Russo P, Parodi S, Billi G, Oliva C, Venturini M, Noviello E, Conte P
Department of Chemical Carcinogenesis, Istituto Nazionale per 1a Ricerca sul Cancro, Genova, Italy.
Jpn J Cancer Res. 1992 Jul;83(7):684-7. doi: 10.1111/j.1349-7006.1992.tb01966.x.
The cytotoxic activity of human recombinant tumor necrosis factor (rHuTNF) (from 0.01 to 10000 U/ml) was assayed on six human ovarian cancer cell lines and one human cervical carcinoma cell line using a crystal violet assay. rHuTNF was cytotoxic to four cell lines (A2780, A2774, SW626, PA1), while 3 cell lines (IGROV1, SKOV3, Me180) were marginally sensitive to its activity. However, under the same experimental conditions rHuTNF markedly enhanced the cytotoxicity of mitoxantrone, a chemotherapeutic drug targeted at DNA topoisomerase II, in six cell lines. The potentiation of mitoxantrone cytotoxicity was not caused by increased drug accumulation after rHuTNF treatment. No significant increase in cytotoxicity to Me180 cell line was seen when rHuTNF was added to mitoxantrone.
使用结晶紫测定法,检测了人重组肿瘤坏死因子(rHuTNF)(浓度范围为0.01至10000 U/ml)对六种人卵巢癌细胞系和一种人宫颈癌细胞系的细胞毒性活性。rHuTNF对四种细胞系(A2780、A2774、SW626、PA1)具有细胞毒性,而三种细胞系(IGROV1、SKOV3、Me180)对其活性敏感性较低。然而,在相同实验条件下,rHuTNF显著增强了米托蒽醌(一种靶向DNA拓扑异构酶II的化疗药物)在六种细胞系中的细胞毒性。rHuTNF处理后米托蒽醌细胞毒性的增强并非由药物积累增加所致。当将rHuTNF添加到米托蒽醌中时,对Me180细胞系的细胞毒性未见显著增加。