| Literature DB >> 28040546 |
Maolan Li1, Fatao Liu1, Yijian Zhang1, Xiangsong Wu1, Wenguang Wu1, Xu-An Wang1, Shuai Zhao1, Shibo Liu1, Haibin Liang1, Fei Zhang1, Qiang Ma1, Shanshan Xiang1, Huaifeng Li1, Lin Jiang1, Yunping Hu1, Wei Gong1, Yun Zhang2, Tieliang Ma2, Kai Zhang3, Yun Liu4, Yingbin Liu5.
Abstract
Small-cell gallbladder neuroendocrine carcinoma (GB-SCNEC) is a relatively rare histological type of gallbladder cancer, and the genomic landscape of GB-SCNEC is rarely considered in treatment decisions. We performed whole-genome sequencing on an advanced case of GB-SCNEC. We identified approximately 900 high-quality somatic single nucleotide variants (SNVs) and small insertions and deletions (INDELs), 109 of which were shared by both the primary and metastatic tumor tissues. Somatic non-synonymous coding variations with damaging impact in HMCN1 and CDH10 were observed in both the primary and metastatic tissue specimens. A pathway analysis of the genes mapped to the SNVs and INDELs revealed gene enrichment associated with axon guidance, ERBB signaling et al. Furthermore, we identified 11 deletions, 4 tandem duplications and 5 inversions that mapped to known genes. Two gene fusions, NCAM2-SGCZ and BTG3-CCDC40 were also discovered and validated by Sanger sequencing. Additionally, we identified genome-wide copy number variations and microsatellite instability. In this study, we identified novel biological markers of GB-SCNEC that may serve as valuable prognostic factors or indicators of treatment response in patients with GB-SCNEC with lymphatic metastasis.Entities:
Keywords: Gallbladder cancer; Small-cell gallbladder neuroendocrine carcinoma; Variation; Whole-genome sequencing
Mesh:
Year: 2016 PMID: 28040546 DOI: 10.1016/j.canlet.2016.12.027
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679