Overexpression and poly-ubiquitylation of the DEAD-box RNA helicase p68 in colorectal tumours
The DEAD box RNA helicase, p68, is upregulated in exponentially growing cells and shows cell cycle-dependent changes in nuclear localization. Although some other DEAD box proteins have been implicated in cancer, there have been no reports of any link between p68 status and carcinogenesis. In the pre...
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Veröffentlicht in: | Oncogene 2001-11, Vol.20 (53), p.7734-7743 |
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description | The DEAD box RNA helicase, p68, is upregulated in exponentially growing cells and shows cell cycle-dependent changes in nuclear localization. Although some other DEAD box proteins have been implicated in cancer, there have been no reports of any link between p68 status and carcinogenesis. In the present study we have analysed specimens from 50 patients with colorectal adenocarcinomas, including cases in which an adenomatous polyp was also present, by immunohistochemistry and Western blotting. Our data indicate that p68 protein is consistently overexpressed in tumours as compared with matched normal tissue. Examination of the levels of p68 mRNA from both normal and tumour tissue showed no obvious specific increase in p68 mRNA levels in tumours nor any evidence of underlying mutations in the p68 coding region. Interestingly, however, the accumulated p68 appears to be poly-ubiquitylated, suggesting a possible defect in proteasome-mediated degradation in these tumours. This overexpression/ubiquitylation is observed in both pre-invasive and invasive lesions suggesting that the dysregulation of p68 expression occurs early during tumour development. Finally, we demonstrate that ubiquitylation of p68 occurs in cultured cells, thereby providing a model for the molecular analysis of this process and its potential role in tumorigenesis. |
doi_str_mv | 10.1038/sj.onc.1204976 |
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Gordon ; KERNOHAN, Neil M ; CAREY, Francis A ; KAY, Richard A ; STEELE, Robert J. C ; FULLER-PACE, Frances V</creator><creatorcontrib>CAUSEVIC, Mirsada ; HISLOP, R. Gordon ; KERNOHAN, Neil M ; CAREY, Francis A ; KAY, Richard A ; STEELE, Robert J. C ; FULLER-PACE, Frances V</creatorcontrib><description>The DEAD box RNA helicase, p68, is upregulated in exponentially growing cells and shows cell cycle-dependent changes in nuclear localization. Although some other DEAD box proteins have been implicated in cancer, there have been no reports of any link between p68 status and carcinogenesis. In the present study we have analysed specimens from 50 patients with colorectal adenocarcinomas, including cases in which an adenomatous polyp was also present, by immunohistochemistry and Western blotting. Our data indicate that p68 protein is consistently overexpressed in tumours as compared with matched normal tissue. Examination of the levels of p68 mRNA from both normal and tumour tissue showed no obvious specific increase in p68 mRNA levels in tumours nor any evidence of underlying mutations in the p68 coding region. Interestingly, however, the accumulated p68 appears to be poly-ubiquitylated, suggesting a possible defect in proteasome-mediated degradation in these tumours. This overexpression/ubiquitylation is observed in both pre-invasive and invasive lesions suggesting that the dysregulation of p68 expression occurs early during tumour development. Finally, we demonstrate that ubiquitylation of p68 occurs in cultured cells, thereby providing a model for the molecular analysis of this process and its potential role in tumorigenesis.</description><identifier>ISSN: 0950-9232</identifier><identifier>EISSN: 1476-5594</identifier><identifier>DOI: 10.1038/sj.onc.1204976</identifier><identifier>PMID: 11753651</identifier><identifier>CODEN: ONCNES</identifier><language>eng</language><publisher>Basingstoke: Nature Publishing</publisher><subject>Animals ; Antibodies ; Biological and medical sciences ; Blotting, Western ; Cancer ; Carcinogenesis ; Cell cycle ; Cell growth ; Colorectal cancer ; Colorectal Neoplasms - enzymology ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - metabolism ; Colorectal Neoplasms - pathology ; COS Cells ; DEAD box proteins ; DEAD-box RNA Helicases ; DNA helicase ; Fundamental and applied biological sciences. Psychology ; HeLa Cells ; Humans ; Immunohistochemistry ; Invasiveness ; Localization ; Molecular and cellular biology ; Molecular Weight ; mRNA ; p68 Protein ; Polyps ; Polyubiquitin - metabolism ; Proteasomes ; Protein Kinases - biosynthesis ; Protein Kinases - chemistry ; Protein Kinases - genetics ; Protein Kinases - metabolism ; Proteins ; Reverse Transcriptase Polymerase Chain Reaction ; RNA helicase ; RNA Helicases - biosynthesis ; RNA Helicases - chemistry ; RNA Helicases - genetics ; RNA Helicases - metabolism ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Transfection ; Tumorigenesis ; Tumors ; Ubiquitin ; Western blotting</subject><ispartof>Oncogene, 2001-11, Vol.20 (53), p.7734-7743</ispartof><rights>2002 INIST-CNRS</rights><rights>COPYRIGHT 2001 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Nov 22, 2001</rights><rights>Macmillan Publishers Limited 2001.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c516t-fcdc2785293ff5b7a6a0bb29f551516a5c47332f025895b68d66632e653555573</citedby><cites>FETCH-LOGICAL-c516t-fcdc2785293ff5b7a6a0bb29f551516a5c47332f025895b68d66632e653555573</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14159134$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11753651$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CAUSEVIC, Mirsada</creatorcontrib><creatorcontrib>HISLOP, R. Gordon</creatorcontrib><creatorcontrib>KERNOHAN, Neil M</creatorcontrib><creatorcontrib>CAREY, Francis A</creatorcontrib><creatorcontrib>KAY, Richard A</creatorcontrib><creatorcontrib>STEELE, Robert J. C</creatorcontrib><creatorcontrib>FULLER-PACE, Frances V</creatorcontrib><title>Overexpression and poly-ubiquitylation of the DEAD-box RNA helicase p68 in colorectal tumours</title><title>Oncogene</title><addtitle>Oncogene</addtitle><description>The DEAD box RNA helicase, p68, is upregulated in exponentially growing cells and shows cell cycle-dependent changes in nuclear localization. Although some other DEAD box proteins have been implicated in cancer, there have been no reports of any link between p68 status and carcinogenesis. In the present study we have analysed specimens from 50 patients with colorectal adenocarcinomas, including cases in which an adenomatous polyp was also present, by immunohistochemistry and Western blotting. Our data indicate that p68 protein is consistently overexpressed in tumours as compared with matched normal tissue. Examination of the levels of p68 mRNA from both normal and tumour tissue showed no obvious specific increase in p68 mRNA levels in tumours nor any evidence of underlying mutations in the p68 coding region. Interestingly, however, the accumulated p68 appears to be poly-ubiquitylated, suggesting a possible defect in proteasome-mediated degradation in these tumours. This overexpression/ubiquitylation is observed in both pre-invasive and invasive lesions suggesting that the dysregulation of p68 expression occurs early during tumour development. Finally, we demonstrate that ubiquitylation of p68 occurs in cultured cells, thereby providing a model for the molecular analysis of this process and its potential role in tumorigenesis.</description><subject>Animals</subject><subject>Antibodies</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Cancer</subject><subject>Carcinogenesis</subject><subject>Cell cycle</subject><subject>Cell growth</subject><subject>Colorectal cancer</subject><subject>Colorectal Neoplasms - enzymology</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>Colorectal Neoplasms - pathology</subject><subject>COS Cells</subject><subject>DEAD box proteins</subject><subject>DEAD-box RNA Helicases</subject><subject>DNA helicase</subject><subject>Fundamental and applied biological sciences. 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Gordon ; KERNOHAN, Neil M ; CAREY, Francis A ; KAY, Richard A ; STEELE, Robert J. 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Gordon</au><au>KERNOHAN, Neil M</au><au>CAREY, Francis A</au><au>KAY, Richard A</au><au>STEELE, Robert J. C</au><au>FULLER-PACE, Frances V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Overexpression and poly-ubiquitylation of the DEAD-box RNA helicase p68 in colorectal tumours</atitle><jtitle>Oncogene</jtitle><addtitle>Oncogene</addtitle><date>2001-11-22</date><risdate>2001</risdate><volume>20</volume><issue>53</issue><spage>7734</spage><epage>7743</epage><pages>7734-7743</pages><issn>0950-9232</issn><eissn>1476-5594</eissn><coden>ONCNES</coden><abstract>The DEAD box RNA helicase, p68, is upregulated in exponentially growing cells and shows cell cycle-dependent changes in nuclear localization. Although some other DEAD box proteins have been implicated in cancer, there have been no reports of any link between p68 status and carcinogenesis. In the present study we have analysed specimens from 50 patients with colorectal adenocarcinomas, including cases in which an adenomatous polyp was also present, by immunohistochemistry and Western blotting. Our data indicate that p68 protein is consistently overexpressed in tumours as compared with matched normal tissue. Examination of the levels of p68 mRNA from both normal and tumour tissue showed no obvious specific increase in p68 mRNA levels in tumours nor any evidence of underlying mutations in the p68 coding region. Interestingly, however, the accumulated p68 appears to be poly-ubiquitylated, suggesting a possible defect in proteasome-mediated degradation in these tumours. This overexpression/ubiquitylation is observed in both pre-invasive and invasive lesions suggesting that the dysregulation of p68 expression occurs early during tumour development. Finally, we demonstrate that ubiquitylation of p68 occurs in cultured cells, thereby providing a model for the molecular analysis of this process and its potential role in tumorigenesis.</abstract><cop>Basingstoke</cop><pub>Nature Publishing</pub><pmid>11753651</pmid><doi>10.1038/sj.onc.1204976</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibodies Biological and medical sciences Blotting, Western Cancer Carcinogenesis Cell cycle Cell growth Colorectal cancer Colorectal Neoplasms - enzymology Colorectal Neoplasms - genetics Colorectal Neoplasms - metabolism Colorectal Neoplasms - pathology COS Cells DEAD box proteins DEAD-box RNA Helicases DNA helicase Fundamental and applied biological sciences. Psychology HeLa Cells Humans Immunohistochemistry Invasiveness Localization Molecular and cellular biology Molecular Weight mRNA p68 Protein Polyps Polyubiquitin - metabolism Proteasomes Protein Kinases - biosynthesis Protein Kinases - chemistry Protein Kinases - genetics Protein Kinases - metabolism Proteins Reverse Transcriptase Polymerase Chain Reaction RNA helicase RNA Helicases - biosynthesis RNA Helicases - chemistry RNA Helicases - genetics RNA Helicases - metabolism RNA, Messenger - genetics RNA, Messenger - metabolism Transfection Tumorigenesis Tumors Ubiquitin Western blotting |
title | Overexpression and poly-ubiquitylation of the DEAD-box RNA helicase p68 in colorectal tumours |
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