前列腺癌
色丛
癌症
前列腺
TMPRS2型
外显子组
PTEN公司
医学
体细胞
外显子组测序
生殖系
疾病
种系突变
遗传学
肿瘤科
生物
突变
基因
内科学
PCA3系列
细胞凋亡
传染病(医学专业)
PI3K/AKT/mTOR通路
2019年冠状病毒病(COVID-19)
作者
Karla Lindquist,Pamela L. Paris,Thomas J. Hoffmann,Niall J. Cardin,Rémi Kazma,Joel Mefford,Jeffrey P. Simko,Vy Ngo,Yalei Chen,Albert M. Levin,Dhananjay Chitale,Brian T. Helfand,William J. Catàlona,Benjamin A. Rybicki,John S. Witte
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2016-02-27
卷期号:76 (7): 1860-1868
被引量:71
标识
DOI:10.1158/0008-5472.can-15-1787
摘要
Prostate cancer is the most frequently diagnosed and second most fatal nonskin cancer among men in the United States. African American men are two times more likely to develop and die of prostate cancer compared with men of other ancestries. Previous whole genome or exome tumor-sequencing studies of prostate cancer have primarily focused on men of European ancestry. In this study, we sequenced and characterized somatic mutations in aggressive (Gleason ≥7, stage ≥T2b) prostate tumors from 24 African American patients. We describe the locations and prevalence of small somatic mutations (up to 50 bases in length), copy number aberrations, and structural rearrangements in the tumor genomes compared with patient-matched normal genomes. We observed several mutation patterns consistent with previous studies, such as large copy number aberrations in chromosome 8 and complex rearrangement chains. However, TMPRSS2-ERG gene fusions and PTEN losses occurred in only 21% and 8% of the African American patients, respectively, far less common than in patients of European ancestry. We also identified mutations that appeared specific to or more common in African American patients, including a novel CDC27-OAT gene fusion occurring in 17% of patients. The genomic aberrations reported in this study warrant further investigation of their biologic significant role in the incidence and clinical outcomes of prostate cancer in African Americans. Cancer Res; 76(7); 1860-8. ©2016 AACR.
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