ß-榄香烯增强A375人黑色素瘤细胞的放射致敏性

Zahra Balavandi, A. Neshasteh-Riz, Fereshteh Koosha, Samira Eynali, M. Hoormand, M. Shahidi
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引用次数: 13

摘要

黑色素瘤是恶性程度最高、最严重的一种皮肤癌。它是一种转移风险高且对传统治疗方法(手术、放疗和化疗)有耐药性的肿瘤。β-榄香烯是姜黄文玉金中最有效的成分,是一种非细胞毒性的抗肿瘤药物,对不同类型的癌症均有疗效。本研究旨在探讨β-榄香烯联合放疗对A375人黑色素瘤的治疗效果。材料与方法本实验采用单层培养法培养人黑色素瘤细胞。处理过程是通过向细胞中添加不同浓度的β-榄香烯来完成的。然后,在不同的孵育时间(24、48和72小时)将细胞暴露于2和4 Gy x射线下。MTT法测定细胞活力。采用Annexin V/PI法研究细胞凋亡反应率。结果MTT实验结果显示,β-榄香烯对辐照细胞增殖具有剂量依赖性和时间依赖性。流式细胞术分析表明β-榄香烯具有诱导细胞凋亡的作用。此外,放射联合治疗显著降低了细胞的增殖能力,并促进了细胞凋亡。例如,暴露于40µg/ml β-榄香烯组的细胞存活率为80%,但在2 Gy剂量下的6 MV X射线联合处理将细胞存活率降低至61%。结论β-榄香烯通过凋亡抑制人黑色素瘤癌细胞的增殖。结果表明,β-榄香烯能显著提高A375细胞株的放射敏感性。本研究结果表明β-榄香烯治疗黑色素瘤细胞的有效性,以及在该领域进一步研究的必要性。
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The Use of ß-Elemene to Enhance Radio Sensitization of A375 Human Melanoma Cells
Objective Melanoma is the most malignant and severe type of skin cancer. It is a tumor with a high risk of metastasis and resistant to conventional treatment methods (surgery, radiotherapy, and chemotherapy). β-elemene is the most active constituent of Curcuma wenyujin which is a non-cytotoxic antitumor drug, proved to be effective in different types of cancers. The study aimed to investigate the therapeutic effects of β-elemene in combination with radiotherapy on A375 human melanoma. Materials and Methods In this experimental study, human melanoma cells were grown in the monolayer culture model. The procedure of the treatment was performed by the addition of different concentrations of β-elemene to the cells. Then, the cells were exposed to 2 and 4 Gy X-ray in different incubation times (24, 48, and 72 hours). The MTT assay was used for the determination of the cell viability. To study the rate of apoptosis response to treatments, the Annexin V/PI assay was carried out. Results The results of the MTT assay showed β-elemene reduced the cell proliferation in dose- and time-dependent manners in cells exposed to radiation. Flow cytometry analysis indicated that β-elemene was effective in the induction of apoptosis. Furthermore, the combination treatment with radiation remarkably decreased the cells proliferation ability and also enhanced apoptosis. For example, cell viability in a group exposed to 40 µg/ml of β-elemene was 80%, but combination treatment with 6 MV X beam at a dose of 2 Gy reduced the viability to 61%. Conclusion Our results showed that β-elemene reduced the proliferation of human melanoma cancer cell through apoptosis. Also, the results demonstrated that the radio sensitivity of A375 cell line was significantly enhanced by β-elemene. The findings of this study indicated the efficiency of β-elemene in treating melanoma cells and the necessity for further research in this field.
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