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中国宣威肺腺癌的全基因组测序分析。

Whole genome sequencing analysis of lung adenocarcinoma in Xuanwei, China.

机构信息

Department of Clinical Laboratory, First Affiliated Hospital of Kunming Medical University, Kunming, China.

Yunnan Institute of Diagnosis, Kunming, China.

出版信息

Thorac Cancer. 2017 Mar;8(2):88-96. doi: 10.1111/1759-7714.12411. Epub 2017 Jan 13.

Abstract

BACKGROUND

The lung cancer mortality rate in Xuanwei city is among the highest in China and adenocarcinoma is the major histological type. Lung cancer has been associated with exposure to indoor smoky coal emissions that contain high levels of polycyclic aromatic hydrocarbons; however, the pathogenesis of lung cancer has not yet been fully elucidated.

METHODS

We performed whole genome sequencing with lung adenocarcinoma and corresponding non-tumor tissue to explore the genomic features of Xuanwei lung cancer. We used the Molecule Annotation System to determine and plot alterations in genes and signaling pathways.

RESULTS

A total of 3 428 060 and 3 416 989 single nucleotide variants were detected in tumor and normal genomes, respectively. After comparison of these two genomes, 977 high-confidence somatic single nucleotide variants were identified. We observed a remarkably high proportion of C·G-A·T transversions. HECTD4, RCBTB2, KLF15, and CACNA1C may be cancer-related genes. Nine copy number variations increased in chromosome 5 and one in chromosome 7. The novel junctions were detected via clustered discordant paired ends and 1955 structural variants were discovered. Among these, we found 44 novel chromosome structural variations. In addition, EGFR and CACNA1C in the mitogen-activated protein kinase signaling pathway were mutated or amplified in lung adenocarcinoma tumor tissue.

CONCLUSION

We obtained a comprehensive view of somatic alterations of Xuanwei lung adenocarcinoma. These findings provide insight into the genomic landscape in order to further learn about the progress and development of Xuanwei lung adenocarcinoma.

摘要

背景

宣威市的肺癌死亡率位居中国之首,且主要组织学类型为腺癌。肺癌与接触含高水平多环芳烃的室内烟煤燃烧排放物有关;然而,肺癌的发病机制尚未完全阐明。

方法

我们对肺腺癌及相应的非肿瘤组织进行全基因组测序,以探索宣威肺癌的基因组特征。我们使用分子注释系统来确定和绘制基因和信号通路的改变。

结果

在肿瘤和正常基因组中分别检测到 3428060 和 3416989 个单核苷酸变异。对这两个基因组进行比较后,鉴定出 977 个高可信度的体细胞单核苷酸变异。我们观察到 C·G-A·T 颠换的比例非常高。HECTD4、RCBTB2、KLF15 和 CACNA1C 可能与癌症相关。染色体 5 上有 9 个拷贝数增加,染色体 7 上有 1 个。通过聚类不一致的配对末端检测到新的连接,发现 1955 个结构变异,其中包括 44 个新的染色体结构变异。此外,在肺腺癌肿瘤组织中,丝裂原激活蛋白激酶信号通路中的 EGFR 和 CACNA1C 发生了突变或扩增。

结论

我们获得了宣威肺腺癌体细胞改变的全面视图。这些发现为了解宣威肺腺癌的进展和发展提供了基因组景观的深入了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e96e/5334298/a0e9ed14eada/TCA-8-88-g001.jpg

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