Roles for KRAS in Pancreatic Tumor Development and Progression
The Kras gene is mutated to an oncogenic form in most pancreatic tumors. However, early attempts to use this molecule as a specific biomarker of the disease, or inhibit its activity as a cancer therapy, failed. This left a situation in which everyone was aware of the association between this importa...
Gespeichert in:
Veröffentlicht in: | Gastroenterology (New York, N.Y. 1943) N.Y. 1943), 2013-06, Vol.144 (6), p.1220-1229 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1229 |
---|---|
container_issue | 6 |
container_start_page | 1220 |
container_title | Gastroenterology (New York, N.Y. 1943) |
container_volume | 144 |
creator | di Magliano, Marina Pasca Logsdon, Craig D |
description | The Kras gene is mutated to an oncogenic form in most pancreatic tumors. However, early attempts to use this molecule as a specific biomarker of the disease, or inhibit its activity as a cancer therapy, failed. This left a situation in which everyone was aware of the association between this important oncogene and pancreatic cancer, but no one knew what to do about it. Recent findings have changed this picture—many assumptions made about KRAS and its role in pancreatic cancer were found to be incorrect. Several factors have contributed to increased understanding of the activities of KRAS, including creation of genetically engineered mouse models, which have allowed for detailed analyses of pancreatic carcinogenesis in an intact animal with a competent immune system. Cancer genome sequencing projects have increased our understanding of the heterogeneity of individual tumors. We also have a better understanding of which oncogenes are important for tumor maintenance and are therefore called “drivers.” We review the advances and limitations of our knowledge about the role of Kras in development of pancreatic cancers and the important areas for future research. |
doi_str_mv | 10.1053/j.gastro.2013.01.071 |
format | Article |
fullrecord | <record><control><sourceid>elsevier_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3902845</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0016508513001911</els_id><sourcerecordid>S0016508513001911</sourcerecordid><originalsourceid>FETCH-LOGICAL-c584t-4e676797ee812dcee581bf98219e2873851e7d6607c2fdf3ef7efea2cc3236973</originalsourceid><addsrcrecordid>eNqFkdtO3DAQhq2qqGyhb4CqvEBSj72JnRskRKFFIIE4XI-MM1m8zdorO7sSb49Xy6Fww9VYGv3fjL9h7AB4BbyWv-bVzKQxhkpwkBWHiiv4wiZQC11yDuIrm-TSlDXX9S77ntKcc95KDd_YrpCNECBhwg6vw0Cp6EMszq-PbgrniyvjbSQzOlvcrha58ZvWNITlgvxYGN8VVzHMIqXkgt9nO70ZEv14rnvs7vTk9vhveXH55-z46KK0tZ6O5ZQa1ahWEWkQnSWqNdz3rRbQktBK6hpIdU3DlRV910vqFfVkhLUyr9oquccOt9zl6n5BmeDHaAZcRrcw8RGDcfi-490DzsIaZcuFntYZMN0CbAwpRepfs8Bx4xPnuPWJG5_IAbPPHPv5_9zX0IvAt8Uo_37tKGKyjrylzkWyI3bBfTbhI8AOzjtrhn_0SGkeVtFnswiYBHK82dx0c1KQ-dUCyCeJB55A</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Roles for KRAS in Pancreatic Tumor Development and Progression</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><source>Alma/SFX Local Collection</source><creator>di Magliano, Marina Pasca ; Logsdon, Craig D</creator><creatorcontrib>di Magliano, Marina Pasca ; Logsdon, Craig D</creatorcontrib><description>The Kras gene is mutated to an oncogenic form in most pancreatic tumors. However, early attempts to use this molecule as a specific biomarker of the disease, or inhibit its activity as a cancer therapy, failed. This left a situation in which everyone was aware of the association between this important oncogene and pancreatic cancer, but no one knew what to do about it. Recent findings have changed this picture—many assumptions made about KRAS and its role in pancreatic cancer were found to be incorrect. Several factors have contributed to increased understanding of the activities of KRAS, including creation of genetically engineered mouse models, which have allowed for detailed analyses of pancreatic carcinogenesis in an intact animal with a competent immune system. Cancer genome sequencing projects have increased our understanding of the heterogeneity of individual tumors. We also have a better understanding of which oncogenes are important for tumor maintenance and are therefore called “drivers.” We review the advances and limitations of our knowledge about the role of Kras in development of pancreatic cancers and the important areas for future research.</description><identifier>ISSN: 0016-5085</identifier><identifier>EISSN: 1528-0012</identifier><identifier>DOI: 10.1053/j.gastro.2013.01.071</identifier><identifier>PMID: 23622131</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Cell Transformation, Neoplastic - genetics ; Cell Transformation, Neoplastic - metabolism ; Cell Transformation, Neoplastic - pathology ; Disease Progression ; Gastroenterology and Hepatology ; Gene Expression Regulation, Neoplastic ; Genetic Predisposition to Disease ; Humans ; Inflammation ; Kras ; Mouse Model ; Mutation ; Pancreatic Cancer ; Pancreatic Neoplasms - genetics ; Pancreatic Neoplasms - metabolism ; Pancreatic Neoplasms - pathology ; Pancreatic Neoplasms - therapy ; Phenotype ; Prognosis ; Proto-Oncogene Proteins - genetics ; Proto-Oncogene Proteins - metabolism ; Proto-Oncogene Proteins p21(ras) ; ras Proteins - genetics ; ras Proteins - metabolism ; Signal Transduction</subject><ispartof>Gastroenterology (New York, N.Y. 1943), 2013-06, Vol.144 (6), p.1220-1229</ispartof><rights>AGA Institute</rights><rights>2013 AGA Institute</rights><rights>Copyright © 2013 AGA Institute. Published by Elsevier Inc. All rights reserved.</rights><rights>2013 by the AGA Institute 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c584t-4e676797ee812dcee581bf98219e2873851e7d6607c2fdf3ef7efea2cc3236973</citedby><cites>FETCH-LOGICAL-c584t-4e676797ee812dcee581bf98219e2873851e7d6607c2fdf3ef7efea2cc3236973</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1053/j.gastro.2013.01.071$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23622131$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>di Magliano, Marina Pasca</creatorcontrib><creatorcontrib>Logsdon, Craig D</creatorcontrib><title>Roles for KRAS in Pancreatic Tumor Development and Progression</title><title>Gastroenterology (New York, N.Y. 1943)</title><addtitle>Gastroenterology</addtitle><description>The Kras gene is mutated to an oncogenic form in most pancreatic tumors. However, early attempts to use this molecule as a specific biomarker of the disease, or inhibit its activity as a cancer therapy, failed. This left a situation in which everyone was aware of the association between this important oncogene and pancreatic cancer, but no one knew what to do about it. Recent findings have changed this picture—many assumptions made about KRAS and its role in pancreatic cancer were found to be incorrect. Several factors have contributed to increased understanding of the activities of KRAS, including creation of genetically engineered mouse models, which have allowed for detailed analyses of pancreatic carcinogenesis in an intact animal with a competent immune system. Cancer genome sequencing projects have increased our understanding of the heterogeneity of individual tumors. We also have a better understanding of which oncogenes are important for tumor maintenance and are therefore called “drivers.” We review the advances and limitations of our knowledge about the role of Kras in development of pancreatic cancers and the important areas for future research.</description><subject>Animals</subject><subject>Cell Transformation, Neoplastic - genetics</subject><subject>Cell Transformation, Neoplastic - metabolism</subject><subject>Cell Transformation, Neoplastic - pathology</subject><subject>Disease Progression</subject><subject>Gastroenterology and Hepatology</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Genetic Predisposition to Disease</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Kras</subject><subject>Mouse Model</subject><subject>Mutation</subject><subject>Pancreatic Cancer</subject><subject>Pancreatic Neoplasms - genetics</subject><subject>Pancreatic Neoplasms - metabolism</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Pancreatic Neoplasms - therapy</subject><subject>Phenotype</subject><subject>Prognosis</subject><subject>Proto-Oncogene Proteins - genetics</subject><subject>Proto-Oncogene Proteins - metabolism</subject><subject>Proto-Oncogene Proteins p21(ras)</subject><subject>ras Proteins - genetics</subject><subject>ras Proteins - metabolism</subject><subject>Signal Transduction</subject><issn>0016-5085</issn><issn>1528-0012</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkdtO3DAQhq2qqGyhb4CqvEBSj72JnRskRKFFIIE4XI-MM1m8zdorO7sSb49Xy6Fww9VYGv3fjL9h7AB4BbyWv-bVzKQxhkpwkBWHiiv4wiZQC11yDuIrm-TSlDXX9S77ntKcc95KDd_YrpCNECBhwg6vw0Cp6EMszq-PbgrniyvjbSQzOlvcrha58ZvWNITlgvxYGN8VVzHMIqXkgt9nO70ZEv14rnvs7vTk9vhveXH55-z46KK0tZ6O5ZQa1ahWEWkQnSWqNdz3rRbQktBK6hpIdU3DlRV910vqFfVkhLUyr9oquccOt9zl6n5BmeDHaAZcRrcw8RGDcfi-490DzsIaZcuFntYZMN0CbAwpRepfs8Bx4xPnuPWJG5_IAbPPHPv5_9zX0IvAt8Uo_37tKGKyjrylzkWyI3bBfTbhI8AOzjtrhn_0SGkeVtFnswiYBHK82dx0c1KQ-dUCyCeJB55A</recordid><startdate>20130601</startdate><enddate>20130601</enddate><creator>di Magliano, Marina Pasca</creator><creator>Logsdon, Craig D</creator><general>Elsevier Inc</general><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>5PM</scope></search><sort><creationdate>20130601</creationdate><title>Roles for KRAS in Pancreatic Tumor Development and Progression</title><author>di Magliano, Marina Pasca ; Logsdon, Craig D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c584t-4e676797ee812dcee581bf98219e2873851e7d6607c2fdf3ef7efea2cc3236973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Cell Transformation, Neoplastic - genetics</topic><topic>Cell Transformation, Neoplastic - metabolism</topic><topic>Cell Transformation, Neoplastic - pathology</topic><topic>Disease Progression</topic><topic>Gastroenterology and Hepatology</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Genetic Predisposition to Disease</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Kras</topic><topic>Mouse Model</topic><topic>Mutation</topic><topic>Pancreatic Cancer</topic><topic>Pancreatic Neoplasms - genetics</topic><topic>Pancreatic Neoplasms - metabolism</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Pancreatic Neoplasms - therapy</topic><topic>Phenotype</topic><topic>Prognosis</topic><topic>Proto-Oncogene Proteins - genetics</topic><topic>Proto-Oncogene Proteins - metabolism</topic><topic>Proto-Oncogene Proteins p21(ras)</topic><topic>ras Proteins - genetics</topic><topic>ras Proteins - metabolism</topic><topic>Signal Transduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>di Magliano, Marina Pasca</creatorcontrib><creatorcontrib>Logsdon, Craig D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Gastroenterology (New York, N.Y. 1943)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>di Magliano, Marina Pasca</au><au>Logsdon, Craig D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Roles for KRAS in Pancreatic Tumor Development and Progression</atitle><jtitle>Gastroenterology (New York, N.Y. 1943)</jtitle><addtitle>Gastroenterology</addtitle><date>2013-06-01</date><risdate>2013</risdate><volume>144</volume><issue>6</issue><spage>1220</spage><epage>1229</epage><pages>1220-1229</pages><issn>0016-5085</issn><eissn>1528-0012</eissn><abstract>The Kras gene is mutated to an oncogenic form in most pancreatic tumors. However, early attempts to use this molecule as a specific biomarker of the disease, or inhibit its activity as a cancer therapy, failed. This left a situation in which everyone was aware of the association between this important oncogene and pancreatic cancer, but no one knew what to do about it. Recent findings have changed this picture—many assumptions made about KRAS and its role in pancreatic cancer were found to be incorrect. Several factors have contributed to increased understanding of the activities of KRAS, including creation of genetically engineered mouse models, which have allowed for detailed analyses of pancreatic carcinogenesis in an intact animal with a competent immune system. Cancer genome sequencing projects have increased our understanding of the heterogeneity of individual tumors. We also have a better understanding of which oncogenes are important for tumor maintenance and are therefore called “drivers.” We review the advances and limitations of our knowledge about the role of Kras in development of pancreatic cancers and the important areas for future research.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>23622131</pmid><doi>10.1053/j.gastro.2013.01.071</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0016-5085 |
ispartof | Gastroenterology (New York, N.Y. 1943), 2013-06, Vol.144 (6), p.1220-1229 |
issn | 0016-5085 1528-0012 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3902845 |
source | MEDLINE; Elsevier ScienceDirect Journals; Alma/SFX Local Collection |
subjects | Animals Cell Transformation, Neoplastic - genetics Cell Transformation, Neoplastic - metabolism Cell Transformation, Neoplastic - pathology Disease Progression Gastroenterology and Hepatology Gene Expression Regulation, Neoplastic Genetic Predisposition to Disease Humans Inflammation Kras Mouse Model Mutation Pancreatic Cancer Pancreatic Neoplasms - genetics Pancreatic Neoplasms - metabolism Pancreatic Neoplasms - pathology Pancreatic Neoplasms - therapy Phenotype Prognosis Proto-Oncogene Proteins - genetics Proto-Oncogene Proteins - metabolism Proto-Oncogene Proteins p21(ras) ras Proteins - genetics ras Proteins - metabolism Signal Transduction |
title | Roles for KRAS in Pancreatic Tumor Development and Progression |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T17%3A54%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Roles%20for%20KRAS%20in%20Pancreatic%20Tumor%20Development%20and%20Progression&rft.jtitle=Gastroenterology%20(New%20York,%20N.Y.%201943)&rft.au=di%20Magliano,%20Marina%20Pasca&rft.date=2013-06-01&rft.volume=144&rft.issue=6&rft.spage=1220&rft.epage=1229&rft.pages=1220-1229&rft.issn=0016-5085&rft.eissn=1528-0012&rft_id=info:doi/10.1053/j.gastro.2013.01.071&rft_dat=%3Celsevier_pubme%3ES0016508513001911%3C/elsevier_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/23622131&rft_els_id=S0016508513001911&rfr_iscdi=true |