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苯乙烯基喹啉类化合物对人结肠腺癌细胞的化学预防作用:合成、细胞毒性、促凋亡作用及分子对接分析。

Chemopreventive Effect on Human Colon Adenocarcinoma Cells of Styrylquinolines: Synthesis, Cytotoxicity, Proapoptotic Effect and Molecular Docking Analysis.

机构信息

Medical and Experimental Mycology Group, CIB-UPB-UdeA-UDES, Medellin 050034, Colombia.

Chemistry of Colombian Plants Group, Faculty of Exact and Natural Sciences, Institute of Chemistry, University of Antioquia (UdeA), Medellin 050010, Colombia.

出版信息

Molecules. 2022 Oct 21;27(20):7108. doi: 10.3390/molecules27207108.

Abstract

Seven styrylquinolines were synthesized in this study. Two of these styrylquinolines are new and were elucidated by spectroscopic analysis. The chemopreventive potential of these compounds was evaluated against SW480 human colon adenocarcinoma cells, its metastatic derivative SW620, and normal cells (HaCaT). According to the results, compounds and showed antiproliferative activity in SW480 and SW620 cells, but their effect seemed to be caused by different mechanisms of action. Compound induced apoptosis independent of ROS production, as evidenced by increased levels of caspase 3, and had an immunomodulatory effect, positively regulating the production of different immunological markers in malignant cell lines. In contrast, compound generated a pro-oxidant response and inhibited the growth of cancer cells, probably by another type of cell death other than apoptosis. Molecular docking studies indicated that the most active compound, could efficiently bind to the proapoptotic human caspases-3 protein, a result that could provide valuable information on the biochemical mechanism for the in vitro cytotoxic response of this compound in SW620 colon carcinoma cell lines. The obtained results suggest that these compounds have chemopreventive potential against CRC, but more studies should be carried out to elucidate the molecular mechanisms of action of each of them in depth.

摘要

本研究合成了七种苯乙烯基喹啉。其中两种苯乙烯基喹啉是新的,并通过光谱分析进行了阐明。这些化合物的化学预防潜力针对 SW480 人结肠腺癌细胞、其转移性衍生物 SW620 和正常细胞(HaCaT)进行了评估。结果表明,化合物 和 对 SW480 和 SW620 细胞具有增殖抑制活性,但它们的作用似乎是由不同的作用机制引起的。化合物 诱导凋亡不依赖于 ROS 的产生,这一点可以通过 caspase 3 水平的增加来证明,并且具有免疫调节作用,可正向调节恶性细胞系中不同免疫标志物的产生。相比之下,化合物 产生了促氧化剂反应并抑制了癌细胞的生长,可能是通过另一种不同于细胞凋亡的细胞死亡类型。分子对接研究表明,最活跃的化合物 可以有效地与促凋亡的人 caspase-3 蛋白结合,这一结果可以为该化合物在 SW620 结肠癌细胞系中的体外细胞毒性反应的生化机制提供有价值的信息。所得结果表明,这些化合物具有针对 CRC 的化学预防潜力,但应进行更多研究以深入阐明它们各自的作用机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b75/9607578/b210a43df093/molecules-27-07108-g001.jpg

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