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本文引用的文献

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Long non-coding RNAs in gastric cancer: New emerging biological functions and therapeutic implications.长链非编码 RNA 在胃癌中的作用:新的生物学功能和治疗意义。
Theranostics. 2020 Jul 11;10(19):8880-8902. doi: 10.7150/thno.47548. eCollection 2020.
3
A functional polymorphism rs2257440 in the gene regulates its expression via MTF-1 in esophageal squamous cell carcinoma.基因中的一个功能性多态性位点rs2257440通过金属反应元件结合转录因子1(MTF-1)在食管鳞状细胞癌中调节其表达。
Int J Clin Exp Pathol. 2017 Nov 1;10(11):11006-11013. eCollection 2017.
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DcR3 promotes proliferation and invasion of pancreatic cancer via a DcR3/STAT1/IRF1 feedback loop.DcR3通过DcR3/STAT1/IRF1反馈环促进胰腺癌的增殖和侵袭。
Am J Cancer Res. 2019 Dec 1;9(12):2618-2633. eCollection 2019.
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The Chinese Society of Clinical Oncology (CSCO): clinical guidelines for the diagnosis and treatment of gastric cancer.中国临床肿瘤学会(CSCO):胃癌诊断与治疗临床实践指南。
Cancer Commun (Lond). 2019 Mar 18;39(1):10. doi: 10.1186/s40880-019-0349-9.
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Subgrouping breast cancer patients based on immune evasion mechanisms unravels a high involvement of transforming growth factor-beta and decoy receptor 3.基于免疫逃逸机制对乳腺癌患者进行亚组分类,揭示转化生长因子-β和诱饵受体 3 的高参与度。
PLoS One. 2018 Dec 4;13(12):e0207799. doi: 10.1371/journal.pone.0207799. eCollection 2018.
7
Risk Prediction of Prostate Cancer with Single Nucleotide Polymorphisms and Prostate Specific Antigen.利用单核苷酸多态性和前列腺特异性抗原预测前列腺癌风险
J Urol. 2019 Mar;201(3):486-495. doi: 10.1016/j.juro.2018.10.015.
8
The siRNA silencing of DcR3 expression induces Fas ligand-mediated apoptosis in HepG2 cells.DcR3表达的小干扰RNA沉默诱导HepG2细胞中Fas配体介导的凋亡。
Exp Ther Med. 2018 May;15(5):4370-4378. doi: 10.3892/etm.2018.5964. Epub 2018 Mar 19.
9
Progress in the treatment of advanced gastric cancer.晚期胃癌治疗的进展
Tumour Biol. 2017 Jul;39(7):1010428317714626. doi: 10.1177/1010428317714626.
10
DcR3, TFF3, and Midkine Are Novel Serum Biomarkers in Small Intestinal Neuroendocrine Tumors.DcR3、TFF3和中期因子是小肠神经内分泌肿瘤中的新型血清生物标志物。
Neuroendocrinology. 2017;105(2):170-181. doi: 10.1159/000452891. Epub 2016 Nov 9.

中国汉族人群基因多态性与胃癌易感性的病例对照研究

Case-Control Study on Gene Polymorphism and Susceptibility to Gastric Cancer in a Chinese Han Population.

作者信息

Gu Xuyu, Mao Zhenwei, Pan Huiwen, Zou Chen, Ding Guowen, Fan Yu

机构信息

School of Medicine, Southeast University, Nanjing, Jiangsu 210009, People's Republic of China.

Cancer Institute, Affiliated People's Hospital of Jiangsu University, Zhenjiang, Jiangsu 212002, People's Republic of China.

出版信息

Pharmgenomics Pers Med. 2020 Dec 17;13:749-756. doi: 10.2147/PGPM.S283308. eCollection 2020.

DOI:10.2147/PGPM.S283308
PMID:33363398
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7751833/
Abstract

PURPOSE

To explore the relationship between rs2297440 and rs2297441 polymorphisms of gene and susceptibility to gastric cancer.

METHODS

A hospital-based case-control study was conducted. A total of 577 gastric cancer cases and 678 normal controls were recruited. Their genotypes were determined using the SnapShot method.

RESULTS

The smoking rate in the case group (34.49%) was higher than that in the control group (27.29%). For rs2297440, among people <62 years old, the risk of gastric cancer in TC people was 1.84 times that in TT people. Among the non-drinking people, the risk of gastric cancer in the CC type was 0.66 times that in the TT+TC type. Among the drinking population, the risk of gastric cancer in the TC type was 1.67 times that in the TT type, and the risk in the TC+CC type was 1.70 times that in the TT type. As for rs2297441, in males and non-drinkers, the risk of gastric cancer in the AG type was less than that in the GG type. No matter how old the patient is, the risk of gastric cancer in the AA type was less than that in the AG+GG type.

CONCLUSION

A correlation exists between smoking and gastric cancer. For rs2297440, the TC genotype may be a risk factor for gastric cancer in people <62 years old. In the non-drinking population, the homozygous mutant of CC may be a protective factor for gastric cancer. In the drinking population, TC type may be a risk factor, whereas the TC+CC type dominated by C may be a protective factor. For rs2297441, the AG genotype may be a risk factor for gastric cancer in males and non-drinkers. The AA homozygous mutant may be a protective factor for gastric cancer.

摘要

目的

探讨基因的rs2297440和rs2297441多态性与胃癌易感性之间的关系。

方法

开展一项基于医院的病例对照研究。共招募了577例胃癌病例和678例正常对照。采用荧光微球技术测定他们的基因型。

结果

病例组的吸烟率(34.49%)高于对照组(27.29%)。对于rs2297440,在62岁以下人群中,TC型人群患胃癌的风险是TT型人群的1.84倍。在不饮酒人群中,CC型患胃癌的风险是TT+TC型的0.66倍。在饮酒人群中,TC型患胃癌的风险是TT型的1.67倍,TC+CC型的风险是TT型的1.70倍。至于rs2297441,在男性和不饮酒者中,AG型患胃癌的风险低于GG型。无论患者年龄多大,AA型患胃癌的风险低于AG+GG型。

结论

吸烟与胃癌之间存在相关性。对于rs2297440,TC基因型可能是62岁以下人群患胃癌的危险因素。在不饮酒人群中,CC的纯合突变可能是胃癌的保护因素。在饮酒人群中,TC型可能是危险因素,而以C为主的TC+CC型可能是保护因素。对于rs2297441,AG基因型可能是男性和不饮酒者患胃癌的危险因素。AA纯合突变可能是胃癌的保护因素。