Embelin与他莫昔芬和多西他赛对人乳腺癌MCF-7和MDA MB-231细胞增殖的细胞毒作用比较

G. Abusoglu, C. Kocak, F. E. Kocak, B. Öztürk, H. Vatansev
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引用次数: 0

摘要

检测促凋亡Bax和抗凋亡Bcl-2染色的途径。Bax表达量升高(p<0.05), Bcl-2表达量降低(p<0.05)。结论:总的来说,Embelin对两种乳腺癌细胞类型的癌细胞增殖均有抑制作用,其作用程度取决于剂量和时间。我们发现,与他莫昔芬和多西他赛相比,Embelin在分子水平上更有效,特别是在激素受体阴性的MDA MB-231细胞中。结论认为,特别是在激素受体阴性的乳腺癌中,Embelin更有效,可能成为未来乳腺癌治疗的一种新的替代抗肿瘤药物。本研究结果可为今后的体内研究提供指导。
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Comparison of the cytotoxic effect of Embelin with tamoxifen and docetaxel on human breast cancer MCF-7 and MDA MB-231 cell proliferation
pathways, preparations stained with proapoptotic Bax and antiapoptotic Bcl-2 were examined. Accordingly, while Bax expression level increased (p<0.05), Bcl-2 expression level decreased (p<0.05). Conclusion: In general, Embelin inhibits cancer cell proliferation in both breast cancer cell types, depending on dose and time. We found that Embelin was statistically more effective at the molecular level when compared to both Tamoxifen and Docetaxel, especially in hormone receptor-negative MDA MB-231 cells. By concluding that it is more effective especially in hormone receptor-negative breast cancer, Embelin may be an alternative new antitumoral agent in the treatment of breast cancer in the future. The results of this study may guide for in vivo studies in future.
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0.50
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17
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