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白藜芦醇通过调节线粒体和PI3K/AKT信号通路对小鼠皮肤肿瘤的化学预防潜力。

Chemopreventive potential of resveratrol in mouse skin tumors through regulation of mitochondrial and PI3K/AKT signaling pathways.

作者信息

Roy Preeti, Kalra Neetu, Prasad Sahdeo, George Jasmine, Shukla Yogeshwer

机构信息

Proteomics Laboratory, Indian Institute of Toxicology Research, (Council of Scientific & Industrial Research, India), P.O. Box 80, M.G. Marg, Lucknow, 226001, India.

出版信息

Pharm Res. 2009 Jan;26(1):211-7. doi: 10.1007/s11095-008-9723-z. Epub 2008 Sep 13.

Abstract

PURPOSE

To investigate the chemopreventive potential of resveratrol, a phytoalexin found in seeds and skin of grapes, berries and peanuts in 7,12 dimethyl benz(a)anthracene (DMBA) induced mouse skin tumorigenesis.

METHODS

Topical treatment of resveratrol was given to the animals 1 h prior to DMBA for 28 weeks. At the end of the study period, the skin tumors were dissected out and western blotting was carried out to examine the regulation of proteins involved in anti-tumorigenesis in response to resveratrol.

RESULTS

Chemopreventive properties of resveratrol were reflected by delay in onset of tumorigenesis, reduced cumulative number of tumors, and reduction in tumor volume. Results of the western blotting showed that resveratrol treatment increased the DMBA suppressed p53 and Bax while decreased the expression of Bcl-2 and Survivin. Further, resveratrol supplementation resulted in release of cytochrome C, caspases activation, increase in apoptotic protease-activating factor-1 (Apaf-1) as mechanism of apoptosis induction. Resveratrol was also found to inhibit skin tumorigenesis through regulation of Phosphatidylinositol-3-kinase (PI3K)/ and AKT proteins which are implicated in cancer progression because it stimulates proliferation and suppresses apoptosis.

CONCLUSIONS

Based on the results we can conclude that resveratrol regulates apoptosis and cell survival in mouse skin tumors as mechanism of chemoprevention hence deserve to be a chemopreventive agent.

摘要

目的

研究白藜芦醇(一种存在于葡萄种子、葡萄皮、浆果和花生中的植物抗毒素)在7,12-二甲基苯并(a)蒽(DMBA)诱导的小鼠皮肤肿瘤发生过程中的化学预防潜力。

方法

在给予DMBA前1小时对动物进行白藜芦醇局部治疗,持续28周。在研究期结束时,取出皮肤肿瘤并进行蛋白质印迹分析,以检测白藜芦醇对参与抗肿瘤发生的蛋白质的调节作用。

结果

白藜芦醇的化学预防特性表现为肿瘤发生起始延迟、肿瘤累积数量减少以及肿瘤体积减小。蛋白质印迹分析结果显示,白藜芦醇治疗可增加DMBA抑制的p53和Bax,同时降低Bcl-2和Survivin的表达。此外,补充白藜芦醇可导致细胞色素C释放、半胱天冬酶激活以及凋亡蛋白酶激活因子-1(Apaf-1)增加,这是诱导凋亡的机制。还发现白藜芦醇通过调节磷脂酰肌醇-3-激酶(PI3K)/AKT蛋白抑制皮肤肿瘤发生,PI3K/AKT蛋白与癌症进展有关,因为它刺激增殖并抑制凋亡。

结论

基于这些结果我们可以得出结论,白藜芦醇调节小鼠皮肤肿瘤中的凋亡和细胞存活,作为化学预防机制,因此值得作为一种化学预防剂。

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