Suppression of chondrosarcoma cells by 15-deoxy-Delta 12,14-prostaglandin J2 is associated with altered expression of Bax/Bcl-xL and p21
We previously reported that 15-deoxy-Delta(12,14)-prostaglandin J(2) (15d-PGJ(2)), the most potent agonist for peroxisome proliferator-activated receptor gamma (PPAR gamma), induces apoptosis of human chondrosarcoma cell line OUMS-27. The current study aimed to explore the mechanism of 15d-PGJ(2)-in...
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Veröffentlicht in: | Biochemical and biophysical research communications 2005-03, Vol.328 (2), p.375-382 |
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creator | Shen, Zheng-Nan Nishida, Keiichiro Doi, Hideyuki Oohashi, Toshitaka Hirohata, Satoshi Ozaki, Toshifumi Yoshida, Aki Ninomiya, Yoshifumi Inoue, Hajime |
description | We previously reported that 15-deoxy-Delta(12,14)-prostaglandin J(2) (15d-PGJ(2)), the most potent agonist for peroxisome proliferator-activated receptor gamma (PPAR gamma), induces apoptosis of human chondrosarcoma cell line OUMS-27. The current study aimed to explore the mechanism of 15d-PGJ(2)-induced apoptosis and inhibition of cell proliferation in OUMS-27 cells. The preliminary results of cDNA microarray analysis showed the down-regulation of anti-apoptotic Bcl-xL and up-regulation of pro-apoptotic Bax in the process of 15d-PGJ(2)-induced apoptosis. These changes were further confirmed at mRNA and protein levels by RT-PCR and Western blot analysis, respectively. Among cyclin-dependent kinase inhibitors, p21 was induced and up-regulated by 15d-PGJ(2), but p16 and p27 were not changed, suggesting that the involvement of p21 in inhibition of cell proliferation. Activation of caspase-3 by 15d-PGJ(2) was partly, but not completely, blocked by PPAR gamma antagonist (GW9662) suggesting the 15d-PGJ(2) exerted its effect by PPAR gamma-dependent and -independent pathways. Interestingly, immunohistochemical study on human chondrosarcoma samples revealed that Bcl-xL is frequently expressed by tumor cells. The results of the current study suggest that the potential ability of 15d-PGJ(2) in regulation of cell cycle and inhibition of Bcl-xL expression might be beneficial in the development of novel pharmacological agents for chondrosarcoma. |
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The current study aimed to explore the mechanism of 15d-PGJ(2)-induced apoptosis and inhibition of cell proliferation in OUMS-27 cells. The preliminary results of cDNA microarray analysis showed the down-regulation of anti-apoptotic Bcl-xL and up-regulation of pro-apoptotic Bax in the process of 15d-PGJ(2)-induced apoptosis. These changes were further confirmed at mRNA and protein levels by RT-PCR and Western blot analysis, respectively. Among cyclin-dependent kinase inhibitors, p21 was induced and up-regulated by 15d-PGJ(2), but p16 and p27 were not changed, suggesting that the involvement of p21 in inhibition of cell proliferation. Activation of caspase-3 by 15d-PGJ(2) was partly, but not completely, blocked by PPAR gamma antagonist (GW9662) suggesting the 15d-PGJ(2) exerted its effect by PPAR gamma-dependent and -independent pathways. Interestingly, immunohistochemical study on human chondrosarcoma samples revealed that Bcl-xL is frequently expressed by tumor cells. The results of the current study suggest that the potential ability of 15d-PGJ(2) in regulation of cell cycle and inhibition of Bcl-xL expression might be beneficial in the development of novel pharmacological agents for chondrosarcoma.</description><identifier>ISSN: 0006-291X</identifier><identifier>PMID: 15694358</identifier><language>eng</language><publisher>United States</publisher><subject>Apoptosis - drug effects ; bcl-2-Associated X Protein ; bcl-X Protein ; Cell Cycle - drug effects ; Cell Cycle Proteins - metabolism ; Cell Line, Tumor ; Cell Proliferation - drug effects ; Chondrosarcoma - metabolism ; Chondrosarcoma - pathology ; Cyclin-Dependent Kinase Inhibitor p21 ; Dose-Response Relationship, Drug ; Gene Expression Regulation, Neoplastic - drug effects ; Humans ; Prostaglandin D2 - analogs & derivatives ; Prostaglandin D2 - pharmacology ; Proto-Oncogene Proteins c-bcl-2 - metabolism</subject><ispartof>Biochemical and biophysical research communications, 2005-03, Vol.328 (2), p.375-382</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15694358$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shen, Zheng-Nan</creatorcontrib><creatorcontrib>Nishida, Keiichiro</creatorcontrib><creatorcontrib>Doi, Hideyuki</creatorcontrib><creatorcontrib>Oohashi, Toshitaka</creatorcontrib><creatorcontrib>Hirohata, Satoshi</creatorcontrib><creatorcontrib>Ozaki, Toshifumi</creatorcontrib><creatorcontrib>Yoshida, Aki</creatorcontrib><creatorcontrib>Ninomiya, Yoshifumi</creatorcontrib><creatorcontrib>Inoue, Hajime</creatorcontrib><title>Suppression of chondrosarcoma cells by 15-deoxy-Delta 12,14-prostaglandin J2 is associated with altered expression of Bax/Bcl-xL and p21</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>We previously reported that 15-deoxy-Delta(12,14)-prostaglandin J(2) (15d-PGJ(2)), the most potent agonist for peroxisome proliferator-activated receptor gamma (PPAR gamma), induces apoptosis of human chondrosarcoma cell line OUMS-27. The current study aimed to explore the mechanism of 15d-PGJ(2)-induced apoptosis and inhibition of cell proliferation in OUMS-27 cells. The preliminary results of cDNA microarray analysis showed the down-regulation of anti-apoptotic Bcl-xL and up-regulation of pro-apoptotic Bax in the process of 15d-PGJ(2)-induced apoptosis. These changes were further confirmed at mRNA and protein levels by RT-PCR and Western blot analysis, respectively. Among cyclin-dependent kinase inhibitors, p21 was induced and up-regulated by 15d-PGJ(2), but p16 and p27 were not changed, suggesting that the involvement of p21 in inhibition of cell proliferation. Activation of caspase-3 by 15d-PGJ(2) was partly, but not completely, blocked by PPAR gamma antagonist (GW9662) suggesting the 15d-PGJ(2) exerted its effect by PPAR gamma-dependent and -independent pathways. Interestingly, immunohistochemical study on human chondrosarcoma samples revealed that Bcl-xL is frequently expressed by tumor cells. The results of the current study suggest that the potential ability of 15d-PGJ(2) in regulation of cell cycle and inhibition of Bcl-xL expression might be beneficial in the development of novel pharmacological agents for chondrosarcoma.</description><subject>Apoptosis - drug effects</subject><subject>bcl-2-Associated X Protein</subject><subject>bcl-X Protein</subject><subject>Cell Cycle - drug effects</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Chondrosarcoma - metabolism</subject><subject>Chondrosarcoma - pathology</subject><subject>Cyclin-Dependent Kinase Inhibitor p21</subject><subject>Dose-Response Relationship, Drug</subject><subject>Gene Expression Regulation, Neoplastic - drug effects</subject><subject>Humans</subject><subject>Prostaglandin D2 - analogs & derivatives</subject><subject>Prostaglandin D2 - pharmacology</subject><subject>Proto-Oncogene Proteins c-bcl-2 - metabolism</subject><issn>0006-291X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkMtOwzAQRb0A0VL4BeQVKyxsx3GcJS1vVWJBF-yiiT2hQUkc4kSkf8Bnk4oisbqa0ZnHvUdkzjnXTKbibUZOQ_jgXAil0xMyE7FOVRSbOfl-Hdq2wxBK31BfULv1jet8gM76GqjFqgo031ERM4d-3LFbrHqgQl4JxdoJ7OG9gsaVDX2WtAwUQvC2hB4d_Sr7LYWqx24qcPx_Zgnj9dJWbFzTaZi2UpyR4wKqgOcHXZDN_d1m9cjWLw9Pq5s1a2NlmLZxpDAxTitjdZEWuU6EQxCRzGODuTa2QMiVAS6mTiJNIaLcGSmSAgXwaEEuf9dOv38OGPqsLsPeJTToh5DpRPFUJnvw4gAOeY0ua7uyhm6X_UUX_QCVYmob</recordid><startdate>20050311</startdate><enddate>20050311</enddate><creator>Shen, Zheng-Nan</creator><creator>Nishida, Keiichiro</creator><creator>Doi, Hideyuki</creator><creator>Oohashi, Toshitaka</creator><creator>Hirohata, Satoshi</creator><creator>Ozaki, Toshifumi</creator><creator>Yoshida, Aki</creator><creator>Ninomiya, Yoshifumi</creator><creator>Inoue, Hajime</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20050311</creationdate><title>Suppression of chondrosarcoma cells by 15-deoxy-Delta 12,14-prostaglandin J2 is associated with altered expression of Bax/Bcl-xL and p21</title><author>Shen, Zheng-Nan ; Nishida, Keiichiro ; Doi, Hideyuki ; Oohashi, Toshitaka ; Hirohata, Satoshi ; Ozaki, Toshifumi ; Yoshida, Aki ; Ninomiya, Yoshifumi ; Inoue, Hajime</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p548-6c534e78d648c6f9fb671dea132b58eb68cfeab48a012b5728f13bd8217fe1a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Apoptosis - drug effects</topic><topic>bcl-2-Associated X Protein</topic><topic>bcl-X Protein</topic><topic>Cell Cycle - drug effects</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>Chondrosarcoma - metabolism</topic><topic>Chondrosarcoma - pathology</topic><topic>Cyclin-Dependent Kinase Inhibitor p21</topic><topic>Dose-Response Relationship, Drug</topic><topic>Gene Expression Regulation, Neoplastic - drug effects</topic><topic>Humans</topic><topic>Prostaglandin D2 - analogs & derivatives</topic><topic>Prostaglandin D2 - pharmacology</topic><topic>Proto-Oncogene Proteins c-bcl-2 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shen, Zheng-Nan</creatorcontrib><creatorcontrib>Nishida, Keiichiro</creatorcontrib><creatorcontrib>Doi, Hideyuki</creatorcontrib><creatorcontrib>Oohashi, Toshitaka</creatorcontrib><creatorcontrib>Hirohata, Satoshi</creatorcontrib><creatorcontrib>Ozaki, Toshifumi</creatorcontrib><creatorcontrib>Yoshida, Aki</creatorcontrib><creatorcontrib>Ninomiya, Yoshifumi</creatorcontrib><creatorcontrib>Inoue, Hajime</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</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>Shen, Zheng-Nan</au><au>Nishida, Keiichiro</au><au>Doi, Hideyuki</au><au>Oohashi, Toshitaka</au><au>Hirohata, Satoshi</au><au>Ozaki, Toshifumi</au><au>Yoshida, Aki</au><au>Ninomiya, Yoshifumi</au><au>Inoue, Hajime</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Suppression of chondrosarcoma cells by 15-deoxy-Delta 12,14-prostaglandin J2 is associated with altered expression of Bax/Bcl-xL and p21</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2005-03-11</date><risdate>2005</risdate><volume>328</volume><issue>2</issue><spage>375</spage><epage>382</epage><pages>375-382</pages><issn>0006-291X</issn><abstract>We previously reported that 15-deoxy-Delta(12,14)-prostaglandin J(2) (15d-PGJ(2)), the most potent agonist for peroxisome proliferator-activated receptor gamma (PPAR gamma), induces apoptosis of human chondrosarcoma cell line OUMS-27. The current study aimed to explore the mechanism of 15d-PGJ(2)-induced apoptosis and inhibition of cell proliferation in OUMS-27 cells. The preliminary results of cDNA microarray analysis showed the down-regulation of anti-apoptotic Bcl-xL and up-regulation of pro-apoptotic Bax in the process of 15d-PGJ(2)-induced apoptosis. These changes were further confirmed at mRNA and protein levels by RT-PCR and Western blot analysis, respectively. Among cyclin-dependent kinase inhibitors, p21 was induced and up-regulated by 15d-PGJ(2), but p16 and p27 were not changed, suggesting that the involvement of p21 in inhibition of cell proliferation. Activation of caspase-3 by 15d-PGJ(2) was partly, but not completely, blocked by PPAR gamma antagonist (GW9662) suggesting the 15d-PGJ(2) exerted its effect by PPAR gamma-dependent and -independent pathways. Interestingly, immunohistochemical study on human chondrosarcoma samples revealed that Bcl-xL is frequently expressed by tumor cells. The results of the current study suggest that the potential ability of 15d-PGJ(2) in regulation of cell cycle and inhibition of Bcl-xL expression might be beneficial in the development of novel pharmacological agents for chondrosarcoma.</abstract><cop>United States</cop><pmid>15694358</pmid><tpages>8</tpages></addata></record> |
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subjects | Apoptosis - drug effects bcl-2-Associated X Protein bcl-X Protein Cell Cycle - drug effects Cell Cycle Proteins - metabolism Cell Line, Tumor Cell Proliferation - drug effects Chondrosarcoma - metabolism Chondrosarcoma - pathology Cyclin-Dependent Kinase Inhibitor p21 Dose-Response Relationship, Drug Gene Expression Regulation, Neoplastic - drug effects Humans Prostaglandin D2 - analogs & derivatives Prostaglandin D2 - pharmacology Proto-Oncogene Proteins c-bcl-2 - metabolism |
title | Suppression of chondrosarcoma cells by 15-deoxy-Delta 12,14-prostaglandin J2 is associated with altered expression of Bax/Bcl-xL and p21 |
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