D'Alessandro N, Borsellino N
Instituto de Farmacologia, Facoltá di Medicina e Chirurgia dell'Universitá di Palermo, Italy.
Anticancer Drugs. 1996 May;7(3):281-7. doi: 10.1097/00001813-199605000-00007.
Having observed that tumor necrosis factor (TNF)-alpha and doxorubicin (DXR) produce a synergistic inhibition of melanoma B16 and also of its multidrug resistant (MDR) variant in vitro, we tested whether this interaction would occur in vivo as well. C57BL/6 mice with s.c. tumors were treated with TNF or flavone acetic acid (FAA), a biological response modifier, in simultaneous or sequential combination with DXR. The agents were administered systemically. Overall, the results were negative, apart from a trend towards slight synergy, found in the chemosensitive melanoma, when TNF was given 1 or 2 days before DXR. The effects of FAA and DXR were found to be subadditive or antagonistic. However, an encouraging new finding was that FAA has significant inhibitory effects on the MDR B16 melanoma.
在观察到肿瘤坏死因子(TNF)-α和阿霉素(DXR)在体外对黑色素瘤B16及其多药耐药(MDR)变体产生协同抑制作用后,我们测试了这种相互作用在体内是否也会发生。对皮下接种肿瘤的C57BL/6小鼠,用TNF或生物反应调节剂黄酮乙酸(FAA)与DXR同时或序贯联合给药。这些药物通过全身给药。总体而言,结果为阴性,不过在对化疗敏感的黑色素瘤中,当在DXR前1或2天给予TNF时,发现有轻微协同作用的趋势。FAA和DXR的作用被发现是相加不足或拮抗的。然而,一个令人鼓舞的新发现是,FAA对MDR B16黑色素瘤有显著抑制作用。