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腺苷A1受体调节乳腺癌细胞系Mcf-7中的P53表达和细胞凋亡。

Adenosine A1 receptor modifies P53 expression and apoptosis in breast cancer cell line Mcf-7.

作者信息

Dastjerdi M Nikbakht, Valiani A, Mardani M, Ra M Zamani

出版信息

Bratisl Lek Listy. 2016;117(4):242-6. doi: 10.4149/bll_2016_046.

Abstract

BACKGROUND

Breast cancer cells over-express the adenosine receptor A1 and in most of these cells, P53 gene is a wild type. Because of this finding and relationship between A1 receptor and cell apoptosis and proliferation, this study aimed to determine the effect of agonist and antagonist of A1 receptor on cell apoptosis and proliferation and recognize the relationship between this receptor and P53 expression.

METHODS

We used a Real-Time PCR test for measuring expression of p53 gene also flow cytometry assay for apoptotic and survival cell rate after treatment of MCF-7 cells with A1 receptor agonist CPA (N6-Cyclopentyladenosine) and A1 receptor antagonist DPCPX (1,3-dipropyl-8-cyclopentylxanthine) in 24,48 and 72 hours.

RESULTS

Our flow cytometry findings indicate that DPCPX significantly induces apoptosis in MCF-7. Also the expression of P53 becomes upregulated with time of DPCPX treatment. CPA treatment increased the survival cell rate and down-regulated this apoptosis-relevant gene P53 (p > 0.05).

CONCLUSION

DPCPX can induce P53 expression which consequently promotes the cell apoptosis in MCF-7. Therefore, DPCPX could be used as an anti-cancer agent (Tab. 1, Fig. 3, Ref. 5).

摘要

背景

乳腺癌细胞过度表达腺苷A1受体,且在这些细胞中的大多数,P53基因是野生型。基于这一发现以及A1受体与细胞凋亡和增殖之间的关系,本研究旨在确定A1受体激动剂和拮抗剂对细胞凋亡和增殖的影响,并明确该受体与P53表达之间的关系。

方法

我们使用实时聚合酶链反应检测法来测量p53基因的表达,同时采用流式细胞术检测在用A1受体激动剂CPA(N6-环戊基腺苷)和A1受体拮抗剂DPCPX(1,3-二丙基-8-环戊基黄嘌呤)处理MCF-7细胞24、48和72小时后的凋亡细胞率和存活细胞率。

结果

我们的流式细胞术研究结果表明,DPCPX可显著诱导MCF-7细胞凋亡。此外,随着DPCPX处理时间的延长,P53的表达上调。CPA处理可提高存活细胞率,并下调这种与凋亡相关的基因P53(p>0.05)。

结论

DPCPX可诱导P53表达,从而促进MCF-7细胞凋亡。因此,DPCPX可作为一种抗癌药物(表1,图3,参考文献5)。

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