Author
Listed:
- Shaodong Hong
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Dongbing Liu
(BGI-Shenzhen
China National GeneBank-Shenzhen, BGI-Shenzhen)
- Shuzhen Luo
(BGI-Shenzhen
China National GeneBank-Shenzhen, BGI-Shenzhen)
- Wenfeng Fang
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Jianhua Zhan
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Sha Fu
(Sun Yat-Sen University
Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation)
- Yaxiong Zhang
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Xuan Wu
(Sun Yat-sen University Cancer Center
Peking University Shenzhen Hospital)
- Huaqiang Zhou
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Xi Chen
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Gang Chen
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Zhonghan Zhang
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Qiufan Zheng
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Xiaobo Li
(BGI-Shenzhen
China National GeneBank-Shenzhen, BGI-Shenzhen
University of Chinese Academy of Sciences)
- Jinghao Chen
(BGI-Shenzhen
China National GeneBank-Shenzhen, BGI-Shenzhen
University of Chinese Academy of Sciences)
- Xingmin Liu
(BGI-Shenzhen)
- Mengyue Lei
(BGI-Shenzhen
China National GeneBank-Shenzhen, BGI-Shenzhen)
- Chen Ye
(BGI-Shenzhen
China National GeneBank-Shenzhen, BGI-Shenzhen)
- Jian Wang
(BGI-Shenzhen
China National GeneBank-Shenzhen, BGI-Shenzhen)
- Huanming Yang
(BGI-Shenzhen
China National GeneBank-Shenzhen, BGI-Shenzhen)
- Xun Xu
(BGI-Shenzhen
China National GeneBank-Shenzhen, BGI-Shenzhen)
- Shida Zhu
(BGI-Shenzhen
China National GeneBank-Shenzhen, BGI-Shenzhen)
- Yunpeng Yang
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Yuanyuan Zhao
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Ningning Zhou
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Hongyun Zhao
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Yan Huang
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
- Lanjun Zhang
(State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine
Sun Yat-sen University Cancer Center)
- Kui Wu
(BGI-Shenzhen
China National GeneBank-Shenzhen, BGI-Shenzhen)
- Li Zhang
(Sun Yat-sen University Cancer Center
State Key Laboratory of Oncology in South China
Collaborative Innovation Center for Cancer Medicine)
Abstract
Pulmonary lymphoepithelioma-like carcinoma (LELC) is a rare and distinct subtype of primary lung cancer characterized by Epstein-Barr virus (EBV) infection. Herein, we reported the mutational landscape of pulmonary LELC using whole-exome sequencing, targeted deep sequencing and single-nucleotide polymorphism arrays. We identify a low degree of somatic mutation but widespread existence of copy number variations. We reveal predominant signature 2 mutations and frequent loss of type I interferon genes that are involved in the host-virus counteraction. Integrated analysis shows enrichment of genetic lesions affecting several critical pathways, including NF-κB, JAK/STAT, and cell cycle. Notably, multi-dimensional comparison unveils that pulmonary LELC resemble NPC but are clearly different from other lung cancers, natural killer/T-cell lymphoma or EBV-related gastric cancer in terms of genetic features. In all, our study illustrates a distinct genomic landscape of pulmonary LELC and provides a road map to facilitate genome-guided personalized treatment.
Suggested Citation
Shaodong Hong & Dongbing Liu & Shuzhen Luo & Wenfeng Fang & Jianhua Zhan & Sha Fu & Yaxiong Zhang & Xuan Wu & Huaqiang Zhou & Xi Chen & Gang Chen & Zhonghan Zhang & Qiufan Zheng & Xiaobo Li & Jinghao , 2019.
"The genomic landscape of Epstein-Barr virus-associated pulmonary lymphoepithelioma-like carcinoma,"
Nature Communications, Nature, vol. 10(1), pages 1-12, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-10902-w
DOI: 10.1038/s41467-019-10902-w
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