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阿特洛帕提纳玄参提取物可逆转乳腺癌细胞中TP53基因启动子的高甲基化并降低生存素抗凋亡基因的表达。

Scrophularia Atropatana Extract Reverses TP53 Gene Promoter Hypermethylation and Decreases Survivin Antiapoptotic Gene Expression in Breast Cancer Cells.

作者信息

Ghavifekr Fakhr Mehrdad, Rezaie Kahkhaie Kolsoum, Shanehbandi Dariush, Farshdousti Hagh Majid, Zarredar Habib, Safarzadeh Elham, Abdolrahimi Vind Mina, Baradaran Behzad

机构信息

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Student Research Committee,Zabol University of Medical Science, Zabol, Iran. Email:

出版信息

Asian Pac J Cancer Prev. 2018 Sep 26;19(9):2599-2605. doi: 10.22034/APJCP.2018.19.9.2599.

Abstract

Background: In many cases of breast cancer, the aberrant methylation of TP53 gene leads to uncontrolled cell proliferation and apoptosis inhibition. Moreover, expression of oncogenes which are under the control of P53 protein could be altered. Survivin as a conspicuous example of this category plays important roles in tumorigenesis, drug resistance and apoptosis inhibition. The present study was done to reveal the effects of Scrophularia atropatana extract on epigenetic situation of TP53 gene promoter and the expression levels of anti-apoptotic gene, survivin and its potential for production of cancer epi-drugs. Methods: Cytotoxic effect of dichloromethane extracts of Scrophularia plant on MCF-7 cell line was assessed in our previous study. Cell death ELISA (enzyme-linked immunosorbent assay) and TUNEL (Terminal deoxynucleotidyl transferase dUTP nick end labeling) tests were used to investigate the occurrence of apoptosis in the treated cells. Methylation Specific PCR (MSP) was employed to assess the changes in methylation status of the TP53 gene promoter. Furthermore, quantitative real time PCR was utilized to evaluate the resulting changes in TP53 and survivin genes expression. Results: Cell death ELISA and TUNEL assays confirmed the occurrence of apoptosis. MSP test revealed a significant change in the methylation status of TP53 promoter. QRT-PCR showed an increased TP53 gene expression in the treated cells while a significant decrease in survivin mRNA was evident. Conclusions: According to the outcomes, dichloromethane extract of S. atropatana returned the TP53 gene promoter hypermethylation to normal state. This plant could be a promising source for production of epi-drugs due to its apoptotic effects and reversal of TP53 epigenetic alterations.

摘要

背景

在许多乳腺癌病例中,TP53基因的异常甲基化会导致细胞增殖失控和细胞凋亡抑制。此外,受P53蛋白调控的癌基因表达可能会发生改变。生存素作为这类基因的一个显著例子,在肿瘤发生、耐药性和细胞凋亡抑制中发挥着重要作用。本研究旨在揭示玄参提取物对TP53基因启动子表观遗传状态、抗凋亡基因生存素表达水平的影响及其产生癌症表观遗传药物的潜力。方法:在我们之前的研究中评估了玄参二氯甲烷提取物对MCF-7细胞系的细胞毒性作用。使用细胞死亡ELISA(酶联免疫吸附测定)和TUNEL(末端脱氧核苷酸转移酶dUTP缺口末端标记)试验来研究处理后细胞中凋亡的发生情况。采用甲基化特异性PCR(MSP)评估TP53基因启动子甲基化状态的变化。此外,利用定量实时PCR评估TP53和生存素基因表达的相应变化。结果:细胞死亡ELISA和TUNEL试验证实了细胞凋亡的发生。MSP试验显示TP53启动子的甲基化状态有显著变化。定量逆转录PCR显示处理后细胞中TP53基因表达增加,而生存素mRNA明显减少。结论:根据结果,玄参的二氯甲烷提取物使TP53基因启动子的高甲基化恢复到正常状态。由于其凋亡作用和TP53表观遗传改变的逆转,这种植物可能是生产表观遗传药物的一个有前景的来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7b4/6249477/59b4871bfbf5/APJCP-19-2599-g001.jpg

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