Pathology and biology associated with the fragile FHIT gene and gene product
More than 12 years and >800 scientific publications after the discovery of the first gene at a chromosome fragile site, the FHIT gene at FRA3B, there are still questions to pursue concerning the selective advantage conferred to cells by loss of expression of FHIT, the most frequent target of alle...
Gespeichert in:
Veröffentlicht in: | Journal of cellular biochemistry 2010-04, Vol.109 (5), p.858-865 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 865 |
---|---|
container_issue | 5 |
container_start_page | 858 |
container_title | Journal of cellular biochemistry |
container_volume | 109 |
creator | Saldivar, Joshua C. Shibata, Hidetaka Huebner, Kay |
description | More than 12 years and >800 scientific publications after the discovery of the first gene at a chromosome fragile site, the FHIT gene at FRA3B, there are still questions to pursue concerning the selective advantage conferred to cells by loss of expression of FHIT, the most frequent target of allele deletion in precancerous lesions and cancers. These questions are considered in light of recent investigations of genetic and epigenetic alterations to the locus and in a retrospective consideration of biological roles of the Fhit protein discovered through functional studies. J. Cell. Biochem. 109: 858–865, 2010. © 2010 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/jcb.22481 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_968165457</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>968165457</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3941-f4aa9921032188448458074557c2597e8e04b22701ff597969ddb3065f3193403</originalsourceid><addsrcrecordid>eNqFkMtOwkAUhidGI4gufAHTnXFROHNpZ2YpRC6ClwXGxM1k2k6hWCh22iBvb6XAzrg65yTf_5_kQ-gaQxsDkM4iDNqEMIFPUBOD5C7zGTtFTeAUXEIxaaALaxcAICUl56hBAAShhDbR5FUX8yzNZltHryInSPa7tVmY6MJEziYp5k4xN06c61mSGqc_HE2dmVmZXWK3rPMsKsPiEp3FOrXmaj9b6K3_MO0N3cnLYNS7n7ghlQy7MdNaSoKBEiwEY4J5AjjzPB4ST3IjDLCAEA44jqtb-jKKAgq-F1MsKQPaQrd1b_X3qzS2UMvEhiZN9cpkpVXSF9j3mMf_JTmljPmc-BV5V5Nhnlmbm1it82Sp863CoH4tq8qy2lmu2Jt9axksTXQkD1oroFMDm0rY9u8m9djrHirdOpHYwnwfEzr_VD6n3FPvzwPV_RiDGJAnNaY_7j-RtQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>733446726</pqid></control><display><type>article</type><title>Pathology and biology associated with the fragile FHIT gene and gene product</title><source>MEDLINE</source><source>Wiley Online Library</source><creator>Saldivar, Joshua C. ; Shibata, Hidetaka ; Huebner, Kay</creator><creatorcontrib>Saldivar, Joshua C. ; Shibata, Hidetaka ; Huebner, Kay</creatorcontrib><description>More than 12 years and >800 scientific publications after the discovery of the first gene at a chromosome fragile site, the FHIT gene at FRA3B, there are still questions to pursue concerning the selective advantage conferred to cells by loss of expression of FHIT, the most frequent target of allele deletion in precancerous lesions and cancers. These questions are considered in light of recent investigations of genetic and epigenetic alterations to the locus and in a retrospective consideration of biological roles of the Fhit protein discovered through functional studies. J. Cell. Biochem. 109: 858–865, 2010. © 2010 Wiley‐Liss, Inc.</description><identifier>ISSN: 0730-2312</identifier><identifier>ISSN: 1097-4644</identifier><identifier>EISSN: 1097-4644</identifier><identifier>DOI: 10.1002/jcb.22481</identifier><identifier>PMID: 20082323</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Acid Anhydride Hydrolases - genetics ; Acid Anhydride Hydrolases - metabolism ; Animals ; common fragile sites ; DNA damage checkpoint ; DNA repair ; FHIT ; Gene Expression Regulation, Neoplastic ; Humans ; Neoplasm Proteins - genetics ; Neoplasm Proteins - metabolism ; Neoplasms - genetics ; Neoplasms - pathology ; promoter methylation</subject><ispartof>Journal of cellular biochemistry, 2010-04, Vol.109 (5), p.858-865</ispartof><rights>Copyright © 2010 Wiley‐Liss, Inc.</rights><rights>Copyright 2010 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3941-f4aa9921032188448458074557c2597e8e04b22701ff597969ddb3065f3193403</citedby><cites>FETCH-LOGICAL-c3941-f4aa9921032188448458074557c2597e8e04b22701ff597969ddb3065f3193403</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjcb.22481$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjcb.22481$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20082323$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saldivar, Joshua C.</creatorcontrib><creatorcontrib>Shibata, Hidetaka</creatorcontrib><creatorcontrib>Huebner, Kay</creatorcontrib><title>Pathology and biology associated with the fragile FHIT gene and gene product</title><title>Journal of cellular biochemistry</title><addtitle>J. Cell. Biochem</addtitle><description>More than 12 years and >800 scientific publications after the discovery of the first gene at a chromosome fragile site, the FHIT gene at FRA3B, there are still questions to pursue concerning the selective advantage conferred to cells by loss of expression of FHIT, the most frequent target of allele deletion in precancerous lesions and cancers. These questions are considered in light of recent investigations of genetic and epigenetic alterations to the locus and in a retrospective consideration of biological roles of the Fhit protein discovered through functional studies. J. Cell. Biochem. 109: 858–865, 2010. © 2010 Wiley‐Liss, Inc.</description><subject>Acid Anhydride Hydrolases - genetics</subject><subject>Acid Anhydride Hydrolases - metabolism</subject><subject>Animals</subject><subject>common fragile sites</subject><subject>DNA damage checkpoint</subject><subject>DNA repair</subject><subject>FHIT</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Neoplasm Proteins - genetics</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Neoplasms - genetics</subject><subject>Neoplasms - pathology</subject><subject>promoter methylation</subject><issn>0730-2312</issn><issn>1097-4644</issn><issn>1097-4644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOwkAUhidGI4gufAHTnXFROHNpZ2YpRC6ClwXGxM1k2k6hWCh22iBvb6XAzrg65yTf_5_kQ-gaQxsDkM4iDNqEMIFPUBOD5C7zGTtFTeAUXEIxaaALaxcAICUl56hBAAShhDbR5FUX8yzNZltHryInSPa7tVmY6MJEziYp5k4xN06c61mSGqc_HE2dmVmZXWK3rPMsKsPiEp3FOrXmaj9b6K3_MO0N3cnLYNS7n7ghlQy7MdNaSoKBEiwEY4J5AjjzPB4ST3IjDLCAEA44jqtb-jKKAgq-F1MsKQPaQrd1b_X3qzS2UMvEhiZN9cpkpVXSF9j3mMf_JTmljPmc-BV5V5Nhnlmbm1it82Sp863CoH4tq8qy2lmu2Jt9axksTXQkD1oroFMDm0rY9u8m9djrHirdOpHYwnwfEzr_VD6n3FPvzwPV_RiDGJAnNaY_7j-RtQ</recordid><startdate>20100401</startdate><enddate>20100401</enddate><creator>Saldivar, Joshua C.</creator><creator>Shibata, Hidetaka</creator><creator>Huebner, Kay</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20100401</creationdate><title>Pathology and biology associated with the fragile FHIT gene and gene product</title><author>Saldivar, Joshua C. ; Shibata, Hidetaka ; Huebner, Kay</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3941-f4aa9921032188448458074557c2597e8e04b22701ff597969ddb3065f3193403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acid Anhydride Hydrolases - genetics</topic><topic>Acid Anhydride Hydrolases - metabolism</topic><topic>Animals</topic><topic>common fragile sites</topic><topic>DNA damage checkpoint</topic><topic>DNA repair</topic><topic>FHIT</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Neoplasm Proteins - genetics</topic><topic>Neoplasm Proteins - metabolism</topic><topic>Neoplasms - genetics</topic><topic>Neoplasms - pathology</topic><topic>promoter methylation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saldivar, Joshua C.</creatorcontrib><creatorcontrib>Shibata, Hidetaka</creatorcontrib><creatorcontrib>Huebner, Kay</creatorcontrib><collection>Istex</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Journal of cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saldivar, Joshua C.</au><au>Shibata, Hidetaka</au><au>Huebner, Kay</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pathology and biology associated with the fragile FHIT gene and gene product</atitle><jtitle>Journal of cellular biochemistry</jtitle><addtitle>J. Cell. Biochem</addtitle><date>2010-04-01</date><risdate>2010</risdate><volume>109</volume><issue>5</issue><spage>858</spage><epage>865</epage><pages>858-865</pages><issn>0730-2312</issn><issn>1097-4644</issn><eissn>1097-4644</eissn><abstract>More than 12 years and >800 scientific publications after the discovery of the first gene at a chromosome fragile site, the FHIT gene at FRA3B, there are still questions to pursue concerning the selective advantage conferred to cells by loss of expression of FHIT, the most frequent target of allele deletion in precancerous lesions and cancers. These questions are considered in light of recent investigations of genetic and epigenetic alterations to the locus and in a retrospective consideration of biological roles of the Fhit protein discovered through functional studies. J. Cell. Biochem. 109: 858–865, 2010. © 2010 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>20082323</pmid><doi>10.1002/jcb.22481</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0730-2312 |
ispartof | Journal of cellular biochemistry, 2010-04, Vol.109 (5), p.858-865 |
issn | 0730-2312 1097-4644 1097-4644 |
language | eng |
recordid | cdi_proquest_miscellaneous_968165457 |
source | MEDLINE; Wiley Online Library |
subjects | Acid Anhydride Hydrolases - genetics Acid Anhydride Hydrolases - metabolism Animals common fragile sites DNA damage checkpoint DNA repair FHIT Gene Expression Regulation, Neoplastic Humans Neoplasm Proteins - genetics Neoplasm Proteins - metabolism Neoplasms - genetics Neoplasms - pathology promoter methylation |
title | Pathology and biology associated with the fragile FHIT gene and gene product |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T10%3A36%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pathology%20and%20biology%20associated%20with%20the%20fragile%20FHIT%20gene%20and%20gene%20product&rft.jtitle=Journal%20of%20cellular%20biochemistry&rft.au=Saldivar,%20Joshua%20C.&rft.date=2010-04-01&rft.volume=109&rft.issue=5&rft.spage=858&rft.epage=865&rft.pages=858-865&rft.issn=0730-2312&rft.eissn=1097-4644&rft_id=info:doi/10.1002/jcb.22481&rft_dat=%3Cproquest_cross%3E968165457%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=733446726&rft_id=info:pmid/20082323&rfr_iscdi=true |