Hispanic/Latino Patients with Gastric Adenocarcinoma Have Distinct Molecular Profiles Including a High Rate of Germline CDH1 Variants

被引:22
作者
Wang, Sam C. [1 ]
Yeu, Yunku [2 ]
Hammer, Suntrea T. G. [3 ]
Xiao, Shu [1 ]
Zhu, Min [4 ,5 ]
Hong, Changjin [2 ]
Clemenceau, Jean R. [2 ]
Yoon, Lynn Y. [1 ]
Nassour, Ibrahim [1 ]
Shen, Jeanne [6 ]
Agarwal, Deepak [7 ]
Reznik, Scott I. [8 ]
Mansour, John C. [1 ]
Yopp, Adam C. [1 ]
Zhu, Hao [4 ,5 ]
Hwang, Tae Hyun [2 ]
Porembka, Matthew R. [1 ]
机构
[1] Univ Texas Southwestern Med Ctr, Dept Surg, Dallas, TX USA
[2] Cleveland Clin, Lerner Res Inst, Dept Quantitat Hlth Sci, Cleveland, OH 44106 USA
[3] Univ Texas Southwestern Med Ctr, Dept Pathol, Dallas, TX USA
[4] Univ Texas Southwestern Med Ctr, Childrens Res Inst, Ctr Regenerat Sci & Med, Dept Pediat, Dallas, TX USA
[5] Univ Texas Southwestern Med Ctr, Childrens Res Inst, Ctr Regenerat Sci & Med, Dept Internal Med, Dallas, TX USA
[6] Stanford Univ, Dept Pathol, Sch Med, Stanford, CA 94305 USA
[7] Univ Texas Austin, Dept Internal Med, Austin, TX 78712 USA
[8] Univ Texas Southwestern Med Ctr, Dept Cardiovasc & Thorac Surg, Dallas, TX USA
关键词
GENETIC ANCESTRY; BREAST-CANCER; MUTATIONS; DISPARITIES; AMPLIFICATION; DIVERSITY; SURVIVAL; SUBTYPES; RISK; MYC;
D O I
10.1158/0008-5472.CAN-19-2918
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hispanic/Latino patients have a higher incidence of gastric cancer and worse cancer-related outcomes compared with patients of other backgrounds. Whether there is a molecular basis for these disparities is unknown, as very few Hispanic/Latino patients have been included in previous studies. To determine the genomic landscape of gastric cancer in Hispanic/Latino patients, we performed whole-exome sequencing (WES) and RNA sequencing on tumor samples from 57 patients; germline analysis was conducted on 83 patients. The results were compared with data from Asian and White patients published by The Cancer Genome Atlas. Hispanic/Latino patients had a significantly larger proportion of genomically stable subtype tumors compared with Asian and White patients (65% vs. 21% vs. 20%, P < 0.001). Transcriptomic analysis identified molecular signatures that were prognostic. Of the 43 Hispanic/Latino patients with diffuse-type cancer, 7 (16%) had germline variants in CDH1. Variant carriers were significantly younger than noncarriers (41 vs. 50 years, P < 0.05). In silico algorithms predicted five variants to be deleterious. For two variants that were predicted to be benign, in vitro modeling demonstrated that these mutations conferred increased migratory capability, suggesting pathogenicity. Hispanic/Latino patients with gastric cancer possess unique genomic landscapes, including a high rate of CDH1 germline variants that may partially explain their aggressive clinical phenotypes. Individualized screening, genetic counseling, and treatment protocols based on patient ethnicity and race may be necessary. Significance: Gastric cancer in Hispanic/Latino patients has unique genomic profiles that may contribute to the aggressive clinical phenotypes seen in these patients.
引用
收藏
页码:2114 / 2124
页数:11
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