Simultaneous mutations in K-ras and TP53 are indicative of poor prognosis in sporadic colorectal cancer
Despite the fact that the mutations in K-ras codon 12 and TP53 are common abnormalities in colorectal cancer, the determination of K-ras mutation combined with TP53 gene mutation, with diagnostic and prognostic purposes is still controversial. We have analyzed K-ras and TP53 mutations in 77 sporadic...
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Veröffentlicht in: | American journal of clinical oncology 2004-02, Vol.27 (1), p.39-45 |
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creator | González-Aguilera, Juan J Oliart, Soledad Azcoita, Mariano Moreno Fernández-Peralta, Antonia M |
description | Despite the fact that the mutations in K-ras codon 12 and TP53 are common abnormalities in colorectal cancer, the determination of K-ras mutation combined with TP53 gene mutation, with diagnostic and prognostic purposes is still controversial. We have analyzed K-ras and TP53 mutations in 77 sporadic colorectal adenocarcinomas by means of polymerase chain reaction and sequencing. We observed a negative correlation between both K-ras and TP53 mutations. Patients with mutations in K-ras but not in TP53 exhibited worse survival rates than those with mutations in TP53 and not in K-ras. Moreover, we found the worst outcome in patients with mutations in both K-ras and TP53. These results may relate to the previously published data about primary human and rodent cells, in which transformation by Ras require either a cooperating oncogene or the inactivation of tumor suppressors such as p53 or p16. In conclusion, simultaneous mutations in K-ras and TP53 are indicative of a worse prognosis in sporadic colorectal cancer. |
doi_str_mv | 10.1097/01.coc.0000045920.49210.7A |
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We have analyzed K-ras and TP53 mutations in 77 sporadic colorectal adenocarcinomas by means of polymerase chain reaction and sequencing. We observed a negative correlation between both K-ras and TP53 mutations. Patients with mutations in K-ras but not in TP53 exhibited worse survival rates than those with mutations in TP53 and not in K-ras. Moreover, we found the worst outcome in patients with mutations in both K-ras and TP53. These results may relate to the previously published data about primary human and rodent cells, in which transformation by Ras require either a cooperating oncogene or the inactivation of tumor suppressors such as p53 or p16. 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We have analyzed K-ras and TP53 mutations in 77 sporadic colorectal adenocarcinomas by means of polymerase chain reaction and sequencing. We observed a negative correlation between both K-ras and TP53 mutations. Patients with mutations in K-ras but not in TP53 exhibited worse survival rates than those with mutations in TP53 and not in K-ras. Moreover, we found the worst outcome in patients with mutations in both K-ras and TP53. These results may relate to the previously published data about primary human and rodent cells, in which transformation by Ras require either a cooperating oncogene or the inactivation of tumor suppressors such as p53 or p16. In conclusion, simultaneous mutations in K-ras and TP53 are indicative of a worse prognosis in sporadic colorectal cancer.</description><subject>Adenocarcinoma - genetics</subject><subject>Adenocarcinoma - mortality</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - mortality</subject><subject>Female</subject><subject>Genes, p53 - genetics</subject><subject>Genes, ras - genetics</subject><subject>Humans</subject><subject>Loss of Heterozygosity</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Prognosis</subject><issn>0277-3732</issn><issn>1537-453X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkF1PwyAUhonRuDn9C4Z44V0rB0oZ3i2LX3GJJs7EO0IpXWraUqE18d_LPpKdG07geQ_wIHQDJAUixR2B1DiTkm1lXFKSZpLGQ7E4QVPgTCQZZ1-naEqoEAkTjE7QRQjfEec5EedoApngc2B0ijYfdTs2g-6sGwNux0EPtesCrjv8mngdsO5KvH7nDGtv425Zm0j8Wuwq3Dvnce_dpnOh3kVC77yOCDaucd6aQTfY6M5Yf4nOKt0Ee3VYZ-jz8WG9fE5Wb08vy8UqMQz4kDAm87IgnJasEFBZoEaKEvLYakIKKwsKgnIhSgIF1eVc5DmjhpKC0ExyyWbodj83vutntGFQbR2MbZr9D9WcAM0h24L3e9B4F4K3lep93Wr_p4CorWZFQEXN6qhZ7TQrsYjh68MtY9Ha8hg9eGX_exd50g</recordid><startdate>200402</startdate><enddate>200402</enddate><creator>González-Aguilera, Juan J</creator><creator>Oliart, Soledad</creator><creator>Azcoita, Mariano Moreno</creator><creator>Fernández-Peralta, Antonia M</creator><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></search><sort><creationdate>200402</creationdate><title>Simultaneous mutations in K-ras and TP53 are indicative of poor prognosis in sporadic colorectal cancer</title><author>González-Aguilera, Juan J ; Oliart, Soledad ; Azcoita, Mariano Moreno ; Fernández-Peralta, Antonia M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c315t-3396db052d3b71fe12c97d161fea00be9b2172577d01b2ad876632c20b0249593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adenocarcinoma - genetics</topic><topic>Adenocarcinoma - mortality</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - mortality</topic><topic>Female</topic><topic>Genes, p53 - genetics</topic><topic>Genes, ras - genetics</topic><topic>Humans</topic><topic>Loss of Heterozygosity</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Prognosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>González-Aguilera, Juan J</creatorcontrib><creatorcontrib>Oliart, Soledad</creatorcontrib><creatorcontrib>Azcoita, Mariano Moreno</creatorcontrib><creatorcontrib>Fernández-Peralta, Antonia M</creatorcontrib><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><jtitle>American journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>González-Aguilera, Juan J</au><au>Oliart, Soledad</au><au>Azcoita, Mariano Moreno</au><au>Fernández-Peralta, Antonia M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous mutations in K-ras and TP53 are indicative of poor prognosis in sporadic colorectal cancer</atitle><jtitle>American journal of clinical oncology</jtitle><addtitle>Am J Clin Oncol</addtitle><date>2004-02</date><risdate>2004</risdate><volume>27</volume><issue>1</issue><spage>39</spage><epage>45</epage><pages>39-45</pages><issn>0277-3732</issn><eissn>1537-453X</eissn><abstract>Despite the fact that the mutations in K-ras codon 12 and TP53 are common abnormalities in colorectal cancer, the determination of K-ras mutation combined with TP53 gene mutation, with diagnostic and prognostic purposes is still controversial. We have analyzed K-ras and TP53 mutations in 77 sporadic colorectal adenocarcinomas by means of polymerase chain reaction and sequencing. We observed a negative correlation between both K-ras and TP53 mutations. Patients with mutations in K-ras but not in TP53 exhibited worse survival rates than those with mutations in TP53 and not in K-ras. Moreover, we found the worst outcome in patients with mutations in both K-ras and TP53. These results may relate to the previously published data about primary human and rodent cells, in which transformation by Ras require either a cooperating oncogene or the inactivation of tumor suppressors such as p53 or p16. In conclusion, simultaneous mutations in K-ras and TP53 are indicative of a worse prognosis in sporadic colorectal cancer.</abstract><cop>United States</cop><pmid>14758132</pmid><doi>10.1097/01.coc.0000045920.49210.7A</doi><tpages>7</tpages></addata></record> |
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subjects | Adenocarcinoma - genetics Adenocarcinoma - mortality Adolescent Adult Aged Aged, 80 and over Colorectal Neoplasms - genetics Colorectal Neoplasms - mortality Female Genes, p53 - genetics Genes, ras - genetics Humans Loss of Heterozygosity Male Middle Aged Mutation Prognosis |
title | Simultaneous mutations in K-ras and TP53 are indicative of poor prognosis in sporadic colorectal cancer |
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