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口服避孕药的使用可能会调节全基因组DNA甲基化以及APC1和ESR1的启动子甲基化。

Oral Contraceptive Use May Modulate Global Genomic DNA Methylation and Promoter Methylation of APC1 and ESR1.

作者信息

Moradi Sarabi Mostafa, Ghareghani Parvin, Khademi Fatemeh, Zal Fatemeh

机构信息

Biochemistry and Genetics Department, Faculty of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran. Email:

出版信息

Asian Pac J Cancer Prev. 2017 Sep 27;18(9):2361-2366. doi: 10.22034/APJCP.2017.18.9.2361.

Abstract

Background: There are challenging reports in the public health sphere regarding associations between oral contraceptive (OC) use and cancer risk. Methods: To evaluate possible effects of OCs on cancer susceptibility, we quantified of global 5-methyl cytosine (5-mC) levels and assessed methylation patterns of CpG islands of two key tumor suppressor genes, APC1 and ESR1, in serum of users by enzyme-linked immunosorbent assay and methylation specific PCR methods, respectively. Results: Our results indicated that OCs significantly decrease the level of global DNA methylation in users relative to control non-users. However, our data revealed no significant differences between CpG island methylation patterns for ESR1 and APC1 in healthy control and OC-treated women. However, we did find a trend for hypermethylation of both tumor suppressor genes in OC users. Conclusion: Our data suggest that the level of 5-mC but not individual CpG island patterns is significantly influenced by OCs in our cross-section of adult users.

摘要

背景

在公共卫生领域,关于口服避孕药(OC)使用与癌症风险之间的关联存在具有挑战性的报告。方法:为了评估OC对癌症易感性的可能影响,我们分别通过酶联免疫吸附测定法和甲基化特异性PCR方法,对使用者血清中整体5-甲基胞嘧啶(5-mC)水平进行了定量,并评估了两个关键肿瘤抑制基因APC1和ESR1的CpG岛的甲基化模式。结果:我们的结果表明,与未使用OC的对照者相比,OC使用者的整体DNA甲基化水平显著降低。然而,我们的数据显示,健康对照者和接受OC治疗的女性中,ESR1和APC1的CpG岛甲基化模式没有显著差异。不过,我们确实发现OC使用者中这两个肿瘤抑制基因均有高甲基化的趋势。结论:我们的数据表明,在我们的成年使用者样本中,OC显著影响5-mC水平,但不影响单个CpG岛模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87ee/5720637/fc214b4793cd/APJCP-18-2361-g001.jpg

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