Induced apoptosis and necrosis by 2-methylfuranonaphthoquinone in human cervical cancer HeLa cells.

Cancer detection and prevention Pub Date : 2000-01-01
J Pan, E Simamura, J Koyama, H Shimada, K I Hirai
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Abstract

2-Methylnaphtho[2,3-b]furan-4,9-dione (FNQ3) has been reported to be more cytotoxic to human malignant tumor cell lines than are the corresponding normal epithelial cells. Therefore, we examined the dose response of FNQ3 against human cervical cancer HeLa cells in culture. When 1.25 mg/ml FNQ3 was applied, apoptosis was induced, as determined by an immunohistochemical staining of fragmented genome DNA and cell profiles. Significant inhibition of Bcl-2 oncogene protein expression by the same concentration of FNQ3 also was demonstrated by an immunohistochemical staining method to visualize the expressed cells and Western blot in polyacrylamide gel electrophoresis. Flow-cytometric spectra showed S-phase arrest in cell cycles and the appearance of sub-G1 phase consistent with apoptosis. On the other hand, concentrations of 5 microg/ml or more of FNQ3 induced necrosis. These results show that FNQ3 may act as an antitumor agent to induce apoptosis by affecting Bcl-2 expression and cell cycles, or necrosis as the result of primary mitochondrial injuries.

2-甲基呋喃醌诱导人宫颈癌HeLa细胞凋亡和坏死。
据报道,2-甲基萘[2,3-b]呋喃-4,9-二酮(FNQ3)对人类恶性肿瘤细胞系的细胞毒性高于相应的正常上皮细胞。因此,我们检测了FNQ3对培养的人宫颈癌HeLa细胞的剂量反应。当1.25 mg/ml FNQ3加入时,通过片段基因组DNA和细胞谱的免疫组化染色确定细胞凋亡。同样浓度的FNQ3对Bcl-2癌基因蛋白的表达也有明显的抑制作用,免疫组织化学染色法显示了表达的细胞和聚丙烯酰胺凝胶电泳的Western blot。流式细胞术显示细胞周期的s期阻滞和亚g1期的出现与凋亡一致。另一方面,浓度在5微克/毫升以上的FNQ3诱导坏死。这些结果表明,FNQ3可能通过影响Bcl-2的表达和细胞周期,或影响线粒体原发损伤导致的细胞坏死,从而作为抗肿瘤药物诱导细胞凋亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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