作者
Jianbin Chen,Hechuan Yang,Audrey Su Min Teo,Lubna Amer,Faranak Ghazi Sherbaf,Chu Quan Tan,Jacob J.S. Alvarez,Bingxin Lu,Jia Qi Lim,Angela Takano,Rahul Nahar,Yin Yeng Lee,Clifton Phua,Khi Pin Chua,Lisda Suteja,Pauline Jieqi Chen,Mei Mei Chang,Tina Koh,Boon‐Hean Ong,Devanand Anantham,Anne Ann Ling Hsu,Apoorva Gogna,Chow Wei Too,Zaw Win Aung,Yi Fei Lee,Lanying Wang,Kiat Hon Lim,Andreas Wilm,Poh Sum D. Choi,Poh Yong Ng,Chee‐Keong Toh,Wan‐Teck Lim,Siming Ma,Bing Lim,Jin Liu,Wai Leong Tam,Anders J. Skanderup,Joe Yeong,Eng-Huat Tan,Caretha L. Creasy,Daniel S.W. Tan,Axel M. Hillmer,Weiwei Zhai
摘要
Lung cancer is the world’s leading cause of cancer death and shows strong ancestry disparities. By sequencing and assembling a large genomic and transcriptomic dataset of lung adenocarcinoma (LUAD) in individuals of East Asian ancestry (EAS; n = 305), we found that East Asian LUADs had more stable genomes characterized by fewer mutations and fewer copy number alterations than LUADs from individuals of European ancestry. This difference is much stronger in smokers as compared to nonsmokers. Transcriptomic clustering identified a new EAS-specific LUAD subgroup with a less complex genomic profile and upregulated immune-related genes, allowing the possibility of immunotherapy-based approaches. Integrative analysis across clinical and molecular features showed the importance of molecular phenotypes in patient prognostic stratification. EAS LUADs had better prediction accuracy than those of European ancestry, potentially due to their less complex genomic architecture. This study elucidated a comprehensive genomic landscape of EAS LUADs and highlighted important ancestry differences between the two cohorts. Genomic and transcriptomic analysis of lung adenocarcinoma (LUAD) in Asia indicates that Asian LUADs have fewer mutations, lower driver prevalence and fewer copy number alterations than European LUADs.