Toxic Effects of Tetrabromobisphenol A on Human Hepatocellular Carcinoma Cells(HepG2) Evaluated Using RNA-Seq
Tetrabromobisphenol A(TBBPA) is used as a brominated flame retardant and can easily release into environment. It has been detected in a variety of environmental media and even in food, making it a new pollutant that is potentially harmful to environment and human health. However, the toxicity and un...
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Veröffentlicht in: | Chemical research in Chinese universities 2023-06, Vol.39 (3), p.395-398 |
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description | Tetrabromobisphenol A(TBBPA) is used as a brominated flame retardant and can easily release into environment. It has been detected in a variety of environmental media and even in food, making it a new pollutant that is potentially harmful to environment and human health. However, the toxicity and underlying mechanism of TBBPA remain to be explored. TBBPA is actively metabolized in the liver, so it is vital to study the hepatocellular toxicity of TBBPA. In this study, we treated hepatocellular carcinoma cells(HepG2) with TBBPA and searched the differentially expressed genes(DEGs) triggered by TBBPA exposure. RNA-seq analysis showed that the expression of genes, such as
CLIC1
and
GATSL1
, were significantly down-regulated and
PTENP1
was significantly up-regulated after TBBPA exposure, and these genes were involved in cell proliferation and metabolism. The down-regulated genes were enriched to peroxisome proliferator-activated receptor(PPAR) signaling pathway and up-regulated genes were enriched to Janus Kinase-signal transduces and activators of transcription(JAK-STAT) signaling pathway, which play a role in regulating cell growth. Overall, our transcriptome analysis obtained for TBBPA-treated HepG2 cells implies that TBBPA affects the cell proliferation and growth. |
doi_str_mv | 10.1007/s40242-023-3069-2 |
format | Article |
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CLIC1
and
GATSL1
, were significantly down-regulated and
PTENP1
was significantly up-regulated after TBBPA exposure, and these genes were involved in cell proliferation and metabolism. The down-regulated genes were enriched to peroxisome proliferator-activated receptor(PPAR) signaling pathway and up-regulated genes were enriched to Janus Kinase-signal transduces and activators of transcription(JAK-STAT) signaling pathway, which play a role in regulating cell growth. Overall, our transcriptome analysis obtained for TBBPA-treated HepG2 cells implies that TBBPA affects the cell proliferation and growth.</description><identifier>ISSN: 1005-9040</identifier><identifier>EISSN: 2210-3171</identifier><identifier>DOI: 10.1007/s40242-023-3069-2</identifier><language>eng</language><publisher>Changchun: Jilin University and The Editorial Department of Chemical Research in Chinese Universities</publisher><subject>Analytical Chemistry ; Bromination ; Cell growth ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Flame retardants ; Gene expression ; Genes ; Inorganic Chemistry ; Kinases ; Liver cancer ; Organic Chemistry ; Physical Chemistry ; Ribonucleic acid ; RNA ; Signaling ; Tetrabromobisphenol A ; Toxicity</subject><ispartof>Chemical research in Chinese universities, 2023-06, Vol.39 (3), p.395-398</ispartof><rights>Jilin University, The Editorial Department of Chemical Research in Chinese Universities and Springer-Verlag GmbH 2023</rights><rights>Jilin University, The Editorial Department of Chemical Research in Chinese Universities and Springer-Verlag GmbH 2023.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-ab15ba0eaab06a5bb2b4ac74a731451890014225f69416c83fbd4baf9e8cea373</citedby><cites>FETCH-LOGICAL-c316t-ab15ba0eaab06a5bb2b4ac74a731451890014225f69416c83fbd4baf9e8cea373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s40242-023-3069-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s40242-023-3069-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Chang, Haoran</creatorcontrib><creatorcontrib>Ding, Qingjiang</creatorcontrib><creatorcontrib>Wang, Hailin</creatorcontrib><title>Toxic Effects of Tetrabromobisphenol A on Human Hepatocellular Carcinoma Cells(HepG2) Evaluated Using RNA-Seq</title><title>Chemical research in Chinese universities</title><addtitle>Chem. Res. Chin. Univ</addtitle><description>Tetrabromobisphenol A(TBBPA) is used as a brominated flame retardant and can easily release into environment. It has been detected in a variety of environmental media and even in food, making it a new pollutant that is potentially harmful to environment and human health. However, the toxicity and underlying mechanism of TBBPA remain to be explored. TBBPA is actively metabolized in the liver, so it is vital to study the hepatocellular toxicity of TBBPA. In this study, we treated hepatocellular carcinoma cells(HepG2) with TBBPA and searched the differentially expressed genes(DEGs) triggered by TBBPA exposure. RNA-seq analysis showed that the expression of genes, such as
CLIC1
and
GATSL1
, were significantly down-regulated and
PTENP1
was significantly up-regulated after TBBPA exposure, and these genes were involved in cell proliferation and metabolism. The down-regulated genes were enriched to peroxisome proliferator-activated receptor(PPAR) signaling pathway and up-regulated genes were enriched to Janus Kinase-signal transduces and activators of transcription(JAK-STAT) signaling pathway, which play a role in regulating cell growth. Overall, our transcriptome analysis obtained for TBBPA-treated HepG2 cells implies that TBBPA affects the cell proliferation and growth.</description><subject>Analytical Chemistry</subject><subject>Bromination</subject><subject>Cell growth</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Flame retardants</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Inorganic Chemistry</subject><subject>Kinases</subject><subject>Liver cancer</subject><subject>Organic Chemistry</subject><subject>Physical Chemistry</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Signaling</subject><subject>Tetrabromobisphenol A</subject><subject>Toxicity</subject><issn>1005-9040</issn><issn>2210-3171</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LAzEQhoMoWKs_wFvAix6i-dqvYym1FURB23OYpNm6ZXezTXZF_70pK3jyMgMzzzsDD0LXjN4zSrOHICmXnFAuiKBpQfgJmnDOKBEsY6doEqGEFFTSc3QRwp5SUaSpnKBm7b4qgxdlaU0fsCvx2vYetHeN01XoPmzrajzDrsWroYFYbQe9M7auhxo8noM3VesawPM4CrdxveR3ePEJ9QC93eJNqNodfnuZkXd7uERnJdTBXv32Kdo8LtbzFXl-XT7NZ8_ECJb2BDRLNFALoGkKidZcSzCZhEwwmbC8oJRJzpMyLSRLTS5KvZUaysLmxoLIxBTdjHc77w6DDb3au8G38aXiOZeyyATPI8VGyngXgrel6nzVgP9WjKqjVTVaVdGqOlpVPGb4mAmRbXfW_13-P_QDItd5yQ</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Chang, Haoran</creator><creator>Ding, Qingjiang</creator><creator>Wang, Hailin</creator><general>Jilin University and The Editorial Department of Chemical Research in Chinese Universities</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20230601</creationdate><title>Toxic Effects of Tetrabromobisphenol A on Human Hepatocellular Carcinoma Cells(HepG2) Evaluated Using RNA-Seq</title><author>Chang, Haoran ; Ding, Qingjiang ; Wang, Hailin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-ab15ba0eaab06a5bb2b4ac74a731451890014225f69416c83fbd4baf9e8cea373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Analytical Chemistry</topic><topic>Bromination</topic><topic>Cell growth</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Flame retardants</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Inorganic Chemistry</topic><topic>Kinases</topic><topic>Liver cancer</topic><topic>Organic Chemistry</topic><topic>Physical Chemistry</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Signaling</topic><topic>Tetrabromobisphenol A</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chang, Haoran</creatorcontrib><creatorcontrib>Ding, Qingjiang</creatorcontrib><creatorcontrib>Wang, Hailin</creatorcontrib><collection>CrossRef</collection><jtitle>Chemical research in Chinese universities</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chang, Haoran</au><au>Ding, Qingjiang</au><au>Wang, Hailin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Toxic Effects of Tetrabromobisphenol A on Human Hepatocellular Carcinoma Cells(HepG2) Evaluated Using RNA-Seq</atitle><jtitle>Chemical research in Chinese universities</jtitle><stitle>Chem. Res. Chin. Univ</stitle><date>2023-06-01</date><risdate>2023</risdate><volume>39</volume><issue>3</issue><spage>395</spage><epage>398</epage><pages>395-398</pages><issn>1005-9040</issn><eissn>2210-3171</eissn><abstract>Tetrabromobisphenol A(TBBPA) is used as a brominated flame retardant and can easily release into environment. It has been detected in a variety of environmental media and even in food, making it a new pollutant that is potentially harmful to environment and human health. However, the toxicity and underlying mechanism of TBBPA remain to be explored. TBBPA is actively metabolized in the liver, so it is vital to study the hepatocellular toxicity of TBBPA. In this study, we treated hepatocellular carcinoma cells(HepG2) with TBBPA and searched the differentially expressed genes(DEGs) triggered by TBBPA exposure. RNA-seq analysis showed that the expression of genes, such as
CLIC1
and
GATSL1
, were significantly down-regulated and
PTENP1
was significantly up-regulated after TBBPA exposure, and these genes were involved in cell proliferation and metabolism. The down-regulated genes were enriched to peroxisome proliferator-activated receptor(PPAR) signaling pathway and up-regulated genes were enriched to Janus Kinase-signal transduces and activators of transcription(JAK-STAT) signaling pathway, which play a role in regulating cell growth. Overall, our transcriptome analysis obtained for TBBPA-treated HepG2 cells implies that TBBPA affects the cell proliferation and growth.</abstract><cop>Changchun</cop><pub>Jilin University and The Editorial Department of Chemical Research in Chinese Universities</pub><doi>10.1007/s40242-023-3069-2</doi><tpages>4</tpages></addata></record> |
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subjects | Analytical Chemistry Bromination Cell growth Chemistry Chemistry and Materials Science Chemistry/Food Science Flame retardants Gene expression Genes Inorganic Chemistry Kinases Liver cancer Organic Chemistry Physical Chemistry Ribonucleic acid RNA Signaling Tetrabromobisphenol A Toxicity |
title | Toxic Effects of Tetrabromobisphenol A on Human Hepatocellular Carcinoma Cells(HepG2) Evaluated Using RNA-Seq |
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