Talebpoor Maryam, Neshasteh-Riz Ali, Koosha Fereshteh, Eynali Samira
MSc, Radiation Biology Research Center, Iran University of Medical Sciences, Tehran, Iran.
MSc, Department of Radiation Sciences, School of Paramedicine, Iran University of Medical Sciences, Tehran, Iran.
J Biomed Phys Eng. 2022 Jun 1;12(3):267-276. doi: 10.31661/jbpe.v0i0.1912-1000. eCollection 2022 Jun.
Melanoma is categorized as one of the most malignant, severe, and lethal cancers of the skin. Regarding the lack of efficiency of conventional therapies for most patients, novel therapeutic strategies are strongly required.
The current study aimed to assess the impact of AZD6738- an ATR kinase inhibitor- in combination with 6 MV X-ray on the human melanoma cell line (A375).
In this experimental study, cells were treated with different concentrations of AZD6738 for 24 and 48 h in the presence and absence of radiation (2 Gy, 4 Gy, and 6 Gy). The cell viability and cell proliferation assay were examined in both experimental and control groups by MTT and colony formation techniques, respectively.
The results indicated that by increasing the concentration of AZD6738, the cell viability was markedly diminished in all treatment groups. As expected, the cell viability of the cells treated with AZD6738 and radiation was significantly lower than the group treated with AZD6738 alone. Besides, the combinatory treatment significantly decreased cell proliferation in the melanoma cell line. The combination of AZD6738 with radiation resulted in a significant increase in cytotoxicity by a 50% increase in cell death when used at concentrations of 0.3 µM, 1 µM, 1.51 µM, and 1.61 µM, respectively.
The combination of AZD6738 with radiation possesses a synergistic effect on the reduction of the cell viability and proliferation of melanoma cells. This present study provides insight into the impact of Ataxia Telangiectasia and Rad3-related kinase (ATR) inhibition on the potential role of this kinase in the suppression of melanoma cell proliferation.
黑色素瘤被归类为皮肤最恶性、最严重和最致命的癌症之一。鉴于大多数患者的传统治疗方法缺乏疗效,强烈需要新的治疗策略。
本研究旨在评估 ATR 激酶抑制剂 AZD6738 与 6 MV X 射线联合对人黑色素瘤细胞系(A375)的影响。
在本实验研究中,在有和无辐射(2 Gy、4 Gy 和 6 Gy)的情况下,用不同浓度的 AZD6738 处理细胞 24 小时和 48 小时。分别通过 MTT 和集落形成技术在实验组和对照组中检测细胞活力和细胞增殖测定。
结果表明,随着 AZD6738 浓度的增加,所有治疗组的细胞活力均显著降低。正如预期的那样,用 AZD6738 和辐射处理的细胞的细胞活力明显低于单独用 AZD6738 处理的组。此外,联合治疗显著降低了黑色素瘤细胞系中的细胞增殖。当分别以浓度 0.3 μM、1 μM、1.51 μM 和 1.61 μM 使用时,AZD6738 与辐射的组合导致细胞毒性显著增加,细胞死亡增加 50%。
AZD6738 与辐射的组合对降低黑色素瘤细胞的活力和增殖具有协同作用。本研究深入了解了共济失调毛细血管扩张症和 Rad3 相关激酶(ATR)抑制对该激酶在抑制黑色素瘤细胞增殖中的潜在作用的影响。