榕树乙酸乙酯部位的增效作用。f、阿霉素化疗对T47D人乳腺癌细胞系的影响。

Agung E Nugroho, Adam Hermawan, P Putri D, Edy Meiyanto, Lukman Hakim
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引用次数: 10

摘要

目的:对竹叶榕醇提物进行研究。f. (Moraceae)叶片及其乙酸乙酯可溶性组分(EASF)对T47D乳腺癌细胞有明显的细胞毒作用。在本研究中,我们进一步研究了败草叶乙醇提取物EASF与阿霉素联合对T47D乳腺癌细胞株的细胞毒性、细胞周期阻滞和诱导凋亡的影响。方法:采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑法对T47D细胞进行细胞毒作用分析。使用流式细胞仪分析细胞周期分布,使用ModFit LT 3.0程序分析数据。采用溴化乙啶-吖啶橙双染色法进行细胞凋亡试验。采用免疫组织化学技术检测了裂解型聚adp核糖聚合酶在T47D细胞系中的表达。结果:阿霉素(2 ~ 8 nmol/L)与EASF (0.875 ~ 7 μg/mL)联合对T47D细胞生长的抑制作用强于阿霉素单药。此外,阿霉素与EASF联用可增加细胞凋亡发生率。发现EASF通过改变细胞周期G(2)/M至G(1)期的抑制作用,提高阿霉素的细胞毒作用。与单独处理相比,联合处理对T47D细胞中cleaved-PARP表达的刺激作用更强。结论:EASF可能通过诱导T47D细胞凋亡和细胞周期阻滞来增强阿霉素在T47D细胞中的活性。
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Synergistic effects of ethyl acetate fraction of Ficus septica Burm. f. and doxorubicin chemotherapy on T47D human breast cancer cell line.

Objective: Previously, ethanolic extract of Ficus septica Burm. f. (Moraceae) leaves and its ethyl acetate soluble fraction (EASF) exhibited potent cytotoxic effects on T47D breast cancer cells. In the present study, we further investigated the effects of EASF of ethanolic extract of F. septica leaves in combination with doxorubicin on T47D breast cancer cell line in cytotoxicity, cell cycle arrest and apoptosis induction.

Methods: The cytotoxic effect analysis on T47D cells was carried out using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Analysis of cell cycle distribution was performed using a flowcytometer and the data were analyzed using ModFit LT 3.0 program. Apoptosis assay was carried out by double staining method using ethidium bromide-acridin orange. The expression of cleaved-poly ADP-ribose polymerase in the T47D cell line was identified using immunohistochemical techniques.

Results: The combination of doxorubicin (2 to 8 nmol/L) with EASF (0.875 to 7 μg/mL) more potently inhibited cell growth than the single treatment of doxorubicin in T47D cells. In addition, the combination of doxorubicin and EASF could increase the incidence of cells undergoing apoptosis. EASF was found to improve cytotoxic effect of doxorubicin by changing the inhibition of cell cycle G(2)/M to G(1) phase. The combination also exhibited a more intensive stimulatory effect on cleaved-PARP expression in T47D cells than the single treatment.

Conclusion: It is concluded that EASF may enhance doxorubicin activities in T47D cells by inducing apoptosis and cell cycle arrest.

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