Comparative Molecular Analysis of Gastrointestinal Adenocarcinomas.

Liu Y, Sethi NS, Hinoue T, Schneider BG, Cherniack AD, Sanchez-Vega F, Seoane JA, Farshidfar F, Bowlby R, Islam M, Kim J, Chatila W, Akbani R, Kanchi RS, Rabkin CS, Willis JE, Wang KK, Mccall SJ, Mishra L, Ojesina AI, Bullman S, Pedamallu CS, Lazar AJ, Sakai R, Thorsson V, Bass AJ, Laird PW (2018)


Publication Type: Journal article

Publication year: 2018

Journal

Book Volume: 33

Pages Range: 721-735.e8

Journal Issue: 4

DOI: 10.1016/j.ccell.2018.03.010

Abstract

We analyzed 921 adenocarcinomas of the esophagus, stomach, colon, and rectum to examine shared and distinguishing molecular characteristics of gastrointestinal tract adenocarcinomas (GIACs). Hypermutated tumors were distinct regardless of cancer type and comprised those enriched for insertions/deletions, representing microsatellite instability cases with epigenetic silencing of MLH1 in the context of CpG island methylator phenotype, plus tumors with elevated single-nucleotide variants associated with mutations in POLE. Tumors with chromosomal instability were diverse, with gastroesophageal adenocarcinomas harboring fragmented genomes associated with genomic doubling and distinct mutational signatures. We identified a group of tumors in the colon and rectum lacking hypermutation and aneuploidy termed genome stable and enriched in DNA hypermethylation and mutations in KRAS, SOX9, and PCBP1.

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How to cite

APA:

Liu, Y., Sethi, N.S., Hinoue, T., Schneider, B.G., Cherniack, A.D., Sanchez-Vega, F.,... Laird, P.W. (2018). Comparative Molecular Analysis of Gastrointestinal Adenocarcinomas. Cancer Cell, 33(4), 721-735.e8. https://doi.org/10.1016/j.ccell.2018.03.010

MLA:

Liu, Yang, et al. "Comparative Molecular Analysis of Gastrointestinal Adenocarcinomas." Cancer Cell 33.4 (2018): 721-735.e8.

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