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福莫司汀、达卡巴嗪与质子照射单一及联合治疗后人类黑色素瘤细胞的活力

Viability of a human melanoma cell after single and combined treatment with fotemustine, dacarbazine, and proton irradiation.

作者信息

Petrović Ivan M, Korićanac Lela B, Todorović Danijela V, Ristić-Fira Aleksandra M, Valastro Lucia M, Privitera Giuseppe, Cuttone Giacomo

机构信息

Vinca Institute of Nuclear Sciences, Laboratory for Molecular Biology and Endocrinology, P.O. Box 522, 11001 Belgrade, Serbia.

出版信息

Ann N Y Acad Sci. 2007 Jan;1095:154-64. doi: 10.1196/annals.1397.019.

Abstract

Viability of human HTB140 melanoma cells after being exposed to fotemustine (FM) and dacarbazine (DTIC) as well as to proton irradiation was studied. Effects of 100 and 250 microM drugs were assessed after incubation of 6, 24, 48, 72, and 96 h. Irradiations were performed with 62 MeV therapeutic protons, delivering to the cell monolayer single doses of 2, 4, 8, 12, and 16 Gy. Viability was evaluated 7 days after irradiation. Inactivation level was estimated using microtetrasolium (MTT) and sulforhodamine B (SRB) assays. Combined effects of each drug and protons, were carried out using the same drug concentrations. Proton doses applied were those used in therapy, that is, 12 and 16 Gy. With the increase of drug concentration or irradiation dose, level of cell inactivation reached approximately 60%, 48 h after drug treatment or 7 days after irradiation at 16 Gy. Considering the rate of drug concentrations used, as well as the level of doses applied, it appears that HTB140 cells are more resistant to proton irradiation than to alkylating agents tested. The combined treatment with FM or DTIC and protons did not show significant changes of cell viability as compared to the effects of single agents. Since the time point for measuring cumulative effects of drug and irradiation was 48 h post irradiation, it seems that the obtained level of viability could be attributed primarily to the effects of drugs.

摘要

研究了人HTB140黑色素瘤细胞在暴露于福莫司汀(FM)、达卡巴嗪(DTIC)以及质子照射后的活力。在6、24、48、72和96小时孵育后,评估了100和250微摩尔药物的作用。使用62兆电子伏特治疗性质子进行照射,向细胞单层递送2、4、8、12和16戈瑞的单剂量。在照射7天后评估活力。使用微量四氮唑蓝(MTT)和磺酰罗丹明B(SRB)测定法估计失活水平。每种药物与质子的联合作用,使用相同的药物浓度进行。应用的质子剂量是治疗中使用的剂量,即12和16戈瑞。随着药物浓度或照射剂量的增加,在药物处理48小时后或16戈瑞照射7天后,细胞失活水平达到约60%。考虑到所使用的药物浓度速率以及应用的剂量水平,似乎HTB140细胞对质子照射的抗性比对所测试的烷基化剂更强。与单一药物的作用相比,FM或DTIC与质子的联合治疗未显示细胞活力有显著变化。由于测量药物和照射累积效应的时间点是照射后48小时,似乎所获得的活力水平可能主要归因于药物的作用。

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