Characterization of the genomic landscape in large- scale Chinese patients with pancreatic cancer

被引:45
作者
Zhang, Xiaofei [1 ]
Mao, Tiebo [1 ]
Zhang, Bei [2 ]
Xu, Haiyan [1 ]
Cui, Jiujie [1 ]
Jiao, Feng [1 ]
Chen, Dongqin [1 ]
Wang, Yu [1 ]
Hu, Jiong [1 ]
Xia, Qing [1 ]
Ge, Weiyu [1 ]
Li, Shumin [1 ]
Yue, Ming [1 ]
Ma, Jingyu [1 ]
Yao, Jiayu [1 ]
Wang, Yongchao [1 ]
Wang, Yanling [1 ]
Shentu, Daiyuan [1 ]
Zhang, Xiao [1 ]
Chen, Shiqing [2 ]
Bai, Yuezong [2 ]
Wang, Yuexiang [7 ]
Zhang, Xuebin [6 ]
Liu, Qiang [5 ]
Sun, Yongwei [3 ]
Fu, Deliang [4 ]
Liu, Yingbin [3 ]
Xiong, Lei [2 ]
Wang, Liwei [1 ]
机构
[1] Shanghai Jiao Tong Univ, State Key Lab Oncogenes & Related Genes, Shanghai Canc Inst, Dept Oncol,Renji Hosp,Sch Med, 160 Pujian Rd, Shanghai 200127, Peoples R China
[2] 3D Med Inc, Med Dept, Shanghai 201321, Peoples R China
[3] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Dept Biliary Pancreat Surg, Shanghai, Peoples R China
[4] Fudan Univ, Shanghai Med Coll, Huashan Hosp, Dept Pancreat Surg,Pancreat Dis Inst, Shanghai, Peoples R China
[5] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Dept Pathol, Shanghai, Peoples R China
[6] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Dept Intervent Oncol, Shanghai, Peoples R China
[7] Chinese Acad Sci, Shanghai Inst Nutr & Hlth, Lab Canc Progress & Translat Med, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Pancreatic ductal adenocarcinoma; genomic mutation; next -generation sequencing; KRAS; DNA damage; response; DNA-DAMAGE; GEMCITABINE; STATISTICS; GENES;
D O I
10.1016/j.ebiom.2022.103897
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Pancreatic ductal adenocarcinoma (PDAC) is a malignant tumor with an extremely poor prognosis. Effective targets for anticancer therapy confirmed in PDAC are limited. However, the characteristics of genomics have not been fully elucidated in large-scale patients with PDAC from China.& nbsp;Methods We collected both blood and tissue samples from 1080 Chinese patients with pancreatic cancer and retro-spectively investigated the genomic landscape using next-generation sequencing (NGS).& nbsp;Findings We found recurrent somatic mutations in KRAS (83.2%), TP53 (70.6%), CDKN2A (28.8%), SMAD4 (23.0%), ARID1A (12.8%) and CDKN2B (8.9%) in Chinese PDAC patients. Compared with primary pancreatic can-cers, more genomic alterations accumulated especially cell cycle regulatory gene variants (45.4% vs 31.6%, P < 0.001) were observed in metastatic tumors. The most common mutation site of KRAS is p.G12D (43.6%) in pancre-atic cancer. Patients with KRAS mutations were significantly associated with older age and mutations in the other three driver genes, while KRAS wild-type patients contained more fusion mutations and alternative mechanisms of RTK/Ras/MAPK pathway including a number of clinically targetable mutations. KRAS mutations in Chinese cohort were significantly lower than those in Western cohorts (all P < 0.05). A total of 252 (23.3%) patients with the core DNA damage response (DDR) gene mutations were detected. ATM (n =59, 5.5%) was the most frequent mutant DDR gene in patients with pancreatic cancer from China. Patients with germline DDR gene mutations were younger (P = 0.018), while patients with somatic DDR gene mutations were more likely to accumulate in metastatic lesions (P < 0.001) and had higher TMB levels (P < 0.001). In addition, patients with mutant DDR genes and patients carrying TP53 mutation were observed mutually exclusive (P < 0.001).& nbsp;Interpretation We demonstrated the real-world genomic characteristics of large-scale patients with pancreatic can-cer from China which may have promising implications for further clinical significance and drug development.& nbsp;Funding The funders are listed in the Acknowledgement. Copyright (C)& nbsp;2022 The Authors. Published by Elsevier B.V.& nbsp;
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页数:13
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