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钙调蛋白抑制剂三氟拉嗪增强耐药P388白血病对阿霉素的敏感性

Enhancement of sensitivity to adriamycin in resistant P388 leukemia by the calmodulin inhibitor trifluoperazine.

作者信息

Ganapathi R, Grabowski D

出版信息

Cancer Res. 1983 Aug;43(8):3696-9.

PMID:6861140
Abstract

Resistance to the cytotoxic effects of daunomycin and Adriamycin (ADR) in sublines of Ehrlich ascites and P388 mouse tumors has been demonstrated to be due to reduced cellular accumulation and retention of drug. In this study, the effect of the calmodulin inhibitor trifluoperazine on the cellular accumulation, retention, and cytotoxic effects of ADR in ADR-sensitive (P388/S) and ADR-resistant (P388/R) P388 mouse leukemia cells was determined. In cells treated in suspension culture for 24 hr or for 1 hr followed by plating in soft agar, a noncytotoxic concentration of 4 microM trifluoperazine, enhanced the sensitivity to ADR 2- to 6-fold in P388/R but not in P388/S cells. A marked enhancement in cellular retention rather than accumulation of ADR in only P388/R cells was obtained with trifluoperazine treatment. This study suggests the possible novel use of phenothiazines to improve drug sensitivity of tumors resistant to ADR treatment.

摘要

已证明艾氏腹水癌和P388小鼠肿瘤亚系对柔红霉素和阿霉素(ADR)细胞毒性作用的抗性是由于细胞对药物的摄取和保留减少所致。在本研究中,测定了钙调蛋白抑制剂三氟拉嗪对ADR敏感(P388/S)和ADR抗性(P388/R)P388小鼠白血病细胞中ADR的细胞摄取、保留及细胞毒性作用的影响。在悬浮培养中处理24小时或处理1小时后接种于软琼脂中的细胞中,4 microM三氟拉嗪的无细胞毒性浓度使P388/R细胞对ADR的敏感性提高了2至6倍,但对P388/S细胞无此作用。三氟拉嗪处理仅使P388/R细胞中ADR的细胞保留显著增强,而非摄取增强。本研究提示吩噻嗪类药物可能有新用途,可提高对ADR治疗耐药肿瘤的药物敏感性。

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