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A Novel Carbazole Derivative,BMVC:a Potential Antitumor Agent and Fluorescence Marker of Cancer Cells

机译:新型咔唑衍生物BMVC:一种潜在的抗肿瘤药物和癌细胞的荧光标记

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摘要

We have investigated a novel compound,3,6-bis[2-(l-methylpyridinium)vinyl]carbazole diiodide (BMVC),for inhibiting telomerase activity and distinguishing human lung H1299 and oral Ca9-22 cancer cells from lung IMR90 and skin Detroit-551 normal fibroblast cells.The telomeric repeat amplification protocol (TRAP) assay shows that the concentration of BMVC that inhibits 50% of the telomerase activity (IC_(50)) is ca.0.05 muM.On the other hand,the cell-viability assay indicates that the cytotoxicity was less than 15% to the H1299 and Ca9-22 cancer cells,and almost negligible to the MRC-5 and Detroit-551 normal cells after incubation with 0.5 UM BMVC for 72 h.The low concentration of 0.05 UM of BMVC can inhibit telomerase activity but does not have general toxic effects to normal cells,implying that BMVC is a promising telomerase inhibitor.Moreover,wide-field fluorescence images of 0.1 UM BMVC-treated cells show bright fluorescence spots in the nuclei of the most H1299 and Ca9-22 cancer cells.Interestingly,similar fluorescence spots are hardly observed in the nuclei of the IMR90 and Detroit-551 normal cells,implying that BMVC might be a useful marker to distinguish tumor cells and normal cells.
机译:我们研究了一种新型化合物3,6-双[2-(1-(甲基吡啶鎓)乙烯基]咔唑二碘化物(BMVC),用于抑制端粒酶活性并区分人肺H1299和口腔Ca9-22癌细胞与肺IMR90和皮肤底特律-551正常成纤维细胞。端粒重复扩增方案(TRAP)分析表明,抑制50%端粒酶活性(IC_(50))的BMVC浓度约为0.05μM。另一方面,细胞活力检测表明,在0.5 UM BMVC中孵育72 h后,对H1299和Ca9-22癌细胞的细胞毒性小于15%,对MRC-5和Detroit-551正常细胞几乎可以忽略不计。低浓度0.05 UM BMVC可以抑制端粒酶活性,但对正常细胞没有一般的毒性作用,这表明BMVC是一种有前途的端粒酶抑制剂。此外,0.1 UM BMVC处理的细胞的宽视野荧光图像在大多数细胞的核中均显示出明亮的荧光点。 H1299和Ca9-22癌细胞有趣的是,在IMR90和底特律551正常细胞的核中几乎没有观察到相似的荧光斑点,这表明BMVC可能是区分肿瘤细胞和正常细胞的有用标记。

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