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C3orf21基因缺失促进肺腺癌增殖,其在rs2131877位点的突变可能作为一种易感性标志物。

C3orf21 ablation promotes the proliferation of lung adenocarcinoma, and its mutation at the rs2131877 locus may serve as a susceptibility marker.

作者信息

Yang Litao, Wang Ying, Fang Meiyu, Deng Douhou, Zhang Yongjun

机构信息

Department of Abdominal Surgery, Zhejiang Cancer Hospital, Hangzhou, China.

Department of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China.

出版信息

Oncotarget. 2017 May 16;8(20):33422-33431. doi: 10.18632/oncotarget.16798.

Abstract

In this study, we investigated the role of C3orf21 gene polymorphism at the rs2131877 locus and its contribution to lung adenocarcinoma pathogenesis. Normal lung and tumor tissue sections were collected from fifteen patients with lung adenocarcinoma for chromosome 3 open reading frame 21 (C3orf21) genotype analysis. In addition, a retrospective analysis was performed to assess the association between C3orf21 genotype and tumor markers from patient samples used in our previously published study. In parallel, we also manipulated C3orf21 gene expression either by overexpressing or ablating it in a MSTO-211H human lung cancer cell line to further understand its contribution to cell proliferation, apoptosis and migration. Our results indicated that the patients with smoking history had a significantly increased mutation (rs2131877 T/C+C/C genotype) rate (p = 0.025), in addition to higher values for the CYF211 and NSE tumor markers (p = 0.014 and p = 0.031, respectively). The retrospective analysis also confirmed that the NSE marker value was higher in patients with a C3orf21 rs2131877 T/C+C/C genotype. Furthermore, our in vitro data indicated that C3orf21 ablation promoted lung cancer cell proliferation, inhibited apoptosis and accelerated cell migration. Overall, our study concluded that C30rf21 rs 2131877 T/C+C/C genotype patients may experience increased nicotine addiction and that C30rf21 can likely serve as a susceptibility marker for lung adenocarcinoma with a higher degree of malignancy.

摘要

在本研究中,我们调查了rs2131877位点的C3orf21基因多态性及其在肺腺癌发病机制中的作用。从15例肺腺癌患者中收集正常肺组织和肿瘤组织切片,用于3号染色体开放阅读框21(C3orf21)基因分型分析。此外,进行了一项回顾性分析,以评估C3orf21基因分型与我们之前发表的研究中使用的患者样本中的肿瘤标志物之间的关联。同时,我们还通过在MSTO-211H人肺癌细胞系中过表达或敲除C3orf21基因来调控其基因表达,以进一步了解其对细胞增殖、凋亡和迁移的作用。我们的结果表明,有吸烟史的患者突变(rs2131877 T/C+C/C基因型)率显著增加(p = 0.025),此外CYF211和NSE肿瘤标志物的值更高(分别为p = 0.014和p = 0.031)。回顾性分析还证实,C3orf21 rs2131877 T/C+C/C基因型患者的NSE标志物值更高。此外,我们的体外数据表明,敲除C3orf21可促进肺癌细胞增殖、抑制凋亡并加速细胞迁移。总体而言,我们的研究得出结论,C30rf21 rs 2131877 T/C+C/C基因型患者可能对尼古丁成瘾增加,并且C30rf21可能作为具有更高恶性程度的肺腺癌的易感标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea58/5464879/d948a7e74a21/oncotarget-08-33422-g001.jpg

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