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Synthetic retinoid CD437 induces mitochondria-mediated apoptosis in hepatocellular carcinoma cells
Retinoids play an important role in the regulation of cell growth and death. Synthetic retinoid CD437 reportedly induces apoptosis in various cancer cell lines. However, the mechanism of inducing apoptosis in hepatocellular carcinoma (HCC) cells by this agent remains to be clarified. In this study,...
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Published in: | Biochemical and biophysical research communications 2008-06, Vol.370 (4), p.629-633 |
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creator | Gonda, Kazue Tsuchiya, Hiroyuki Sakabe, Tomohiko Akechi, Yuji Ikeda, Remina Nishio, Ren Terabayashi, Kei Ishii, Kyoko Matsumi, Yoshiaki Ashla, An Afida Okamoto, Hideharu Takubo, Kazuko Matsuoka, Saori Watanabe, Yumi Hoshikawa, Yoshiko Kurimasa, Akihiro Shiota, Goshi |
description | Retinoids play an important role in the regulation of cell growth and death. Synthetic retinoid CD437 reportedly induces apoptosis in various cancer cell lines. However, the mechanism of inducing apoptosis in hepatocellular carcinoma (HCC) cells by this agent remains to be clarified. In this study, we investigated the signaling pathway by which CD437 induces apoptosis in HCC cell lines. Apoptosis of six human HCC cell lines was induced by treatment with CD437. Caspase-3 and -9 were activated by CD437, suggesting that the apoptosis is mediated by mitochondrial pathways. Consistent with these findings, the treatment with CD437 upregulated Bax protein, downregulated Bcl-2 protein and released cytochrome
c into the cytoplasm. Moreover, rhodamine123 staining revealed mitochondrial depolarization in the cells treated with CD437. These data of the present study suggest that CD437 induces apoptosis in HCC cells via mitochondrial pathways. |
doi_str_mv | 10.1016/j.bbrc.2008.04.008 |
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c into the cytoplasm. Moreover, rhodamine123 staining revealed mitochondrial depolarization in the cells treated with CD437. These data of the present study suggest that CD437 induces apoptosis in HCC cells via mitochondrial pathways.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2008.04.008</identifier><identifier>PMID: 18406343</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Apoptosis ; bcl-2-Associated X Protein - metabolism ; Carcinoma, Hepatocellular - metabolism ; Caspase 3 - metabolism ; Caspase 9 - metabolism ; CD437 ; Cell Line, Tumor ; Cell Proliferation - drug effects ; Hepatocellular carcinoma ; Humans ; Liver Neoplasms - metabolism ; Mitochondria ; Mitochondria - drug effects ; Mitochondria - metabolism ; Proto-Oncogene Proteins c-bcl-2 - antagonists & inhibitors ; Proto-Oncogene Proteins c-bcl-2 - metabolism ; Retinoids - pharmacology ; Synthetic retinoid</subject><ispartof>Biochemical and biophysical research communications, 2008-06, Vol.370 (4), p.629-633</ispartof><rights>2008 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-8597891bc928e85cbd6b99ce4cc6aa33099b4c9a927aef0d26447f105e2766c3</citedby><cites>FETCH-LOGICAL-c451t-8597891bc928e85cbd6b99ce4cc6aa33099b4c9a927aef0d26447f105e2766c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18406343$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gonda, Kazue</creatorcontrib><creatorcontrib>Tsuchiya, Hiroyuki</creatorcontrib><creatorcontrib>Sakabe, Tomohiko</creatorcontrib><creatorcontrib>Akechi, Yuji</creatorcontrib><creatorcontrib>Ikeda, Remina</creatorcontrib><creatorcontrib>Nishio, Ren</creatorcontrib><creatorcontrib>Terabayashi, Kei</creatorcontrib><creatorcontrib>Ishii, Kyoko</creatorcontrib><creatorcontrib>Matsumi, Yoshiaki</creatorcontrib><creatorcontrib>Ashla, An Afida</creatorcontrib><creatorcontrib>Okamoto, Hideharu</creatorcontrib><creatorcontrib>Takubo, Kazuko</creatorcontrib><creatorcontrib>Matsuoka, Saori</creatorcontrib><creatorcontrib>Watanabe, Yumi</creatorcontrib><creatorcontrib>Hoshikawa, Yoshiko</creatorcontrib><creatorcontrib>Kurimasa, Akihiro</creatorcontrib><creatorcontrib>Shiota, Goshi</creatorcontrib><title>Synthetic retinoid CD437 induces mitochondria-mediated apoptosis in hepatocellular carcinoma cells</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Retinoids play an important role in the regulation of cell growth and death. Synthetic retinoid CD437 reportedly induces apoptosis in various cancer cell lines. However, the mechanism of inducing apoptosis in hepatocellular carcinoma (HCC) cells by this agent remains to be clarified. In this study, we investigated the signaling pathway by which CD437 induces apoptosis in HCC cell lines. Apoptosis of six human HCC cell lines was induced by treatment with CD437. Caspase-3 and -9 were activated by CD437, suggesting that the apoptosis is mediated by mitochondrial pathways. Consistent with these findings, the treatment with CD437 upregulated Bax protein, downregulated Bcl-2 protein and released cytochrome
c into the cytoplasm. Moreover, rhodamine123 staining revealed mitochondrial depolarization in the cells treated with CD437. These data of the present study suggest that CD437 induces apoptosis in HCC cells via mitochondrial pathways.</description><subject>Apoptosis</subject><subject>bcl-2-Associated X Protein - metabolism</subject><subject>Carcinoma, Hepatocellular - metabolism</subject><subject>Caspase 3 - metabolism</subject><subject>Caspase 9 - metabolism</subject><subject>CD437</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Hepatocellular carcinoma</subject><subject>Humans</subject><subject>Liver Neoplasms - metabolism</subject><subject>Mitochondria</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - metabolism</subject><subject>Proto-Oncogene Proteins c-bcl-2 - antagonists & inhibitors</subject><subject>Proto-Oncogene Proteins c-bcl-2 - metabolism</subject><subject>Retinoids - pharmacology</subject><subject>Synthetic retinoid</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkU9r3DAQxUVoyG7SfoEeik-92R3JsmxBL2Xzp4VAD9lDbkIez7Ja1pYr2YX99pHZhd7SyzwYfvMY3mPsM4eCA1ffDkXbBiwEQFOALJJcsTUHDbngID-wNQCoXGj-umK3MR4AOJdK37AVbySoUpZr1r6chmlPk8MspDl412Wbe1nWmRu6GSlmvZs87v3QBWfznjpnJ-oyO_px8tHFxGV7Gm2C6HicjzZkaAMmp95myyp-ZNc7e4z06aJ3bPv4sN38zJ9_P_3a_HjOUVZ8yptK143mLWrRUFNh26lWaySJqKwtS9C6laitFrWlHXRCSVnvOFQkaqWwvGNfz7Zj8H9mipPpXVwesAP5ORqleS1KBf8FBdS8qhqdQHEGMfgYA-3MGFxvw8lwMEsD5mCWBszSgAFpkqSjLxf3uU1p_Tu5RJ6A72eAUhZ_HQUT0dGAKdlAOJnOu_f83wA-lZhG</recordid><startdate>20080613</startdate><enddate>20080613</enddate><creator>Gonda, Kazue</creator><creator>Tsuchiya, Hiroyuki</creator><creator>Sakabe, Tomohiko</creator><creator>Akechi, Yuji</creator><creator>Ikeda, Remina</creator><creator>Nishio, Ren</creator><creator>Terabayashi, Kei</creator><creator>Ishii, Kyoko</creator><creator>Matsumi, Yoshiaki</creator><creator>Ashla, An Afida</creator><creator>Okamoto, Hideharu</creator><creator>Takubo, Kazuko</creator><creator>Matsuoka, Saori</creator><creator>Watanabe, Yumi</creator><creator>Hoshikawa, Yoshiko</creator><creator>Kurimasa, Akihiro</creator><creator>Shiota, Goshi</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20080613</creationdate><title>Synthetic retinoid CD437 induces mitochondria-mediated apoptosis in hepatocellular carcinoma cells</title><author>Gonda, Kazue ; Tsuchiya, Hiroyuki ; Sakabe, Tomohiko ; Akechi, Yuji ; Ikeda, Remina ; Nishio, Ren ; Terabayashi, Kei ; Ishii, Kyoko ; Matsumi, Yoshiaki ; Ashla, An Afida ; Okamoto, Hideharu ; Takubo, Kazuko ; Matsuoka, Saori ; Watanabe, Yumi ; Hoshikawa, Yoshiko ; Kurimasa, Akihiro ; Shiota, Goshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-8597891bc928e85cbd6b99ce4cc6aa33099b4c9a927aef0d26447f105e2766c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Apoptosis</topic><topic>bcl-2-Associated X Protein - metabolism</topic><topic>Carcinoma, Hepatocellular - metabolism</topic><topic>Caspase 3 - metabolism</topic><topic>Caspase 9 - metabolism</topic><topic>CD437</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>Hepatocellular carcinoma</topic><topic>Humans</topic><topic>Liver Neoplasms - metabolism</topic><topic>Mitochondria</topic><topic>Mitochondria - drug effects</topic><topic>Mitochondria - metabolism</topic><topic>Proto-Oncogene Proteins c-bcl-2 - antagonists & inhibitors</topic><topic>Proto-Oncogene Proteins c-bcl-2 - metabolism</topic><topic>Retinoids - pharmacology</topic><topic>Synthetic retinoid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gonda, Kazue</creatorcontrib><creatorcontrib>Tsuchiya, Hiroyuki</creatorcontrib><creatorcontrib>Sakabe, Tomohiko</creatorcontrib><creatorcontrib>Akechi, Yuji</creatorcontrib><creatorcontrib>Ikeda, Remina</creatorcontrib><creatorcontrib>Nishio, Ren</creatorcontrib><creatorcontrib>Terabayashi, Kei</creatorcontrib><creatorcontrib>Ishii, Kyoko</creatorcontrib><creatorcontrib>Matsumi, Yoshiaki</creatorcontrib><creatorcontrib>Ashla, An Afida</creatorcontrib><creatorcontrib>Okamoto, Hideharu</creatorcontrib><creatorcontrib>Takubo, Kazuko</creatorcontrib><creatorcontrib>Matsuoka, Saori</creatorcontrib><creatorcontrib>Watanabe, Yumi</creatorcontrib><creatorcontrib>Hoshikawa, Yoshiko</creatorcontrib><creatorcontrib>Kurimasa, Akihiro</creatorcontrib><creatorcontrib>Shiota, Goshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gonda, Kazue</au><au>Tsuchiya, Hiroyuki</au><au>Sakabe, Tomohiko</au><au>Akechi, Yuji</au><au>Ikeda, Remina</au><au>Nishio, Ren</au><au>Terabayashi, Kei</au><au>Ishii, Kyoko</au><au>Matsumi, Yoshiaki</au><au>Ashla, An Afida</au><au>Okamoto, Hideharu</au><au>Takubo, Kazuko</au><au>Matsuoka, Saori</au><au>Watanabe, Yumi</au><au>Hoshikawa, Yoshiko</au><au>Kurimasa, Akihiro</au><au>Shiota, Goshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthetic retinoid CD437 induces mitochondria-mediated apoptosis in hepatocellular carcinoma cells</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2008-06-13</date><risdate>2008</risdate><volume>370</volume><issue>4</issue><spage>629</spage><epage>633</epage><pages>629-633</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Retinoids play an important role in the regulation of cell growth and death. Synthetic retinoid CD437 reportedly induces apoptosis in various cancer cell lines. However, the mechanism of inducing apoptosis in hepatocellular carcinoma (HCC) cells by this agent remains to be clarified. In this study, we investigated the signaling pathway by which CD437 induces apoptosis in HCC cell lines. Apoptosis of six human HCC cell lines was induced by treatment with CD437. Caspase-3 and -9 were activated by CD437, suggesting that the apoptosis is mediated by mitochondrial pathways. Consistent with these findings, the treatment with CD437 upregulated Bax protein, downregulated Bcl-2 protein and released cytochrome
c into the cytoplasm. Moreover, rhodamine123 staining revealed mitochondrial depolarization in the cells treated with CD437. These data of the present study suggest that CD437 induces apoptosis in HCC cells via mitochondrial pathways.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>18406343</pmid><doi>10.1016/j.bbrc.2008.04.008</doi><tpages>5</tpages></addata></record> |
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subjects | Apoptosis bcl-2-Associated X Protein - metabolism Carcinoma, Hepatocellular - metabolism Caspase 3 - metabolism Caspase 9 - metabolism CD437 Cell Line, Tumor Cell Proliferation - drug effects Hepatocellular carcinoma Humans Liver Neoplasms - metabolism Mitochondria Mitochondria - drug effects Mitochondria - metabolism Proto-Oncogene Proteins c-bcl-2 - antagonists & inhibitors Proto-Oncogene Proteins c-bcl-2 - metabolism Retinoids - pharmacology Synthetic retinoid |
title | Synthetic retinoid CD437 induces mitochondria-mediated apoptosis in hepatocellular carcinoma cells |
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