Induction of G1 phase arrest and apoptosis in MDA-MB-231 breast cancer cells by troglitazone, a synthetic peroxisome proliferator-activated receptor γ (PPARγ) ligand
Peroxisome proliferator‐activated receptor γ (PPARγ) ligands inhibit cell proliferation and induce apoptosis in cancer cells. Here we wished to determine whether the PPARγ ligand induces apoptosis and cell cycle arrest of the MDA‐MB‐231 cell, an estrogen receptor α negative breast cancer cell line....
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Veröffentlicht in: | Cell biology international 2008-08, Vol.32 (8), p.906-912 |
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creator | Yu, Hong-Nu Lee, Young-Rae Noh, Eun-Mi Lee, Kyung-Sun Kim, Jong-Suk Song, Eun-Kyung Han, Myung-Kwan Lee, Yong-Chul Kwon, Kang-Beom Lee, Seung-Jin Youn, Hyun Jo Jung, Sung Hoo |
description | Peroxisome proliferator‐activated receptor γ (PPARγ) ligands inhibit cell proliferation and induce apoptosis in cancer cells. Here we wished to determine whether the PPARγ ligand induces apoptosis and cell cycle arrest of the MDA‐MB‐231 cell, an estrogen receptor α negative breast cancer cell line. The treatment of MDA‐MB‐231 cell with PPARγ ligands was shown to induce inhibition of cell growth in a dose‐dependent manner as determined by MTT assay. Cell cycle analysis showed a G1 arrest in MDA‐MB‐231 cells exposed to troglitazone. An apoptotic effect by troglitazone demonstrated that apoptotic cells elevated by 2.5‐fold from the control level at 10 μM, to 3.1‐fold at 50 μM and to 3.5‐fold at 75 μM. Moreover, troglitazone treatment, applied in a dose‐dependent manner, caused a marked decrease in pRb, cyclin D1, cyclin D2, cyclin D3, Cdk2, Cdk4 and Cdk6 expression as well as a significant increase in p21 and p27 expression. These results indicate that troglitazone causes growth inhibition, G1 arrest and apoptotic death of MDA‐MB‐231 cells. |
doi_str_mv | 10.1016/j.cellbi.2008.04.011 |
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Here we wished to determine whether the PPARγ ligand induces apoptosis and cell cycle arrest of the MDA‐MB‐231 cell, an estrogen receptor α negative breast cancer cell line. The treatment of MDA‐MB‐231 cell with PPARγ ligands was shown to induce inhibition of cell growth in a dose‐dependent manner as determined by MTT assay. Cell cycle analysis showed a G1 arrest in MDA‐MB‐231 cells exposed to troglitazone. An apoptotic effect by troglitazone demonstrated that apoptotic cells elevated by 2.5‐fold from the control level at 10 μM, to 3.1‐fold at 50 μM and to 3.5‐fold at 75 μM. Moreover, troglitazone treatment, applied in a dose‐dependent manner, caused a marked decrease in pRb, cyclin D1, cyclin D2, cyclin D3, Cdk2, Cdk4 and Cdk6 expression as well as a significant increase in p21 and p27 expression. These results indicate that troglitazone causes growth inhibition, G1 arrest and apoptotic death of MDA‐MB‐231 cells.</description><identifier>ISSN: 1065-6995</identifier><identifier>EISSN: 1095-8355</identifier><identifier>DOI: 10.1016/j.cellbi.2008.04.011</identifier><identifier>PMID: 18474441</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Antineoplastic Agents - pharmacology ; Apoptosis ; Apoptosis - drug effects ; Breast Neoplasms - metabolism ; Breast Neoplasms - pathology ; Cell cycle ; Cell Line, Tumor ; Cell Proliferation - drug effects ; Chromans - pharmacology ; Cyclin-Dependent Kinase Inhibitor p21 - metabolism ; Cyclin-Dependent Kinases - metabolism ; Cyclins - metabolism ; G1 Phase - drug effects ; Humans ; Ligands ; PPAR gamma - metabolism ; PPARγ ligand ; Proliferating Cell Nuclear Antigen - metabolism ; Thiazolidinediones - pharmacology ; Troglitazone</subject><ispartof>Cell biology international, 2008-08, Vol.32 (8), p.906-912</ispartof><rights>The Author(s) Journal compilation © 2008 International Federation for Cell Biology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1016%2Fj.cellbi.2008.04.011$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1016%2Fj.cellbi.2008.04.011$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18474441$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Hong-Nu</creatorcontrib><creatorcontrib>Lee, Young-Rae</creatorcontrib><creatorcontrib>Noh, Eun-Mi</creatorcontrib><creatorcontrib>Lee, Kyung-Sun</creatorcontrib><creatorcontrib>Kim, Jong-Suk</creatorcontrib><creatorcontrib>Song, Eun-Kyung</creatorcontrib><creatorcontrib>Han, Myung-Kwan</creatorcontrib><creatorcontrib>Lee, Yong-Chul</creatorcontrib><creatorcontrib>Kwon, Kang-Beom</creatorcontrib><creatorcontrib>Lee, Seung-Jin</creatorcontrib><creatorcontrib>Youn, Hyun Jo</creatorcontrib><creatorcontrib>Jung, Sung Hoo</creatorcontrib><title>Induction of G1 phase arrest and apoptosis in MDA-MB-231 breast cancer cells by troglitazone, a synthetic peroxisome proliferator-activated receptor γ (PPARγ) ligand</title><title>Cell biology international</title><addtitle>Cell Biol Int</addtitle><description>Peroxisome proliferator‐activated receptor γ (PPARγ) ligands inhibit cell proliferation and induce apoptosis in cancer cells. Here we wished to determine whether the PPARγ ligand induces apoptosis and cell cycle arrest of the MDA‐MB‐231 cell, an estrogen receptor α negative breast cancer cell line. The treatment of MDA‐MB‐231 cell with PPARγ ligands was shown to induce inhibition of cell growth in a dose‐dependent manner as determined by MTT assay. Cell cycle analysis showed a G1 arrest in MDA‐MB‐231 cells exposed to troglitazone. An apoptotic effect by troglitazone demonstrated that apoptotic cells elevated by 2.5‐fold from the control level at 10 μM, to 3.1‐fold at 50 μM and to 3.5‐fold at 75 μM. Moreover, troglitazone treatment, applied in a dose‐dependent manner, caused a marked decrease in pRb, cyclin D1, cyclin D2, cyclin D3, Cdk2, Cdk4 and Cdk6 expression as well as a significant increase in p21 and p27 expression. These results indicate that troglitazone causes growth inhibition, G1 arrest and apoptotic death of MDA‐MB‐231 cells.</description><subject>Antineoplastic Agents - pharmacology</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - pathology</subject><subject>Cell cycle</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Chromans - pharmacology</subject><subject>Cyclin-Dependent Kinase Inhibitor p21 - metabolism</subject><subject>Cyclin-Dependent Kinases - metabolism</subject><subject>Cyclins - metabolism</subject><subject>G1 Phase - drug effects</subject><subject>Humans</subject><subject>Ligands</subject><subject>PPAR gamma - metabolism</subject><subject>PPARγ ligand</subject><subject>Proliferating Cell Nuclear Antigen - metabolism</subject><subject>Thiazolidinediones - pharmacology</subject><subject>Troglitazone</subject><issn>1065-6995</issn><issn>1095-8355</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkVFu1DAQhiMEoqVwA4T8hEAiwY4dO-nbdmGXldpSIaCPlu1MWi_ZONhe6HIhDtB79Ew42gJPHsnfP_PP_Fn2nOCCYMLfrgsDfa9tUWJcF5gVmJAH2SHBTZXXtKoeTjWvct401UH2JIQ1TgSr-ePsgNRMMMbIYfZ7NbRbE60bkOvQkqDxWgVAynsIEamhRWp0Y3TBBmQHdPZulp-d5CUlSHtQCTFqMODR5CUgvUPRu6veRvXLDfAGKRR2Q7yGaA0awbsbG9wG0OhdbzvwKjqfqzT-h4rQIg8G0iyP7m7Rq4uL2ae729eot1fJxtPsUaf6AM_u36Psy-L95_mH_PTjcjWfnea2JJTmJeFlrXXbma7WvBRdUxOCWVdxrHQtgLQdbXlbAedGk47phjQGhOaaCtYaQY-yl_u-yeL3bbqB3NgwLacGcNsgeUOZKCucwBf34FZvoJWjtxvld_LvaRNwvAd-2h52__-xnOKTa7mPT07xScxkCkfOT1bnZSNoEud7sQ0Rbv6Jlf8muaCikpfnSzm_XHAsvi4kp38AUxWhvA</recordid><startdate>200808</startdate><enddate>200808</enddate><creator>Yu, Hong-Nu</creator><creator>Lee, Young-Rae</creator><creator>Noh, Eun-Mi</creator><creator>Lee, Kyung-Sun</creator><creator>Kim, Jong-Suk</creator><creator>Song, Eun-Kyung</creator><creator>Han, Myung-Kwan</creator><creator>Lee, Yong-Chul</creator><creator>Kwon, Kang-Beom</creator><creator>Lee, Seung-Jin</creator><creator>Youn, Hyun Jo</creator><creator>Jung, Sung Hoo</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200808</creationdate><title>Induction of G1 phase arrest and apoptosis in MDA-MB-231 breast cancer cells by troglitazone, a synthetic peroxisome proliferator-activated receptor γ (PPARγ) ligand</title><author>Yu, Hong-Nu ; Lee, Young-Rae ; Noh, Eun-Mi ; Lee, Kyung-Sun ; Kim, Jong-Suk ; Song, Eun-Kyung ; Han, Myung-Kwan ; Lee, Yong-Chul ; Kwon, Kang-Beom ; Lee, Seung-Jin ; Youn, Hyun Jo ; Jung, Sung Hoo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i2133-21628bbdfcf8b627f981104f560ab87e1df3d6d5e66cb1f4b919ce7b6b374dc73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Antineoplastic Agents - pharmacology</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - pathology</topic><topic>Cell cycle</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>Chromans - pharmacology</topic><topic>Cyclin-Dependent Kinase Inhibitor p21 - metabolism</topic><topic>Cyclin-Dependent Kinases - metabolism</topic><topic>Cyclins - metabolism</topic><topic>G1 Phase - drug effects</topic><topic>Humans</topic><topic>Ligands</topic><topic>PPAR gamma - metabolism</topic><topic>PPARγ ligand</topic><topic>Proliferating Cell Nuclear Antigen - metabolism</topic><topic>Thiazolidinediones - pharmacology</topic><topic>Troglitazone</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Hong-Nu</creatorcontrib><creatorcontrib>Lee, Young-Rae</creatorcontrib><creatorcontrib>Noh, Eun-Mi</creatorcontrib><creatorcontrib>Lee, Kyung-Sun</creatorcontrib><creatorcontrib>Kim, Jong-Suk</creatorcontrib><creatorcontrib>Song, Eun-Kyung</creatorcontrib><creatorcontrib>Han, Myung-Kwan</creatorcontrib><creatorcontrib>Lee, Yong-Chul</creatorcontrib><creatorcontrib>Kwon, Kang-Beom</creatorcontrib><creatorcontrib>Lee, Seung-Jin</creatorcontrib><creatorcontrib>Youn, Hyun Jo</creatorcontrib><creatorcontrib>Jung, Sung Hoo</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Cell biology international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Hong-Nu</au><au>Lee, Young-Rae</au><au>Noh, Eun-Mi</au><au>Lee, Kyung-Sun</au><au>Kim, Jong-Suk</au><au>Song, Eun-Kyung</au><au>Han, Myung-Kwan</au><au>Lee, Yong-Chul</au><au>Kwon, Kang-Beom</au><au>Lee, Seung-Jin</au><au>Youn, Hyun Jo</au><au>Jung, Sung Hoo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of G1 phase arrest and apoptosis in MDA-MB-231 breast cancer cells by troglitazone, a synthetic peroxisome proliferator-activated receptor γ (PPARγ) ligand</atitle><jtitle>Cell biology international</jtitle><addtitle>Cell Biol Int</addtitle><date>2008-08</date><risdate>2008</risdate><volume>32</volume><issue>8</issue><spage>906</spage><epage>912</epage><pages>906-912</pages><issn>1065-6995</issn><eissn>1095-8355</eissn><abstract>Peroxisome proliferator‐activated receptor γ (PPARγ) ligands inhibit cell proliferation and induce apoptosis in cancer cells. Here we wished to determine whether the PPARγ ligand induces apoptosis and cell cycle arrest of the MDA‐MB‐231 cell, an estrogen receptor α negative breast cancer cell line. The treatment of MDA‐MB‐231 cell with PPARγ ligands was shown to induce inhibition of cell growth in a dose‐dependent manner as determined by MTT assay. Cell cycle analysis showed a G1 arrest in MDA‐MB‐231 cells exposed to troglitazone. An apoptotic effect by troglitazone demonstrated that apoptotic cells elevated by 2.5‐fold from the control level at 10 μM, to 3.1‐fold at 50 μM and to 3.5‐fold at 75 μM. Moreover, troglitazone treatment, applied in a dose‐dependent manner, caused a marked decrease in pRb, cyclin D1, cyclin D2, cyclin D3, Cdk2, Cdk4 and Cdk6 expression as well as a significant increase in p21 and p27 expression. These results indicate that troglitazone causes growth inhibition, G1 arrest and apoptotic death of MDA‐MB‐231 cells.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>18474441</pmid><doi>10.1016/j.cellbi.2008.04.011</doi><tpages>7</tpages></addata></record> |
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subjects | Antineoplastic Agents - pharmacology Apoptosis Apoptosis - drug effects Breast Neoplasms - metabolism Breast Neoplasms - pathology Cell cycle Cell Line, Tumor Cell Proliferation - drug effects Chromans - pharmacology Cyclin-Dependent Kinase Inhibitor p21 - metabolism Cyclin-Dependent Kinases - metabolism Cyclins - metabolism G1 Phase - drug effects Humans Ligands PPAR gamma - metabolism PPARγ ligand Proliferating Cell Nuclear Antigen - metabolism Thiazolidinediones - pharmacology Troglitazone |
title | Induction of G1 phase arrest and apoptosis in MDA-MB-231 breast cancer cells by troglitazone, a synthetic peroxisome proliferator-activated receptor γ (PPARγ) ligand |
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