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Evaluation of heterocyclic steroids and curcumin derivatives as anti breast cancer agents: Studying the effect on apoptosis in MCF-7 breast cancer cells

机译:杂环类固醇和姜黄素衍生物作为抗乳腺癌药物的评估:研究对MCF-7乳腺癌细胞凋亡的影响

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摘要

Anticancer agents consisting of hybrid molecules are used to improve effectiveness and diminish drug resistance. The current study aimed to introduce newly synthesized hetero-steroids of promising anticancer effects. Besides, the pro-apoptotic effects of new compounds were investigated extensively. Several pyrimidino-, triazolopyrimidino-, pyridazino-, and curcumin-steroid derivatives were synthesized, elucidated and confirmed using the spectral and analytical data. The synthesized hetero-steroids, compounds 9, 10, 11, 12, 13, 14, 15, 18, 20, 21, 22 and 24, were tested for their cytotoxic effects versus human breast cancer cells (MCF-7) using neutral red supravital dye uptake assay. Compound 24 (IC50 = 18 mu M) showed more inhibitory influence on MCF-7 growth. Using QRT-PCR (Quantitative real time-polymerase chain reaction), CCND1, Survivin, BCL-2, CDC2, P21 and P53, genes expression levels were investigated. The study results disclose that compounds 4, 7, 18, 24 knocked down the expression levels of CCND1, Survivin, BCL-2 and CDC2. However, P21 and P53 were up-regulated by compounds 21, 22. This study introduced promising pro-apoptotic anticancer agents acting through the modulation of key regulators of apoptosis and cell cycle genes. (C) 2016 Elsevier Inc. All rights reserved.
机译:由杂种分子组成的抗癌药可用于提高疗效并降低耐药性。目前的研究旨在介绍具有抗癌作用的新合成的杂类固醇。此外,广泛研究了新化合物的促凋亡作用。使用光谱和分析数据合成,阐明和确认了几种嘧啶基,三唑并嘧啶基,哒嗪基和姜黄素类固醇衍生物。使用中性红测试了合成的杂类固醇化合物9、10、11、12、13、14、15、18、20、21、22和24对人乳腺癌细胞(MCF-7)的细胞毒性作用上染料摄取分析。化合物24(IC50 = 18μM)对MCF-7的生长表现出更多的抑制作用。使用QRT-PCR(实时定量定量聚合酶链反应),CCND1,Survivin,BCL-2,CDC2,P21和P53,研究基因表达水平。研究结果表明,化合物4、7、18、24降低了CCND1,Survivin,BCL-2和CDC2的表达水平。但是,P21和P53被化合物21、22上调。该研究引入了有前途的促凋亡抗癌药,其作用是通过调节细胞凋亡和细胞周期基因的关键调控因子来发挥作用。 (C)2016 Elsevier Inc.保留所有权利。

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