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Whole-genome and Transcriptome Sequencing of Prostate Cancer Identify New Genetic Alterations Driving Disease Progression

前列腺癌 医学 转录组 疾病 基因组 全基因组测序 DNA测序 基因 生物 癌症 计算生物学 生物信息学 遗传学 内科学 基因表达
作者
Shancheng Ren,Gong‐Hong Wei,Dongbing Liu,Liguo Wang,Yong Hou,Shida Zhu,Lihua Peng,Qin Zhang,Yanbing Cheng,Hong Su,Xiuqing Zhou,Jibin Zhang,Fuqiang Li,Hancheng Zheng,Zhikun Zhao,Changjun Yin,Zengquan He,Xīn Gào,Haiyen E. Zhau,Chia-Yi Chu
出处
期刊:European Urology [Elsevier BV]
卷期号:73 (3): 322-339 被引量:187
标识
DOI:10.1016/j.eururo.2017.08.027
摘要

Global disparities in prostate cancer (PCa) incidence highlight the urgent need to identify genomic abnormalities in prostate tumors in different ethnic populations including Asian men.To systematically explore the genomic complexity and define disease-driven genetic alterations in PCa.The study sequenced whole-genome and transcriptome of tumor-benign paired tissues from 65 treatment-naive Chinese PCa patients. Subsequent targeted deep sequencing of 293 PCa-relevant genes was performed in another cohort of 145 prostate tumors.The genomic alteration landscape in PCa was analyzed using an integrated computational pipeline. Relationships with PCa progression and survival were analyzed using nonparametric test, log-rank, and multivariable Cox regression analyses.We demonstrated an association of high frequency of CHD1 deletion with a low rate of TMPRSS2-ERG fusion and relatively high percentage of mutations in androgen receptor upstream activator genes in Chinese patients. We identified five putative clustered deleted tumor suppressor genes and provided experimental and clinical evidence that PCDH9, deleted/loss in approximately 23% of tumors, functions as a novel tumor suppressor gene with prognostic potential in PCa. Furthermore, axon guidance pathway genes were frequently deregulated, including gain/amplification of PLXNA1 gene in approximately 17% of tumors. Functional and clinical data analyses showed that increased expression of PLXNA1 promoted prostate tumor growth and independently predicted prostate tumor biochemical recurrence, metastasis, and poor survival in multi-institutional cohorts of patients with PCa. A limitation of this study is that other genetic alterations were not experimentally investigated.There are shared and salient genetic characteristics of PCa in Chinese and Caucasian men. Novel genetic alterations in PCDH9 and PLXNA1 were associated with disease progression.We reported the first large-scale and comprehensive genomic data of prostate cancer from Asian population. Identification of these genetic alterations may help advance prostate cancer diagnosis, prognosis, and treatment.
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