Buommino E, Nicoletti R, Gaeta G M, Orlando M, Ciavatta M L, Baroni A, Tufano M A
Department of Experimental Medicine, Section of Microbiology and Clinical Microbiology, Second University of Naples, Italy.
Cell Prolif. 2004 Dec;37(6):413-26. doi: 10.1111/j.1365-2184.2004.00323.x.
3-O-Methylfunicone (OMF) is a secondary metabolite produced by the soil fungus Penicillium pinophilum which has cytostatic properties. The aim of this study was to investigate the mechanisms by which such properties are exerted, with special reference to any anti-proliferative and apoptotic potential, on HeLa cells. OMF treatment caused about 44% inhibition of cell growth after 24 h, and modifications in the tubulin fibre organization. In addition, a significant increase in p21 mRNA expression and a decrease in cyclin D1 and Cdk4 mRNA expression resulted at the same time. Apoptosis induction was demonstrated by the annexin V assay, cytofluorimetric analysis of the DNA content of the sub-G1 fraction and DNA laddering. Taken together, our data showed that the compound inhibits proliferation of HeLa cells by several mechanisms, such as disruption of tubulin fibres, cell cycle arrest and apoptosis induction. The capacity of the compound to affect the cell cycle and to modulate apoptosis is indicative of a potential for the development of a new agent for cancer chemotherapy.
3 - O - 甲基富尼酮(OMF)是土壤真菌嗜松青霉产生的一种具有细胞生长抑制特性的次生代谢产物。本研究的目的是探讨该物质发挥这些特性的机制,特别关注其对人宫颈癌HeLa细胞的抗增殖和凋亡潜力。OMF处理24小时后导致细胞生长抑制约44%,并使微管蛋白纤维组织发生改变。此外,同时p21 mRNA表达显著增加,细胞周期蛋白D1和细胞周期蛋白依赖性激酶4(Cdk4)mRNA表达降低。膜联蛋白V检测、亚G1期细胞DNA含量的细胞荧光分析和DNA梯状条带分析均证实了凋亡的诱导。综上所述,我们的数据表明该化合物通过多种机制抑制HeLa细胞增殖,如破坏微管蛋白纤维、细胞周期阻滞和诱导凋亡。该化合物影响细胞周期和调节凋亡的能力表明其具有开发新型癌症化疗药物的潜力。