Tripartite Motif Containing 28 (Trim28) Can Regulate Cell Proliferation by Bridging HDAC1/E2F Interactions
Trim28 is a poorly understood transcriptional co-factor with pleiotropic biological activities. Although Trim28 mRNA is found in many studies to be up-regulated in both lung and breast cancer tissues relative to normal adjacent tissue, we found that within a panel of early-stage lung adenocarcinomas...
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creator | Chen, Lu Chen, Dung-Tsa Kurtyka, Courtney Rawal, Bhupendra Fulp, William J. Haura, Eric B. Cress, W.Douglas |
description | Trim28 is a poorly understood transcriptional co-factor with pleiotropic biological activities. Although Trim28 mRNA is found in many studies to be up-regulated in both lung and breast cancer tissues relative to normal adjacent tissue, we found that within a panel of early-stage lung adenocarcinomas high levels of Trim28 protein correlate with better overall survival. This surprising observation suggests that Trim 28 may have anti-proliferative activity within tumors. To test this hypothesis, we used shRNAi to generate Trim28-knockdown breast and lung cancer cell lines and found that Trim28 depletion led to increased cell proliferation. Likewise, overexpression of Trim28 led to decreased cell proliferation. Confocal microscopy indicated co-localization of E2F3 and E2F4 with Trim28 within the cell nucleus, and co-immunoprecipitation assays demonstrated that Trim28 can bind both E2F3 and E2F4. Trim28 overexpression inhibited the transcriptional activity of E2F3 and E2F4, whereas Trim28 deficiency enhanced their activity. Co-immunoprecipitations further indicated that Trim28 bridges an interaction between E2Fs 3 and 4 and HDAC1. Promoter-reporter assays demonstrated that the ability of HDAC1 to repress E2F3 and E2F4-driven transcription is dependent on Trim28. Trim28 depletion increased E2F3 and E2F4 DNA binding activity, as measured by chromatin-immunoprecipitation (ChIP) assays while simultaneously reducing HDAC1 binding. Finally, ChIP-ReChIP experiments demonstrated that Trim/E2F complexes exist on several E2F-regulated promoters. Taken together, these results suggest that Trim28 has anti-proliferative activity in lung cancers via repression of members of the E2F family that are critical for cell proliferation.
Background: Trim28 appears up-regulated in many cancers.
Results: In early stage lung tumors high Trim28 correlates with increased overall survival and Trim28 reduces cell proliferation in model lung cancer cell lines through E2F interactions.
Conclusion: Trim28 may have a tumor suppressing role in the early stages of lung cancer.
Significance: These results suggest a complex role for Trim28 in lung cancer. |
doi_str_mv | 10.1074/jbc.M112.380865 |
format | Article |
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Background: Trim28 appears up-regulated in many cancers.
Results: In early stage lung tumors high Trim28 correlates with increased overall survival and Trim28 reduces cell proliferation in model lung cancer cell lines through E2F interactions.
Conclusion: Trim28 may have a tumor suppressing role in the early stages of lung cancer.
Significance: These results suggest a complex role for Trim28 in lung cancer.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M112.380865</identifier><identifier>PMID: 23060449</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Breast Neoplasms - genetics ; Breast Neoplasms - metabolism ; Breast Neoplasms - physiopathology ; Cancer ; Cell Cycle ; Cell Growth ; Cell Line, Tumor ; Cell Proliferation ; DNA - genetics ; DNA - metabolism ; E2F Transcription Factor ; E2F3 Transcription Factor - genetics ; E2F3 Transcription Factor - metabolism ; E2F4 Transcription Factor - genetics ; E2F4 Transcription Factor - metabolism ; Female ; Histone Deacetylase 1 - genetics ; Histone Deacetylase 1 - metabolism ; Humans ; Lung Cancer ; Lung Neoplasms - genetics ; Lung Neoplasms - metabolism ; Lung Neoplasms - physiopathology ; Male ; Molecular Bases of Disease ; Protein Binding ; Repressor Proteins - genetics ; Repressor Proteins - metabolism ; Tripartite Motif-Containing Protein 28</subject><ispartof>The Journal of biological chemistry, 2012-11, Vol.287 (48), p.40106-40118</ispartof><rights>2012 © 2012 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>2012 by The American Society for Biochemistry and Molecular Biology, Inc. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c509t-d660fd7af752e1b9b8be7e50849d0fe9c04fbd55c2abd8312907d35f3aaacfea3</citedby><cites>FETCH-LOGICAL-c509t-d660fd7af752e1b9b8be7e50849d0fe9c04fbd55c2abd8312907d35f3aaacfea3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504725/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504725/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23060449$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Lu</creatorcontrib><creatorcontrib>Chen, Dung-Tsa</creatorcontrib><creatorcontrib>Kurtyka, Courtney</creatorcontrib><creatorcontrib>Rawal, Bhupendra</creatorcontrib><creatorcontrib>Fulp, William J.</creatorcontrib><creatorcontrib>Haura, Eric B.</creatorcontrib><creatorcontrib>Cress, W.Douglas</creatorcontrib><title>Tripartite Motif Containing 28 (Trim28) Can Regulate Cell Proliferation by Bridging HDAC1/E2F Interactions</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Trim28 is a poorly understood transcriptional co-factor with pleiotropic biological activities. Although Trim28 mRNA is found in many studies to be up-regulated in both lung and breast cancer tissues relative to normal adjacent tissue, we found that within a panel of early-stage lung adenocarcinomas high levels of Trim28 protein correlate with better overall survival. This surprising observation suggests that Trim 28 may have anti-proliferative activity within tumors. To test this hypothesis, we used shRNAi to generate Trim28-knockdown breast and lung cancer cell lines and found that Trim28 depletion led to increased cell proliferation. Likewise, overexpression of Trim28 led to decreased cell proliferation. Confocal microscopy indicated co-localization of E2F3 and E2F4 with Trim28 within the cell nucleus, and co-immunoprecipitation assays demonstrated that Trim28 can bind both E2F3 and E2F4. Trim28 overexpression inhibited the transcriptional activity of E2F3 and E2F4, whereas Trim28 deficiency enhanced their activity. Co-immunoprecipitations further indicated that Trim28 bridges an interaction between E2Fs 3 and 4 and HDAC1. Promoter-reporter assays demonstrated that the ability of HDAC1 to repress E2F3 and E2F4-driven transcription is dependent on Trim28. Trim28 depletion increased E2F3 and E2F4 DNA binding activity, as measured by chromatin-immunoprecipitation (ChIP) assays while simultaneously reducing HDAC1 binding. Finally, ChIP-ReChIP experiments demonstrated that Trim/E2F complexes exist on several E2F-regulated promoters. Taken together, these results suggest that Trim28 has anti-proliferative activity in lung cancers via repression of members of the E2F family that are critical for cell proliferation.
Background: Trim28 appears up-regulated in many cancers.
Results: In early stage lung tumors high Trim28 correlates with increased overall survival and Trim28 reduces cell proliferation in model lung cancer cell lines through E2F interactions.
Conclusion: Trim28 may have a tumor suppressing role in the early stages of lung cancer.
Significance: These results suggest a complex role for Trim28 in lung cancer.</description><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - physiopathology</subject><subject>Cancer</subject><subject>Cell Cycle</subject><subject>Cell Growth</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>DNA - genetics</subject><subject>DNA - metabolism</subject><subject>E2F Transcription Factor</subject><subject>E2F3 Transcription Factor - genetics</subject><subject>E2F3 Transcription Factor - metabolism</subject><subject>E2F4 Transcription Factor - genetics</subject><subject>E2F4 Transcription Factor - metabolism</subject><subject>Female</subject><subject>Histone Deacetylase 1 - genetics</subject><subject>Histone Deacetylase 1 - metabolism</subject><subject>Humans</subject><subject>Lung Cancer</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - metabolism</subject><subject>Lung Neoplasms - physiopathology</subject><subject>Male</subject><subject>Molecular Bases of Disease</subject><subject>Protein Binding</subject><subject>Repressor Proteins - genetics</subject><subject>Repressor Proteins - metabolism</subject><subject>Tripartite Motif-Containing Protein 28</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc9vFCEUx4nR2LV69mY41sPs8mOYGS4mdWxtkzYaUxNvhIHHymYWVmCb9L-XzdZGD3Lh8D7vy3t8EHpLyZKSvl1tJrO8pZQt-UCGTjxDC0oG3nBBfzxHC0IYbSQTwwl6lfOG1NNK-hKdME460rZygTZ3ye90Kr4Avo3FOzzGULQPPqwxG_BZrW_Z8B6POuBvsN7PupIjzDP-muLsHSRdfAx4esAfk7frQ9_Vp_ORri7YJb4OpQLmQOTX6IXTc4Y3j_cp-n55cTdeNTdfPl-P5zeNEUSWxnYdcbbXrhcM6CSnYYIeBBlaaYkDaUjrJiuEYXqyA6dMkt5y4bjW2jjQ_BR9OObu9tMWrIFQkp7Vri6i04OK2qt_K8H_VOt4r7ggbc9EDTh7DEjx1x5yUVufTV1ZB4j7rChjRHS9bLuKro6oSTHnBO7pGUrUwZCqhtTBkDoaqh3v_p7uif-jpALyCED9o3sPSWXjIRiwPoEpykb_3_DfP4ygvA</recordid><startdate>20121123</startdate><enddate>20121123</enddate><creator>Chen, Lu</creator><creator>Chen, Dung-Tsa</creator><creator>Kurtyka, Courtney</creator><creator>Rawal, Bhupendra</creator><creator>Fulp, William J.</creator><creator>Haura, Eric B.</creator><creator>Cress, W.Douglas</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20121123</creationdate><title>Tripartite Motif Containing 28 (Trim28) Can Regulate Cell Proliferation by Bridging HDAC1/E2F Interactions</title><author>Chen, Lu ; Chen, Dung-Tsa ; Kurtyka, Courtney ; Rawal, Bhupendra ; Fulp, William J. ; Haura, Eric B. ; Cress, W.Douglas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c509t-d660fd7af752e1b9b8be7e50849d0fe9c04fbd55c2abd8312907d35f3aaacfea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - physiopathology</topic><topic>Cancer</topic><topic>Cell Cycle</topic><topic>Cell Growth</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation</topic><topic>DNA - genetics</topic><topic>DNA - metabolism</topic><topic>E2F Transcription Factor</topic><topic>E2F3 Transcription Factor - genetics</topic><topic>E2F3 Transcription Factor - metabolism</topic><topic>E2F4 Transcription Factor - genetics</topic><topic>E2F4 Transcription Factor - metabolism</topic><topic>Female</topic><topic>Histone Deacetylase 1 - genetics</topic><topic>Histone Deacetylase 1 - metabolism</topic><topic>Humans</topic><topic>Lung Cancer</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - metabolism</topic><topic>Lung Neoplasms - physiopathology</topic><topic>Male</topic><topic>Molecular Bases of Disease</topic><topic>Protein Binding</topic><topic>Repressor Proteins - genetics</topic><topic>Repressor Proteins - metabolism</topic><topic>Tripartite Motif-Containing Protein 28</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Lu</creatorcontrib><creatorcontrib>Chen, Dung-Tsa</creatorcontrib><creatorcontrib>Kurtyka, Courtney</creatorcontrib><creatorcontrib>Rawal, Bhupendra</creatorcontrib><creatorcontrib>Fulp, William J.</creatorcontrib><creatorcontrib>Haura, Eric B.</creatorcontrib><creatorcontrib>Cress, W.Douglas</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Lu</au><au>Chen, Dung-Tsa</au><au>Kurtyka, Courtney</au><au>Rawal, Bhupendra</au><au>Fulp, William J.</au><au>Haura, Eric B.</au><au>Cress, W.Douglas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tripartite Motif Containing 28 (Trim28) Can Regulate Cell Proliferation by Bridging HDAC1/E2F Interactions</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2012-11-23</date><risdate>2012</risdate><volume>287</volume><issue>48</issue><spage>40106</spage><epage>40118</epage><pages>40106-40118</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Trim28 is a poorly understood transcriptional co-factor with pleiotropic biological activities. Although Trim28 mRNA is found in many studies to be up-regulated in both lung and breast cancer tissues relative to normal adjacent tissue, we found that within a panel of early-stage lung adenocarcinomas high levels of Trim28 protein correlate with better overall survival. This surprising observation suggests that Trim 28 may have anti-proliferative activity within tumors. To test this hypothesis, we used shRNAi to generate Trim28-knockdown breast and lung cancer cell lines and found that Trim28 depletion led to increased cell proliferation. Likewise, overexpression of Trim28 led to decreased cell proliferation. Confocal microscopy indicated co-localization of E2F3 and E2F4 with Trim28 within the cell nucleus, and co-immunoprecipitation assays demonstrated that Trim28 can bind both E2F3 and E2F4. Trim28 overexpression inhibited the transcriptional activity of E2F3 and E2F4, whereas Trim28 deficiency enhanced their activity. Co-immunoprecipitations further indicated that Trim28 bridges an interaction between E2Fs 3 and 4 and HDAC1. Promoter-reporter assays demonstrated that the ability of HDAC1 to repress E2F3 and E2F4-driven transcription is dependent on Trim28. Trim28 depletion increased E2F3 and E2F4 DNA binding activity, as measured by chromatin-immunoprecipitation (ChIP) assays while simultaneously reducing HDAC1 binding. Finally, ChIP-ReChIP experiments demonstrated that Trim/E2F complexes exist on several E2F-regulated promoters. Taken together, these results suggest that Trim28 has anti-proliferative activity in lung cancers via repression of members of the E2F family that are critical for cell proliferation.
Background: Trim28 appears up-regulated in many cancers.
Results: In early stage lung tumors high Trim28 correlates with increased overall survival and Trim28 reduces cell proliferation in model lung cancer cell lines through E2F interactions.
Conclusion: Trim28 may have a tumor suppressing role in the early stages of lung cancer.
Significance: These results suggest a complex role for Trim28 in lung cancer.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23060449</pmid><doi>10.1074/jbc.M112.380865</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Breast Neoplasms - genetics Breast Neoplasms - metabolism Breast Neoplasms - physiopathology Cancer Cell Cycle Cell Growth Cell Line, Tumor Cell Proliferation DNA - genetics DNA - metabolism E2F Transcription Factor E2F3 Transcription Factor - genetics E2F3 Transcription Factor - metabolism E2F4 Transcription Factor - genetics E2F4 Transcription Factor - metabolism Female Histone Deacetylase 1 - genetics Histone Deacetylase 1 - metabolism Humans Lung Cancer Lung Neoplasms - genetics Lung Neoplasms - metabolism Lung Neoplasms - physiopathology Male Molecular Bases of Disease Protein Binding Repressor Proteins - genetics Repressor Proteins - metabolism Tripartite Motif-Containing Protein 28 |
title | Tripartite Motif Containing 28 (Trim28) Can Regulate Cell Proliferation by Bridging HDAC1/E2F Interactions |
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