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β-榄香烯作为一种抗肿瘤因子,下调 survivin、Bcl-xL 和 Mta-1 的表达。

β-elemene acts as an antitumor factor and downregulates the expression of survivin, Bcl-xL and Mta-1.

机构信息

Department of Urology, the Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, PR China.

出版信息

Mol Med Rep. 2012 Nov;6(5):989-95. doi: 10.3892/mmr.2012.1018. Epub 2012 Aug 3.

Abstract

β-elemene, a non-cellular antineoplastic agent, may be used to effectively inhibit the growth and proliferation of various types of tumor cells by inhibiting the nucleic acid synthesis or inducing their apoptosis and differentiation. The aim of this study was to investigate the expression, as well as the effects, of Mta-1, survivin and Bcl-xL in T24 bladder cancer cells following β-elemene treatment. The expression of the three proteins in T24 cells following β-elemene treatment was analyzed by immunocytochemistry staining and western blot analysis. The survival rate and apoptosis of T24 cells following β-elemene treatment was detected by MTT assay and TUNEL staining. We analyzed the internal corelations between apoptosis-associated genes, tumor metastasis-associated genes (cancer genes) and cell apoptosis, and investigated the mechanism of action by which β-elemene induces the apoptosis of T24 cells at a molecular level. These results provide scientific evidence for further study on the anticancer effect of β-elemene in carcinoma of the urinary bladder. In this study, it is shown that β-elemene downregulates the expression of survivin, Bcl-xL and Mta-1 in tumor cells. The apoptosis of T24 cells is dependent on the dosage and length of incubation time of β-elemene.

摘要

β-榄香烯是一种非细胞抗肿瘤药物,通过抑制核酸合成或诱导肿瘤细胞凋亡和分化,可能有效地抑制各种类型的肿瘤细胞的生长和增殖。本研究旨在探讨β-榄香烯处理后 T24 膀胱癌细胞中 Mta-1、survivin 和 Bcl-xL 的表达及其作用。采用免疫细胞化学染色和 Western blot 分析β-榄香烯处理后 T24 细胞中这三种蛋白的表达。采用 MTT 法和 TUNEL 染色检测β-榄香烯处理后 T24 细胞的存活率和凋亡。分析凋亡相关基因、肿瘤转移相关基因(癌基因)与细胞凋亡之间的内在相关性,并从分子水平上探讨β-榄香烯诱导 T24 细胞凋亡的作用机制。这些结果为进一步研究β-榄香烯在膀胱癌中的抗癌作用提供了科学依据。本研究表明,β-榄香烯下调肿瘤细胞中 survivin、Bcl-xL 和 Mta-1 的表达。T24 细胞的凋亡依赖于β-榄香烯的剂量和孵育时间的长短。

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