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Comprehensive molecular characterization of gastric adenocarcinoma

Adam J. Bass, Natalie Tasman, Brady Bernard, Roger Kramer, Michael Miller, Vésteinn Thórsson, Ilya Shmulevich, Lisa Iype, Hector Rovira, Richard Kreisberg, Sheila M. Reynolds, Timothy J. Triche, Moiz S. Bootwalla, Phillip H. Lai, Hui Shen

Nature · 2014 · ▲ 6,485 citations

Abstract

Gastric cancer is a leading cause of cancer deaths, but analysis of its molecular and clinical characteristics has been complicated by histological and aetiological heterogeneity. Here we describe a comprehensive molecular evaluation of 295 primary gastric adenocarcinomas as part of The Cancer Genome Atlas (TCGA) project. We propose a molecular classification dividing gastric cancer into four subtypes: tumours positive for Epstein–Barr virus, which display recurrent PIK3CA mutations, extreme DNA hypermethylation, and amplification of JAK2, CD274 (also known as PD-L1) and PDCD1LG2 (also known as PD-L2); microsatellite unstable tumours, which show elevated mutation rates, including mutations of genes encoding targetable oncogenic signalling proteins; genomically stable tumours, which are enriched for the diffuse histological variant and mutations of RHOA or fusions involving RHO-family GTPase-activating proteins; and tumours with chromosomal instability, which show marked aneuploidy and focal amplification of receptor tyrosine kinases. Identification of these subtypes provides a roadmap for patient stratification and trials of targeted therapies. The Cancer Genome Atlas reports on molecular evaluation of 295 primary gastric adenocarcinomas and proposes a new classification of gastric cancers into 4 subtypes, which should help with clinical assessment and trials of targeted therapies. This contribution from The Cancer Genome Atlas (TCGA) project describes the molecular evaluation of 295 primary gastric adenocarcinomas. Based on the results, the authors propose a novel classification separating gastric cancers into four subtypes according to: Epstein–Barr virus positive status, microsatellite instability, chromosomal instability or genomic stability. Given the histologic and etiologic heterogeneity of gastric cancer identification of these subtypes, using a schema that can readily be applied to patient samples should help with patient stratification and trials of targeted therapies.

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OpenAlex
DOI
10.1038/nature13480
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2026-06-04 MST

Cite this

APA
Bass, A.J., Tasman, N., Bernard, B., Kramer, R., Miller, M., Thórsson, V., Shmulevich, I., Iype, L., Rovira, H., Kreisberg, R., Reynolds, S.M., Triche, T.J., Bootwalla, M.S., Lai, P.H., Shen, H., Hinoue, T., Weisenberger, D.J., Berg, D.V.D., Laird, P.W., &amp; Curtis, C. (2014). Comprehensive molecular characterization of gastric adenocarcinoma. <em>Nature</em>. https://doi.org/10.1038/nature13480
Vancouver
Bass AJ, Tasman N, Bernard B, Kramer R, Miller M, Thórsson V, et al. Comprehensive molecular characterization of gastric adenocarcinoma. Nature. 2014. doi:10.1038/nature13480.
BibTeX
@article{adam2014Compre, title = {Comprehensive molecular characterization of gastric adenocarcinoma}, author = {Adam J. Bass and Natalie Tasman and Brady Bernard and Roger Kramer and Michael Miller and Vésteinn Thórsson and Ilya Shmulevich and Lisa Iype and Hector Rovira and Richard Kreisberg and Sheila M. Reynolds and Timothy J. Triche and Moiz S. Bootwalla and Phillip H. Lai and Hui Shen and Toshinori Hinoue and Daniel J. Weisenberger and David Van Den Berg and Peter W. Laird and Christina Curtis and Nikolaus Schultz and Jianjiong Gao and Nils Weinhold}, journal = {Nature}, year = {2014}, doi = {10.1038/nature13480}, }

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