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两性霉素B1增强抗癌药对敏感和耐药AKR白血病的细胞毒性。

Potentiation of anticancer agent cytotoxicity against sensitive and resistant AKR leukemia by amphotericin B1.

作者信息

Valeriote F, Medoff G, Dieckman J

出版信息

Cancer Res. 1979 Jun;39(6 Pt 1):2041-5.

PMID:445402
Abstract

Amphotericin B was able to enhance the effects of actinomycin D (Act-D), adriamycin, and vincristine against AKR leukemia. AKR leukemia lines of increasing resistance to Act-D were obtained by passage in syngeneic mice treated with Act-D. The cells selected for Act-D resistance also eventually became cross-resistant to vincristine and Adriamycin, but resistance to these agents developed at a slower rate. Amphotericin B enhanced the effects of all these agents against the resistant cells, although the degree of enhancement varied among these antitumor agents and decreased as drug resistance increased in the late-passage leukemia lines.

摘要

两性霉素B能够增强放线菌素D(Act-D)、阿霉素和长春新碱对AKR白血病的疗效。通过在接受Act-D治疗的同基因小鼠体内传代,获得了对Act-D耐药性不断增加的AKR白血病细胞系。选择出的对Act-D耐药的细胞最终也对长春新碱和阿霉素产生了交叉耐药性,但对这些药物的耐药性发展速度较慢。两性霉素B增强了所有这些药物对耐药细胞的疗效,尽管增强程度在这些抗肿瘤药物中有所不同,并且随着传代后期白血病细胞系耐药性的增加而降低。

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