Publication:
Signet ring cell colorectal cancer: genomic insights into a rare subpopulation of colorectal adenocarcinoma

dc.contributor.authorKrittiya Korphaisarnen_US
dc.contributor.authorVan Morrisen_US
dc.contributor.authorJenifer S. Davisen_US
dc.contributor.authorMichael J. Overmanen_US
dc.contributor.authorDavid R. Fogelmanen_US
dc.contributor.authorBryan K. Keeen_US
dc.contributor.authorArvind Dasarien_US
dc.contributor.authorKanwal P.S. Raghaven_US
dc.contributor.authorImad Shureiqien_US
dc.contributor.authorMetha Truptien_US
dc.contributor.authorRobert A. Wolffen_US
dc.contributor.authorCathy Engen_US
dc.contributor.authorDavid G. Menteren_US
dc.contributor.authorStanley Hamiltonen_US
dc.contributor.authorScott Kopetzen_US
dc.contributor.otherUniversity of Texas MD Anderson Cancer Centeren_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.date.accessioned2020-01-27T07:39:01Z
dc.date.available2020-01-27T07:39:01Z
dc.date.issued2019-09-10en_US
dc.description.abstract© 2019, The Author(s), under exclusive licence to Cancer Research UK. Background: Signet ring cell carcinoma (SRCC) is a rare subtype of colorectal cancer (CRC). The aim of this study was to characterise the genomic alterations and outcomes of SRCC. Methods: Medical records of metastatic CRC (mCRC) patients whose tumours were evaluated by NGS analysis were reviewed. SC-mCRC were classified into two groups: SRCC (>50% signet ring cells) and adenocarcinoma (AC) with SC component (≤50% signet ring cells). Results: Six hundred and sixty-five mCRC patients were included. Of the 93 mCRC cases with SC features, 63 had slides for review. Of those 63 cases, 35 were confirmed SRCC, and 28 were AC with SC component. Compared with AC group, KRAS and PIK3CA mutations (mts) were found in only 11% (OR: 0.13) and 3% (OR: 0.15) of SRCC cases, respectively. In contrast to the 44% rate of APC mts in AC group, only 3% of SRCC patients had APC mts (OR = 0.04). Conclusions: SRCC has distinct molecular features, including low rates of KRAS, PIK3CA and APC mts. Further study to identify activation pathways and potential therapeutic targets are needed.en_US
dc.identifier.citationBritish Journal of Cancer. Vol.121, No.6 (2019), 505-510en_US
dc.identifier.doi10.1038/s41416-019-0548-9en_US
dc.identifier.issn15321827en_US
dc.identifier.issn00070920en_US
dc.identifier.other2-s2.0-85070805278en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/50082
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85070805278&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleSignet ring cell colorectal cancer: genomic insights into a rare subpopulation of colorectal adenocarcinomaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85070805278&origin=inwarden_US

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