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Frequent alterations in cytoskeleton remodelling genes in primary and metastatic lung adenocarcinomas

  • Kui Wu
  • , Xin Zhang
  • , Fuqiang Li
  • , Dakai Xiao
  • , Yong Hou
  • , Shida Zhu
  • , Dongbing Liu
  • , Xiaofei Ye
  • , Mingzhi Ye
  • , Jie Yang
  • , Libin Shao
  • , Hui Pan
  • , Na Lu
  • , Yuan Yu
  • , Liping Liu
  • , Jin Li
  • , Liyan Huang
  • , Hailing Tang
  • , Qiuhua Deng
  • , Yue Zheng
  • Lihua Peng, Geng Liu, Xia Gu, Ping He, Yingying Gu, Weixuan Lin, Huiming He, Guoyun Xie, Han Liang, Na An, Hui Wang, Manuel Teixeira, Joana Vieira, Wenhua Liang, Xin Zhao, Zhiyu Peng, Feng Mu, Xiuqing Zhang, Xun Xu, Huanming Yang, Karsten Kristiansen, Nanshan Zhong, Jun Wang, Qiang Pan-Hammarström, Jianxing He, Jian Wang
  • BGI-Shenzhen
  • The First Affiliated Hospital of Guanzhou Medical University
  • Guangzhou Medical College
  • National Clinical Research Center for Respiratory Disease
  • University of Copenhagen
  • Karolinska Institutet
  • Guangzhou Key Laboratory of Cancer Trans-Omics Research
  • Instituto Português de Oncologia do Porto Francisco Gentil E.P.E.
  • Zhejiang University

科研成果: 期刊稿件 › 文章 › 同行评审

94 引用 (Scopus)

摘要

The landscape of genetic alterations in lung adenocarcinoma derived from Asian patients is largely uncharacterized. Here we present an integrated genomic and transcriptomic analysis of 335 primary lung adenocarcinomas and 35 corresponding lymph node metastases from Chinese patients. Altogether 13 significantly mutated genes are identified, including the most commonly mutated gene TP53 and novel mutation targets such as RHPN2, GLI3 and MRC2. TP53 mutations are furthermore significantly enriched in tumours from patients harbouring metastases. Genes regulating cytoskeleton remodelling processes are also frequently altered, especially in metastatic samples, of which the high expression level of IQGAP3 is identified as a marker for poor prognosis. Our study represents the first large-scale sequencing effort on lung adenocarcinoma in Asian patients and provides a comprehensive mutational landscape for both primary and metastatic tumours. This may thus form a basis for personalized medical care and shed light on the molecular pathogenesis of metastatic lung adenocarcinoma.

源语言英语
期刊论文编号10131
期刊Nature Communications
卷6
DOI
出版状态已出版 - 9 12月 2015
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