Research Papers:

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

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

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Oncotarget. 2017; 8:33422-33431. https://doi.org/10.18632/oncotarget.16798

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Litao Yang1,*, Ying Wang2,*, Meiyu Fang3, Douhou Deng3, Yongjun Zhang3

1Department of Abdominal Surgery, Zhejiang Cancer Hospital, Hangzhou, China

2Department of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China

3Department of Integration of Traditional Chinese and Western Medicine, Zhejiang Cancer Hospital, Hangzhou, China

* These authors contributed equally to this work and are co-first authors

Correspondence to:

Yongjun Zhang, email: zhangyj@zjcc.org.cn

Keywords: C3orf21, cell apoptosis, cell migration, lung adenocarcinoma, polysaccharide modification

Received: January 18, 2017     Accepted: March 24, 2017     Published: April 03, 2017


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.

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