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Synthesis of Combretastatin A-4 and 3′-Aminocombretastatin A-4 derivatives with Aminoacid Containing Pendants and Study of their Interaction with Tubulin and as Downregulators of the VEGF hTERT and c-Myc Gene Expression

机译:含氨基酸侧链的Combretastatin A-4和3-Aminocombretastatin A-4衍生物的合成及其与微管蛋白的相互作用以及作为VEGFhTERT和c-Myc基因表达下调剂的相互作用的研究

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摘要

Natural product combretastatin A-4 (CA-4) and its nitrogenated analogue 3′-aminocombretastatin A-4 (AmCA-4) have shown promising antitumor activities. In this study, a range of CA-4 and AmCA-4 derivatives containing amino acid pendants have been synthesized in order to compare their biological actions with those of their parent compounds. Thus, inhibition of cell proliferation on tumor cell lines HT-29, MCF-7 and A-549, as well as on the nontumor cell line HEK-273; in vitro tubulin polymerization; mitotic cell arrest; action on the microtubule cell network and inhibition of , and genes have been evaluated. Some AmCA-4 derivatives bearing L-amino acids exhibited inhibition of cell proliferation at low nanomolar levels exceeding the values shown by AmCA-4. Furthermore, while CA-4 and AmCA-4 derivatives do not show significant effects on the in vitro tubulin polymerization and cell cycle arrest, some selected CA-4 and AmCA-4 derivatives are able to cause total depolymerization of the microtubule network on A-549 cells. The best results were obtained in the inhibition of gene expression, particularly on the gene, in which some AmCA-4 derivatives greatly exceeded the inhibition values achieved by the parent compound.
机译:天然产品康普他汀A-4(CA-4)及其硝化类似物3'-aminocombretastatin A-4(AmCA-4)已显示出有希望的抗肿瘤活性。在这项研究中,合成了一系列含有氨基酸侧基的CA-4和AmCA-4衍生物,以便将其生物学活性与其母体化合物进行比较。因此,抑制肿瘤细胞HT-29,MCF-7和A-549以及非肿瘤细胞HEK-273上的细胞增殖;体外微管蛋白聚合;有丝分裂细胞停滞;已评估了对微管细胞网络的作用以及对和的抑制作用。一些带有L-氨基酸的AmCA-4衍生物在低纳摩尔水平上显示出对细胞增殖的抑制作用,超过了AmCA-4所示的值。此外,虽然CA-4和AmCA-4衍生物对体外微管蛋白聚合和细胞周期停滞没有显着影响,但某些选定的CA-4和AmCA-4衍生物能够引起A-上的微管网络完全解聚。 549个细胞。在抑制基因表达,特别是抑制基因表达方面获得了最佳结果,其中某些AmCA-4衍生物大大超过了母体化合物所达到的抑制值。

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