PT - JOURNAL ARTICLE AU - SAURABH YADAV AU - NAVONIL DE SARKAR AU - NIRAJ KUMARI AU - NARENDRA KRISHNANI AU - ASHOK KUMAR AU - BALRAJ MITTAL TI - Targeted Gene Sequencing of Gallbladder Carcinoma Identifies High-impact Somatic and Rare Germline Mutations DP - 2017 Nov 01 TA - Cancer Genomics - Proteomics PG - 495--506 VI - 14 IP - 6 4099 - http://cgp.iiarjournals.org/content/14/6/495.short 4100 - http://cgp.iiarjournals.org/content/14/6/495.full SO - Cancer Genomics Proteomics2017 Nov 01; 14 AB - Background: Gallbladder carcinoma (GBC) is a subtype of biliary tract malignancy with poor prognosis and high fatality rate. The present study was designed to uncover somatic and rare germline mutations in GBC to reveal the disease biology and understand the clinical importance of mutation profile in terms of prognostics and actionability. Materials and Methods: We performed ultra-deep sequencing across 409 cancer-related genes in 11 GBC patients of North-Indian descent. NGS data analysis was performed using Ion Reporter and several other publicly available resources and databases. Results: We identified 184 nonsynonymous somatic and 60 rare germline mutations in bona-fide cancer drivers such as SMAD family member 4 (SMAD4), lysine methyltransferase 2C (KMT2C), and tumor protein p53 (TP53). All the early-onset cases or hypermutated cases harbored mutation(s) in critical DNA-repair genes. Additionally, we detected 9 novel genes with high-impact somatic mutations in GBC. Conclusion: Our results indicated the significance of inherited rare germline mutations in DNA-repair pathway genes in addition to acquired somatic mutations in GB carcinogenesis.