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本文引用的文献

1
Prognostic and Predictive Value of /Cyclin D1 Amplification in Breast Cancer With a Focus on Postmenopausal Patients: A Systematic Review and Meta-Analysis.Cyclin D1 扩增在乳腺癌中的预后和预测价值:一项基于绝经后患者的系统评价和荟萃分析。
Front Endocrinol (Lausanne). 2022 Jun 17;13:895729. doi: 10.3389/fendo.2022.895729. eCollection 2022.
2
Breast Cancer Survival and Incidence: 10 Years Cancer Registry Data in the Northwest, Iran.乳腺癌生存率与发病率:伊朗西北部癌症登记处10年数据
Int J Breast Cancer. 2020 May 1;2020:1963814. doi: 10.1155/2020/1963814. eCollection 2020.
3
Re-evaluating genetic variants identified in candidate gene studies of breast cancer risk using data from nearly 280,000 women of Asian and European ancestry.利用近 28 万名亚洲和欧洲血统女性的数据,重新评估乳腺癌风险候选基因研究中发现的遗传变异。
EBioMedicine. 2019 Oct;48:203-211. doi: 10.1016/j.ebiom.2019.09.006. Epub 2019 Oct 16.
4
Association of CCND1 Gene c.870G>A Polymorphism with Breast Cancer Risk: A Case-ControlStudy and a Meta-Analysis.CCND1基因c.870G>A多态性与乳腺癌风险的关联:一项病例对照研究及荟萃分析
Pathol Oncol Res. 2017 Jul;23(3):621-631. doi: 10.1007/s12253-016-0165-3. Epub 2016 Dec 21.
5
Association Between Polymorphism rs678653 in Human Cyclin D1 Gene (CCND1) and Susceptibility to Cancer: A Meta-Analysis.人类细胞周期蛋白D1基因(CCND1)多态性rs678653与癌症易感性的关联:一项荟萃分析。
Med Sci Monit. 2016 Mar 16;22:863-74. doi: 10.12659/msm.895237.
6
The significant association of CCND1 genotypes with colorectal cancer in Taiwan.CCND1基因分型与台湾地区结直肠癌的显著关联。
Tumour Biol. 2015 Aug;36(8):6533-40. doi: 10.1007/s13277-015-3347-9. Epub 2015 Mar 26.
7
Cyclin D1, Id1 and EMT in breast cancer.细胞周期蛋白 D1、Id1 和 EMT 在乳腺癌中的作用。
BMC Cancer. 2011 Sep 28;11:417. doi: 10.1186/1471-2407-11-417.

伊朗乳腺癌易感性与细胞周期蛋白D1单核苷酸多态性相关:一项病例对照研究。

Breast cancer susceptibility is associated with Cyclin D1 single nucleotide polymorphisms in Iran: A case-control study.

作者信息

Soleimani Sadaf, Talesh Sasani Soheila, Salehi Zivar, Fakour Fereshteh

机构信息

Department of Biology, Faculty of Sciences, University of Guilan, Rasht, Iran.

Medicine School, Guilan Medical University, Rasht, Iran.

出版信息

Mol Biol Res Commun. 2025;14(3):199-202. doi: 10.22099/mbrc.2025.51763.2065.

DOI:10.22099/mbrc.2025.51763.2065
PMID:40321701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12046365/
Abstract

Breast cancer (BC) is the main cause of cancer-related death in women worldwide. We evaluated the association between the key gene variant; rs9344 (G>A); and BC risk in Iran. In this case-control study, blood samples were obtained from 58 patients and 66 healthy controls. Genotyping was conducted by tetra-primer amplification refractory mutation system PCR (T-ARMS-PCR). Statistical analysis was performed by MedCalc software. Our results showed that the polymorphism rs9344 has an association with BC risk in the Iranian population. Based on the codominant and recessive models, carriers of the AA genotype are nearly 3.5 times more susceptible to BC than other individuals, and the AA genotype of A870G may be a significant factor for breast cancer. Further studies are needed to clarify the roles of polymorphism, rs9344, in breast cancer.

摘要

乳腺癌(BC)是全球女性癌症相关死亡的主要原因。我们评估了关键基因变异rs9344(G>A)与伊朗人群患BC风险之间的关联。在这项病例对照研究中,采集了58例患者和66例健康对照者的血样。采用四引物扩增阻滞突变系统PCR(T-ARMS-PCR)进行基因分型。使用MedCalc软件进行统计分析。我们的结果表明,多态性rs9344与伊朗人群患BC的风险相关。基于共显性和隐性模型,AA基因型携带者患BC的易感性比其他个体高近3.5倍,A870G的AA基因型可能是乳腺癌的一个重要因素。需要进一步研究来阐明多态性rs9344在乳腺癌中的作用。