun</creator><creator>Huang, Xiaomei</creator><creator>Shao, Yong</creator><general>Elsevier Ltd</general><general>Elsevier Science Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20220601</creationdate><title>Circ_0060731 mediated miR-21–5p-PDCD4/ESR1 pathway to induce apoptosis of placental trophoblasts in intrahepatic cholestasis of pregnancy</title><author>Feng, Fan ; Lei, Lei ; Liao, Junqun ; Huang, Xiaomei ; Shao, Yong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-e2623c3f0d11091753f18635686312cec8de851c7f4450b65a55d207f70df5f23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Apoptosis</topic><topic>Caspase-3</topic><topic>Cholestasis</topic><topic>Chromosome 5</topic><topic>Circ_0060731</topic><topic>ESR1 protein</topic><topic>Gallbladder diseases</topic><topic>Genes</topic><topic>Intrahepatic cholestasis of pregnancy</topic><topic>MiR-21–5p</topic><topic>Pathogenesis</topic><topic>Placenta</topic><topic>Pregnancy</topic><topic>Pregnancy complications</topic><topic>Trophoblasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Feng, Fan</creatorcontrib><creatorcontrib>Lei, Lei</creatorcontrib><creatorcontrib>Liao, Junqun</creatorcontrib><creatorcontrib>Huang, Xiaomei</creatorcontrib><creatorcontrib>Shao, Yong</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Tissue &amp; cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feng, Fan</au><au>Lei, Lei</au><au>Liao, Junqun</au><au>Huang, Xiaomei</au><au>Shao, Yong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Circ_0060731 mediated miR-21–5p-PDCD4/ESR1 pathway to induce apoptosis of placental trophoblasts in intrahepatic cholestasis of pregnancy</atitle><jtitle>Tissue &amp; cell</jtitle><addtitle>Tissue Cell</addtitle><date>2022-06-01</date><risdate>2022</risdate><volume>76</volume><spage>101771</spage><epage>101771</epage><pages>101771-101771</pages><artnum>101771</artnum><issn>0040-8166</issn><eissn>1532-3072</eissn><abstract>Intrahepatic cholestasis of pregnancy (ICP) is a pregnancy complication. 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Overexpression of miR-21–5p significantly reduced the expression of PDCD4 and ESR1 and reduced cell apoptosis. The dual-luciferase experiment showed that both PDCD4 and ERS1 were the target genes of miR-21–5p. Circ_0060731 mediated miR-21–5p-PDCD4/ESR1 pathway could induce apoptosis of placental trophoblasts in intrahepatic cholestasis of pregnancy. •Expression of miR-21–5p was lower in placenta of intrahepatic cholestasis of pregnancy.•Expression of circ_0060731 was higher in placenta of intrahepatic cholestasis of pregnancy.•PDCD and ESR1 are target genes of miR-21–5p.•Circ0060731 may mediate placental trophoblast apoptosis by regulating miR-21–5p-PDCD4 / ESR1 pathway.</abstract><cop>Scotland</cop><pub>Elsevier Ltd</pub><pmid>35279605</pmid><doi>10.1016/j.tice.2022.101771</doi><tpages>1</tpages></addata></record>
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subjects Apoptosis
Caspase-3
Cholestasis
Chromosome 5
Circ_0060731
ESR1 protein
Gallbladder diseases
Genes
Intrahepatic cholestasis of pregnancy
MiR-21–5p
Pathogenesis
Placenta
Pregnancy
Pregnancy complications
Trophoblasts
title Circ_0060731 mediated miR-21–5p-PDCD4/ESR1 pathway to induce apoptosis of placental trophoblasts in intrahepatic cholestasis of pregnancy
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