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新型丙烯酸酯衍生物作为潜在抗癌剂的设计、合成及抗增殖筛选

Design, synthesis and antiproliferative screening of newly synthesized acrylate derivatives as potential anticancer agents.

作者信息

Alshaya Dalal Sulaiman, Tawakul Rana M O, Zaki Islam, Abu Almaaty Ali H, Fayad Eman, Abd El-Aziz Yasmin M

机构信息

Department of Biology, College of Science, Princess Nourah bint Abdulrahman University P.O. Box 84428 Riyadh 11671 Saudi Arabia.

Zoology Department, Faculty of Science, Port Said University Port Said 42526 Egypt.

出版信息

RSC Adv. 2023 Aug 4;13(34):23538-23546. doi: 10.1039/d3ra03849a.

Abstract

A new series of acrylic acid and acrylate ester derivatives as modified analogs of tubulin polymerization inhibitors were designed and synthesized. The antiproliferative activity of the constructed molecules was investigated against MCF-7 breast carcinoma cells using CA-4 as positive molecule. Methyl acrylate ester 6e emerged as the most potent cytotoxic agent against MCF-7 cells, with an IC value of 2.57 ± 0.16 μM. Also, methyl acrylate ester molecule 6e showed good β-tubulin polymerization inhibition activity. Cellular cycle analysis showed that compound 6e can arrest MCF-7 cells at the G2/M phase. In addition, this compound produced a significant increase in apoptotic power as compared to control untreated MCF-7 cells. Furthermore, the effect of acrylate ester 6e on the gene expression levels of p53, Bax and Bcl-2 was investigated. This molecule increased the expression levels of both p53 and Bax, and decreased the gene expression level of Bcl-2 as compared to control untreated MCF-7 carcinoma cells.

摘要

设计并合成了一系列新型丙烯酸和丙烯酸酯衍生物,作为微管蛋白聚合抑制剂的修饰类似物。以CA-4为阳性对照分子,研究了所构建分子对MCF-7乳腺癌细胞的抗增殖活性。丙烯酸甲酯6e对MCF-7细胞表现出最强的细胞毒性,IC值为2.57±0.16μM。此外,丙烯酸甲酯分子6e显示出良好的β-微管蛋白聚合抑制活性。细胞周期分析表明,化合物6e可使MCF-7细胞停滞于G2/M期。此外,与未处理的对照MCF-7细胞相比,该化合物的凋亡能力显著增强。此外,还研究了丙烯酸酯6e对p53、Bax和Bcl-2基因表达水平的影响。与未处理的对照MCF-7癌细胞相比,该分子增加了p53和Bax的表达水平,并降低了Bcl-2的基因表达水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6ab/10402871/2b22778632d3/d3ra03849a-f1.jpg

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