Frequent alterations in cytoskeleton remodelling genes in primary and metastatic lung adenocarcinomas
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Frequent alterations in cytoskeleton remodelling genes in primary and metastatic lung adenocarcinomas. / Wu, Kui; Zhang, Xin; Li, Fuqiang; Xiao, Dakai; Hou, Yong; Zhu, Shida; Liu, Dongbing; Ye, Xiaofei; Ye, Mingzhi; Yang, Jie; Shao, Libin; Pan, Hui; Lu, Na; Yu, Yuan; Liu, Liping; Li, Jin; Huang, Liyan; Tang, Hailing; Deng, Qiuhua; Zheng, Yue; Peng, Lihua; Liu, Geng; Gu, Xia; He, Ping; Gu, Yingying; Lin, Weixuan; He, Huiming; Xie, Guoyun; Liang, Han; An, Na; Wang, Hui; Teixeira, Manuel; Vieira, Joana; Liang, Wenhua; Zhao, Xin; Peng, Zhiyu; Mu, Feng; Zhang, Xiuqing; Xu, Xun; Yang, Huanming; Kristiansen, Karsten; Zhong, Nanshan; Wang, Jun; Pan-Hammarström, Qiang; He, Jianxing; Wang, Jian.
In: Nature Communications, Vol. 6, 10131, 2015.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Frequent alterations in cytoskeleton remodelling genes in primary and metastatic lung adenocarcinomas
AU - Wu, Kui
AU - Zhang, Xin
AU - Li, Fuqiang
AU - Xiao, Dakai
AU - Hou, Yong
AU - Zhu, Shida
AU - Liu, Dongbing
AU - Ye, Xiaofei
AU - Ye, Mingzhi
AU - Yang, Jie
AU - Shao, Libin
AU - Pan, Hui
AU - Lu, Na
AU - Yu, Yuan
AU - Liu, Liping
AU - Li, Jin
AU - Huang, Liyan
AU - Tang, Hailing
AU - Deng, Qiuhua
AU - Zheng, Yue
AU - Peng, Lihua
AU - Liu, Geng
AU - Gu, Xia
AU - He, Ping
AU - Gu, Yingying
AU - Lin, Weixuan
AU - He, Huiming
AU - Xie, Guoyun
AU - Liang, Han
AU - An, Na
AU - Wang, Hui
AU - Teixeira, Manuel
AU - Vieira, Joana
AU - Liang, Wenhua
AU - Zhao, Xin
AU - Peng, Zhiyu
AU - Mu, Feng
AU - Zhang, Xiuqing
AU - Xu, Xun
AU - Yang, Huanming
AU - Kristiansen, Karsten
AU - Zhong, Nanshan
AU - Wang, Jun
AU - Pan-Hammarström, Qiang
AU - He, Jianxing
AU - Wang, Jian
PY - 2015
Y1 - 2015
N2 - 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.
AB - 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.
U2 - 10.1038/ncomms10131
DO - 10.1038/ncomms10131
M3 - Journal article
C2 - 26647728
AN - SCOPUS:84949570896
VL - 6
JO - Nature Communications
JF - Nature Communications
SN - 2041-1723
M1 - 10131
ER -
ID: 153601752