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Whole-Exome Sequencing of Tumor-only Samples Reveals the Association between Somatic Alterations and Clinical Features in Pancreatic Cancer

Author(s):

Wenwen Ran, Xiangbin Chen , Bo Wang, Ping Yang, Yongxing Li, Yujing Xiao, Xiaonan Wang, Guangqi Li, Lili Wang, Yingmin Han, Yonggang Peng, Jidong Lang, Yuebin Liang, Yupei Xiao, Qingqing Lu*, Huixin Lin , Geng Tian, Dawei Yuan, Chaoyang Deng, Jialiang Yang and Xiaoming Xing   Pages 1 - 8 ( 8 )

Abstract:


Background: Identification of genomic markers using NGS (next generation sequencing) technology would be valuable for guiding precision medicine treatments for pancreatic cancers. Traditional somatic mutation methods require both tumor and matched non-tumor samples. However, only tumor samples are available in most times, especially in retrospective studies. In this study, we tried to analyze the associations between clinical features and oncogenic somatic mutations in genome-wide from tumor-only samples.

Method: 54 tumor-only samples derived from pancreatic cancer patients were used for whole-exome sequencing. An approach involving SNP filtering of variants included in Catalogue of Somatic Mutations in Cancer (COSMIC) database was used to identify oncogenic somatic mutations. The relationships between oncogenic mutations and clinical features were analyzed and simultaneously compared with those from the TCGA database.

Results: By analyzing the mutations from tumor only samples, divergent mutation profiles were observed in different locations (head vs body/tail) of pancreatic tumors. The divergences between pancreatic head and body/tail cancers were also confirmed by the TCGA data. Furthermore, mutations of several genes were found significantly associated with clinical features, such as pathological stage and the degree of tumor differentiation.

Conclusion: The results confirmed the efficiency of our approach for identifying oncogenic somatic mutations from tumor only samples and revealed the associations between somatic mutations and clinical features in pancreatic cancer.

Keywords:

oncogenic somatic mutation, clinical pathogenic factors, association, pancreatic cancer, NGS

Affiliation:

Department of Pathology, The Affiliated Hospital of Qingdao University, Qingdao 266003, Geneis Beijing Co., Ltd., Beijing 100102, Geneis Beijing Co., Ltd., Beijing 100102, Department of Pathology, Yantai Yuhuangding Hospital, Yantai 264000, Department of Pathology, The Affiliated Hospital of Qingdao University, Qingdao 266003, Department of Pathology, The Affiliated Hospital of Qingdao University, Qingdao 266003, Department of Pathology, The Affiliated Hospital of Qingdao University, Qingdao 266003, Department of Pathology, The Affiliated Hospital of Qingdao University, Qingdao 266003, Department of Pathology, The Affiliated Hospital of Qingdao University, Qingdao 266003, Geneis Beijing Co., Ltd., Beijing 100102, Geneis Beijing Co., Ltd., Beijing 100102, Geneis Beijing Co., Ltd., Beijing 100102, Geneis Beijing Co., Ltd., Beijing 100102, Geneis Beijing Co., Ltd., Beijing 100102, Geneis Beijing Co., Ltd., Beijing 100102, Geneis Beijing Co., Ltd., Beijing 100102, Geneis Beijing Co., Ltd., Beijing 100102, Geneis Beijing Co., Ltd., Beijing 100102, Geneis Beijing Co., Ltd., Beijing 100102, Geneis Beijing Co., Ltd., Beijing 100102, Department of Pathology, The Affiliated Hospital of Qingdao University, Qingdao 266003



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