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
Hauptverfasser: 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
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container_issue 8
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container_title Cell biology international
container_volume 32
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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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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source MEDLINE; Wiley Online Library Journals Frontfile Complete
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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