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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of cellular biochemistry 2010-04, Vol.109 (5), p.858-865
Hauptverfasser: Saldivar, Joshua C., Shibata, Hidetaka, Huebner, Kay
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 &gt;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 &gt;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 &gt;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