首页> 外文期刊>Journal of Medicinal Chemistry >Guanidino anthrathiophenediones as G-quadruplex binders: Uptake, intracellular localization, and anti-Harvey-ras gene activity in bladder cancer cells
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Guanidino anthrathiophenediones as G-quadruplex binders: Uptake, intracellular localization, and anti-Harvey-ras gene activity in bladder cancer cells

机译:胍基蒽噻吩作为G-四链体结合物:膀胱癌细胞的摄取,细胞内定位和抗Harvey-ras基因活性

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摘要

We prepared a series of anthrathiophenediones (ATPDs) with guanidino-alkyl side chains of different length (compounds 1, 10-13). The aim was to investigate their interaction with DNA and RNA G-quadruplexes, their uptake in malignant and nonmalignant cells, and their capacity to modulate gene expression and inhibit cell growth. Flow cytometry showed that the ATPDs enter more efficiently in malignant T24 bladder cells than in nonmalignant embryonic kidney 293 or fibroblast NIH 3T3 cells. In T24 malignant cells, compound 1, with two ethyl side chains, is taken up by endocytosis, while 12 and 13, with respectively propyl and butyl side chains, are transported by passive diffusion. The designed ATPDs localize in the cytoplasm and nucleus and tightly bind to DNA and RNA G-quadruplexes. They also decrease HRAS expression, increase the cell population in G_0/G_1, and strongly inhibit proliferation in malignant T24 bladder cells, but not in nonmalignant 293 or NIH 3T3 cells.
机译:我们制备了一系列具有不同长度的胍基-烷基侧链的蒽噻吩二酮(ATPD)(化合物1、10-13)。目的是研究它们与DNA和RNA G四联体的相互作用,在恶性和非恶性细胞中的摄取,以及它们调节基因表达和抑制细胞生长的能力。流式细胞仪显示,在恶性T24膀胱细胞中,ATPD比非恶性胚胎肾293或成纤维细胞NIH 3T3细胞更有效地进入。在T24恶性细胞中,具有两个乙基侧链的化合物1通过内吞作用吸收,而分别具有丙基和丁基侧链的12和13通过被动扩散转运。设计的ATPD位于细胞质和细胞核中,并与DNA和RNA G四联体紧密结合。它们还降低HRAS表达,增加G_0 / G_1中的细胞数量,并强烈抑制恶性T24膀胱细胞的增殖,但不能抑制非恶性293或NIH 3T3细胞的增殖。

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