Faculty of Medicine, University of Medicine and Pharmacy of Craiova , Craiova, Romania.
Faculty of Pharmacy, Pharmaceutical Technology Department, University of Medicine and Pharmacy of Craiova , Craiova, Romania.
J Immunoassay Immunochem. 2020 Nov 1;41(6):1033-1043. doi: 10.1080/15321819.2020.1819309. Epub 2020 Oct 6.
Prior to 2000, the DNA alkylating agents nitrosoureas were used as standard treatment of glioblastoma. Current treatments for glioblastoma patients consist of surgery followed by radiation in combination with temozolomide. Despite therapeutic advances, the prognosis for glioblastoma patients remains grim, with a five-year overall survival below 15%. In this study, our team analyzed the interaction between temozolomide and doxorubicin in a glioblastoma cell line, .
The cell line, established from a patient who underwent surgery at the "Bagdasar Arseni Emergency Hospital", was exposed to 10 µM and 100 µM of temozolomide and 10 nM and 100 nM of doxorubicin, respectively, over a period of 7, 10 and 14 days, in monotherapy and in combination.
The results showed that both temozolomide (66.5% cytotoxicity for the 10 µM dose at 14 days) de and doxorubicin (66.8% cytotoxicity for the 10 nM dose after 14 days) were very effective in killing cancer cells in monotherapy, but failed to produce a synergistic effect when used in combination.
While the results may be discouraging, they present an interesting prospect into how certain drug interactions can impact treatment response.
在 2000 年之前,DNA 烷化剂亚硝脲类药物被用作胶质母细胞瘤的标准治疗方法。目前胶质母细胞瘤患者的治疗方法包括手术,随后进行放疗联合替莫唑胺治疗。尽管治疗取得了进展,但胶质母细胞瘤患者的预后仍然严峻,五年总生存率低于 15%。在这项研究中,我们的团队分析了替莫唑胺和阿霉素在胶质母细胞瘤细胞系中的相互作用。
该细胞系是从在“Bagdasar Arseni 急诊医院”接受手术的患者中建立的,分别用 10µM 和 100µM 的替莫唑胺以及 10nM 和 100nM 的阿霉素处理,持续 7、10 和 14 天,分别进行单药治疗和联合治疗。
结果表明,替莫唑胺(14 天 10µM 剂量时的细胞毒性为 66.5%)和阿霉素(14 天 10nM 剂量时的细胞毒性为 66.8%)在单药治疗中均能非常有效地杀死癌细胞,但联合使用时未能产生协同作用。
虽然结果可能令人沮丧,但它们提供了一个有趣的前景,即某些药物相互作用如何影响治疗反应。