Novel recurrently mutated genes in African American colon cancers
Significance Colorectal cancer is a leading cause of cancer-related deaths world-wide. African Americans exhibit the highest colon cancer incidence and mortality among all ethnic groups in the United States. Despite this finding, there is a dearth of knowledge on the genetic mechanisms underlying co...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2015-01, Vol.112 (4), p.1149-1154 |
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creator | Guda, Kishore Veigl, Martina L. Varadan, Vinay Nosrati, Arman Ravi, Lakshmeswari Lutterbaugh, James Beard, Lydia Willson, James K. V. Sedwick, W. David Wang, Zhenghe John Molyneaux, Neil Miron, Alexander Adams, Mark D. Elston, Robert C. Markowitz, Sanford D. Willis, Joseph E. |
description | Significance Colorectal cancer is a leading cause of cancer-related deaths world-wide. African Americans exhibit the highest colon cancer incidence and mortality among all ethnic groups in the United States. Despite this finding, there is a dearth of knowledge on the genetic mechanisms underlying colon carcinogenesis in African Americans. We thus initiated this study to characterize the mutational landscapes of African American colon cancers. We identified new genes that are significantly mutated in colon cancer and that are highly preferentially targeted for mutations in colon cancers arising in African Americans as compared with Caucasians. These findings suggest differences in routes of colon carcinogenesis between the different ethnic groups and also may have implications for the ethnicity associated differences in tumor incidence and outcome.
We used whole-exome and targeted sequencing to characterize somatic mutations in 103 colorectal cancers (CRC) from African Americans, identifying 20 new genes as significantly mutated in CRC. Resequencing 129 Caucasian derived CRCs confirmed a 15-gene set as a preferential target for mutations in African American CRCs. Two predominant genes, ephrin type A receptor 6 ( EPHA6 ) and folliculin ( FLCN ), with mutations exclusive to African American CRCs, are by genetic and biological criteria highly likely African American CRC driver genes. These previously unsuspected differences in the mutational landscapes of CRCs arising among individuals of different ethnicities have potential to impact on broader disparities in cancer behaviors. |
doi_str_mv | 10.1073/pnas.1417064112 |
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We used whole-exome and targeted sequencing to characterize somatic mutations in 103 colorectal cancers (CRC) from African Americans, identifying 20 new genes as significantly mutated in CRC. Resequencing 129 Caucasian derived CRCs confirmed a 15-gene set as a preferential target for mutations in African American CRCs. Two predominant genes, ephrin type A receptor 6 ( EPHA6 ) and folliculin ( FLCN ), with mutations exclusive to African American CRCs, are by genetic and biological criteria highly likely African American CRC driver genes. These previously unsuspected differences in the mutational landscapes of CRCs arising among individuals of different ethnicities have potential to impact on broader disparities in cancer behaviors.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1417064112</identifier><identifier>PMID: 25583493</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>African Americans ; African Americans - genetics ; Biological Sciences ; carcinogenesis ; colon ; Colonic Neoplasms - ethnology ; Colonic Neoplasms - genetics ; Colorectal cancer ; colorectal neoplasms ; European Continental Ancestry Group - genetics ; Exome ; Female ; Genes ; Genetics ; Genome-Wide Association Study ; Health behavior ; Humans ; Male ; mortality ; Mutation ; Proto-Oncogene Proteins - genetics ; Receptor, EphA6 - genetics ; Tumor Suppressor Proteins - genetics ; United States ; Whites</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2015-01, Vol.112 (4), p.1149-1154</ispartof><rights>Volumes 1–89 and 106–112, copyright as a collective work only; author(s) retains copyright to individual articles</rights><rights>Copyright National Academy of Sciences Jan 27, 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c556t-74ef847223ee5c6089dbed2e00a342a08508102dc73e45cd6a8eb474cf8042523</citedby><cites>FETCH-LOGICAL-c556t-74ef847223ee5c6089dbed2e00a342a08508102dc73e45cd6a8eb474cf8042523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/112/4.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/26454247$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/26454247$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27901,27902,53766,53768,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25583493$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guda, Kishore</creatorcontrib><creatorcontrib>Veigl, Martina L.</creatorcontrib><creatorcontrib>Varadan, Vinay</creatorcontrib><creatorcontrib>Nosrati, Arman</creatorcontrib><creatorcontrib>Ravi, Lakshmeswari</creatorcontrib><creatorcontrib>Lutterbaugh, James</creatorcontrib><creatorcontrib>Beard, Lydia</creatorcontrib><creatorcontrib>Willson, James K. V.</creatorcontrib><creatorcontrib>Sedwick, W. David</creatorcontrib><creatorcontrib>Wang, Zhenghe John</creatorcontrib><creatorcontrib>Molyneaux, Neil</creatorcontrib><creatorcontrib>Miron, Alexander</creatorcontrib><creatorcontrib>Adams, Mark D.</creatorcontrib><creatorcontrib>Elston, Robert C.</creatorcontrib><creatorcontrib>Markowitz, Sanford D.</creatorcontrib><creatorcontrib>Willis, Joseph E.</creatorcontrib><title>Novel recurrently mutated genes in African American colon cancers</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Significance Colorectal cancer is a leading cause of cancer-related deaths world-wide. African Americans exhibit the highest colon cancer incidence and mortality among all ethnic groups in the United States. Despite this finding, there is a dearth of knowledge on the genetic mechanisms underlying colon carcinogenesis in African Americans. We thus initiated this study to characterize the mutational landscapes of African American colon cancers. We identified new genes that are significantly mutated in colon cancer and that are highly preferentially targeted for mutations in colon cancers arising in African Americans as compared with Caucasians. These findings suggest differences in routes of colon carcinogenesis between the different ethnic groups and also may have implications for the ethnicity associated differences in tumor incidence and outcome.
We used whole-exome and targeted sequencing to characterize somatic mutations in 103 colorectal cancers (CRC) from African Americans, identifying 20 new genes as significantly mutated in CRC. Resequencing 129 Caucasian derived CRCs confirmed a 15-gene set as a preferential target for mutations in African American CRCs. Two predominant genes, ephrin type A receptor 6 ( EPHA6 ) and folliculin ( FLCN ), with mutations exclusive to African American CRCs, are by genetic and biological criteria highly likely African American CRC driver genes. These previously unsuspected differences in the mutational landscapes of CRCs arising among individuals of different ethnicities have potential to impact on broader disparities in cancer behaviors.</description><subject>African Americans</subject><subject>African Americans - genetics</subject><subject>Biological Sciences</subject><subject>carcinogenesis</subject><subject>colon</subject><subject>Colonic Neoplasms - ethnology</subject><subject>Colonic Neoplasms - genetics</subject><subject>Colorectal cancer</subject><subject>colorectal neoplasms</subject><subject>European Continental Ancestry Group - genetics</subject><subject>Exome</subject><subject>Female</subject><subject>Genes</subject><subject>Genetics</subject><subject>Genome-Wide Association Study</subject><subject>Health behavior</subject><subject>Humans</subject><subject>Male</subject><subject>mortality</subject><subject>Mutation</subject><subject>Proto-Oncogene Proteins - genetics</subject><subject>Receptor, EphA6 - genetics</subject><subject>Tumor Suppressor Proteins - genetics</subject><subject>United States</subject><subject>Whites</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkkFv1DAQhS0EotuFMycgEhcuacf22HEuSKuKAlIFB-jZ8jqTJatsvNhJpf57vKRsCxe4zFiab55m5pmxFxzOOFTyfD-4dMaRV6CRc_GILTjUvNRYw2O2ABBVaVDgCTtNaQsAtTLwlJ0IpYzEWi7Y6nO4ob6I5KcYaRj722I3jW6kptjQQKnohmLVxs67nHc0P3zoQ45u8BTTM_akdX2i53d5ya4v33-7-Fheffnw6WJ1VXql9FhWSK3BSghJpLwGUzdragQBOInCgVFgOIjGV5JQ-UY7Q2us0LcGUCghl-zdrLuf1jtqfB42ut7uY7dz8dYG19k_K0P33W7CjUXJpdGQBd7eCcTwY6I02l2XPPW9GyhMyXIDEkweUP8b1doIVLX6D1WtBHKjf6m--QvdhikO-WgHKjtoNMdMnc-UjyGlSO1xRQ72YLo9mG7vTc8drx5e5sj_dvkBcOg8ynFhMcdMLNnLGdimMcR7AY0q_54q11_P9dYF6zaxS_b6qwCuAXg-A2r5E4wSwxw</recordid><startdate>20150127</startdate><enddate>20150127</enddate><creator>Guda, Kishore</creator><creator>Veigl, Martina L.</creator><creator>Varadan, Vinay</creator><creator>Nosrati, Arman</creator><creator>Ravi, Lakshmeswari</creator><creator>Lutterbaugh, James</creator><creator>Beard, Lydia</creator><creator>Willson, James K. 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V.</au><au>Sedwick, W. David</au><au>Wang, Zhenghe John</au><au>Molyneaux, Neil</au><au>Miron, Alexander</au><au>Adams, Mark D.</au><au>Elston, Robert C.</au><au>Markowitz, Sanford D.</au><au>Willis, Joseph E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel recurrently mutated genes in African American colon cancers</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2015-01-27</date><risdate>2015</risdate><volume>112</volume><issue>4</issue><spage>1149</spage><epage>1154</epage><pages>1149-1154</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Significance Colorectal cancer is a leading cause of cancer-related deaths world-wide. African Americans exhibit the highest colon cancer incidence and mortality among all ethnic groups in the United States. Despite this finding, there is a dearth of knowledge on the genetic mechanisms underlying colon carcinogenesis in African Americans. We thus initiated this study to characterize the mutational landscapes of African American colon cancers. We identified new genes that are significantly mutated in colon cancer and that are highly preferentially targeted for mutations in colon cancers arising in African Americans as compared with Caucasians. These findings suggest differences in routes of colon carcinogenesis between the different ethnic groups and also may have implications for the ethnicity associated differences in tumor incidence and outcome.
We used whole-exome and targeted sequencing to characterize somatic mutations in 103 colorectal cancers (CRC) from African Americans, identifying 20 new genes as significantly mutated in CRC. Resequencing 129 Caucasian derived CRCs confirmed a 15-gene set as a preferential target for mutations in African American CRCs. Two predominant genes, ephrin type A receptor 6 ( EPHA6 ) and folliculin ( FLCN ), with mutations exclusive to African American CRCs, are by genetic and biological criteria highly likely African American CRC driver genes. These previously unsuspected differences in the mutational landscapes of CRCs arising among individuals of different ethnicities have potential to impact on broader disparities in cancer behaviors.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>25583493</pmid><doi>10.1073/pnas.1417064112</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | African Americans African Americans - genetics Biological Sciences carcinogenesis colon Colonic Neoplasms - ethnology Colonic Neoplasms - genetics Colorectal cancer colorectal neoplasms European Continental Ancestry Group - genetics Exome Female Genes Genetics Genome-Wide Association Study Health behavior Humans Male mortality Mutation Proto-Oncogene Proteins - genetics Receptor, EphA6 - genetics Tumor Suppressor Proteins - genetics United States Whites |
title | Novel recurrently mutated genes in African American colon cancers |
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