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含羞草决明植物酚类物质通过凋亡途径对宫颈癌细胞系的细胞毒性作用。

Cytotoxic effects of Phytophenolics from Caesalpinia mimosoides Lamk on cervical carcinoma cell lines through an apoptotic pathway.

作者信息

Palasap Adisak, Limpaiboon Temduang, Boonsiri Patcharee, Thapphasaraphong Suthasinee, Daduang Sakda, Suwannalert Prasit, Daduang Jureerut

机构信息

Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Medical Sciences, Khon Kaen University, Khon Kaen, Thailand E-mail :

出版信息

Asian Pac J Cancer Prev. 2014;15(1):449-54. doi: 10.7314/apjcp.2014.15.1.449.

Abstract

BACKGROUND

Extracts of Caesalpinia mimosoides Lamk has been reported to possess anticancer effects, but the active ingredients and the anti-cancer mechanisms are still unknown.

MATERIALS AND METHODS

The effects of a C mimosoides Lamk extract on cell proliferation and apoptosis induction in human cervical carcinoma cell lines, namely HeLa, SiHa, and C33A, as well as in normal Vero cells, were investigated.

RESULTS

Treatment with 5 active fractions (F17-F21) of C mimosoides Lamk methanol extracts inhibited cell viability in a dose- and time- dependent manner. Neutral red assays indicated that treatment with F21 significantly decreased the viability of all cervical cancer cell lines compared to F21-treated normal cells. In addition, HPLC analysis revealed that F21 contained multiple phenolic compounds, namely gallic acid, caffeine, vanillic acid, ferulic acid and resveratrol. F21 had the lowest IC50 and, therefore, a much higher cytotoxicity than F20, F17, F19, and F18 by 20-, 25-, 46- and 47- fold, respectively. Analysis of activation of the apoptosis pathway using a caspase 3/7 activity assay revealed that F21 treatment resulted in a considerable increase in caspase activation in all cancer cell lines tested. At the same concentration of F21, HeLa cells had the highest caspase activity (6.5-fold) compared to the control.

CONCLUSION

C mimosoides Lamk may be of value as an alternative therapeutic agent, especially in combination with other compounds offering possible of synergy of action. Moreover, HPV- and non-HPV-related cervical cancer cells may differ in their responses to treatment regimens.

摘要

背景

据报道,含羞草决明提取物具有抗癌作用,但其活性成分和抗癌机制仍不清楚。

材料与方法

研究了含羞草决明提取物对人宫颈癌细胞系(HeLa、SiHa和C33A)以及正常Vero细胞的细胞增殖和凋亡诱导作用。

结果

含羞草决明甲醇提取物的5个活性组分(F17 - F21)处理以剂量和时间依赖性方式抑制细胞活力。中性红试验表明,与F21处理的正常细胞相比,F21处理显著降低了所有宫颈癌细胞系的活力。此外,高效液相色谱分析显示F21含有多种酚类化合物,即没食子酸、咖啡因、香草酸、阿魏酸和白藜芦醇。F21的半数抑制浓度(IC50)最低,因此其细胞毒性分别比F20、F17、F19和F18高20倍、25倍、46倍和47倍。使用半胱天冬酶3/7活性测定法分析凋亡途径的激活情况,结果显示F21处理导致所有测试癌细胞系中的半胱天冬酶激活显著增加。在相同浓度的F21下,与对照组相比,HeLa细胞的半胱天冬酶活性最高(6.5倍)。

结论

含羞草决明可能作为一种替代治疗剂具有价值,特别是与其他可能具有协同作用的化合物联合使用时。此外,人乳头瘤病毒(HPV)相关和非HPV相关的宫颈癌细胞对治疗方案的反应可能不同。

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