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白藜芦醇通过细胞周期阻滞使乳腺癌细胞对美法仑增敏。

Resveratrol chemosensitizes breast cancer cells to melphalan by cell cycle arrest.

机构信息

Universidade Federal do Rio de Janeiro, Instituto de Bioquímica Médica, Rio de Janeiro, RJ 21941-590, Brazil.

出版信息

J Cell Biochem. 2012 Aug;113(8):2586-96. doi: 10.1002/jcb.24134.

Abstract

Melphalan (MEL) is a chemotherapeutic agent used in breast cancer therapy; however, MEL's side effects limit its clinical applications. In the last 20 years, resveratrol (RSV), a polyphenol found in grape skins, has been proposed to reduce the risk of cancer development. The aim of this study was to investigate whether RSV would be able to enhance the antitumor effects of MEL in MCF-7 and MDA-MB-231 cells. RSV potentiated the cytotoxic effects of MEL in human breast cancer cells. This finding was related to the ability of RSV to sensitize MCF-7 cells to MEL-induced apoptosis. The sensitization by RSV involved the enhancement of p53 levels, the decrease of procaspase 8 and the activation of caspases 7 and 9. Another proposed mechanism for the chemosensitization effect of MCF-7 cells to MEL by RSV was the cell cycle arrest in the S phase. The treatment with RSV or MEL increased the levels of p-Chk2. The increase became pronounced in the combined treatments of the compounds. The expression of cyclin A was decreased by treatment with RSV and by the combination of RSV with MEL. While the levels of cyclin dependent kinase 2 (CDK2) remained unchanged by treatments, its active form (Thr(160) -phosphorylated CDK2) was decreased by treatment with RSV and by the combination of RSV with MEL. The activity of CDK7, kinase that phosphorylates CDK2 at Thr(160), was inhibited by RSV and by the combination of RSV with MEL. These results indicate that RSV could be used as an adjuvant agent during breast cancer therapy with MEL.

摘要

美法仑(MEL)是一种用于乳腺癌治疗的化疗药物;然而,MEL 的副作用限制了其临床应用。在过去的 20 年中,白藜芦醇(RSV),一种在葡萄皮中发现的多酚,已被提议用于降低癌症发展的风险。本研究的目的是研究 RSV 是否能够增强 MEL 在 MCF-7 和 MDA-MB-231 细胞中的抗肿瘤作用。RSV 增强了 MEL 在人乳腺癌细胞中的细胞毒性作用。这一发现与 RSV 使 MCF-7 细胞对 MEL 诱导的细胞凋亡敏感的能力有关。RSV 的敏化作用涉及到 p53 水平的增强、前半胱氨酸蛋白酶 8 的减少和半胱天冬酶 7 和 9 的激活。RSV 增强 MCF-7 细胞对 MEL 的化疗增敏作用的另一个可能机制是细胞周期在 S 期停滞。用 RSV 或 MEL 处理会增加 p-Chk2 的水平。在两种化合物的联合处理中,这种增加变得明显。用 RSV 处理和用 RSV 与 MEL 的联合处理会降低 cyclin A 的表达。虽然用治疗处理不会改变 cyclin 依赖激酶 2(CDK2)的水平,但它的活性形式(Thr(160) -磷酸化 CDK2)会被 RSV 处理和 RSV 与 MEL 的联合处理所降低。CDK7 的活性,即磷酸化 CDK2 的 Thr(160)的激酶,被 RSV 和 RSV 与 MEL 的联合抑制。这些结果表明,RSV 可作为乳腺癌治疗中与 MEL 联合应用的辅助剂。

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