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多个肺结节的突变模式与早期肺腺癌相关。

Mutational Pattern in Multiple Pulmonary Nodules Are Associated With Early Stage Lung Adenocarcinoma.

作者信息

Dong Shao-Wei, Li Rong, Cheng Zhiqiang, Liu Dong-Cheng, Xia Jinquan, Xu Jing, Li Shixuan, Wang Jian, Yue Yongjian, Fan Yingrui, Cao Yundi, Dai Lingyun, Wang Jigang, Zhao Pan, Wang Xin, Xiao Zhangang, Qiu Chen, Wang Guang-Suo, Zou Chang

机构信息

Clinical Medical Research Centre, The First Affiliated Hospital, Southern University of Science and Technology, Shenzhen People's Hospital, Shenzhen, China.

Shenzhen Public Service Platform on Tumor Precision Medicine and Molecular Diagnosis, Shenzhen, China.

出版信息

Front Oncol. 2021 Feb 19;10:571521. doi: 10.3389/fonc.2020.571521. eCollection 2020.

Abstract

The clinical significance of mutation in multiple pulmonary nodules is largely limited by single gene mutation-directed analysis and lack of validation of gene expression profiles. New analytic strategy is urgently needed for comprehensive understanding of genomic data in multiple pulmonary nodules. In this study, we performed whole exome sequencing in 16 multiple lung nodules and 5 adjacent normal tissues from 4 patients with multiple pulmonary nodules and decoded the mutation information from a perspective of cellular functions and signaling pathways. Mutated genes as well as mutation patterns shared in more than two lesions were identified and characterized. We found that the number of mutations or mutated genes and the extent of protein structural changes caused by different mutations is positively correlated with the degree of malignancy. Moreover, the mutated genes in the nodules are associated with the molecular functions or signaling pathways related to cell proliferation and survival. We showed a developing pattern of quantity (the number of mutations/mutated genes) and quality (the extent of protein structural changes) in multiple pulmonary nodules. The mutation and mutated genes in multiple pulmonary nodules are associated with cell proliferation and survival related signaling pathways. This study provides a new perspective for comprehension of genomic mutational data and might shed new light on deciphering molecular evolution of early stage lung adenocarcinoma.

摘要

多个肺结节中突变的临床意义在很大程度上受限于单基因突变导向分析以及基因表达谱缺乏验证。迫切需要新的分析策略来全面理解多个肺结节中的基因组数据。在本研究中,我们对4例患有多个肺结节患者的16个多个肺结节及5个相邻正常组织进行了全外显子组测序,并从细胞功能和信号通路的角度解码了突变信息。鉴定并表征了在两个以上病灶中共享的突变基因以及突变模式。我们发现,不同突变引起的突变数量或突变基因数量以及蛋白质结构变化程度与恶性程度呈正相关。此外,结节中的突变基因与细胞增殖和存活相关的分子功能或信号通路有关。我们展示了多个肺结节中数量(突变/突变基因数量)和质量(蛋白质结构变化程度)的发展模式。多个肺结节中的突变和突变基因与细胞增殖和存活相关信号通路有关。本研究为理解基因组突变数据提供了新视角,并可能为解读早期肺腺癌的分子进化带来新的启示。

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