Formelli F, Ronchi E, Di Fronzo G
Anticancer Res. 1985 May-Jun;5(3):313-9.
The effect of high and low doses of medroxyprogesterone acetate (MPA) was investigated on three transplanted murine tumors (MXT mammary carcinoma, colon 38, and colon 26) in relation to receptor status and sensitivity of the tumors to ovariectomy and treatment with dexamethasone. MPA had no inhibitory activity on the growth of these tumors. It had no effect on the ovarian-sensitive MXT tumor; it significantly enhanced the growth of an MXT tumor line, selected through serial transplantations, which was stimulated also in ovariectomized animals. MPA, as well as ovariectomy, stimulated the growth of the colon 38 tumor, but this hormone sensitivity was lost during serial transplantations. No correlation was found between the effects of MPA and ovariectomy and the steroid receptor status of these tumors. MPA effects on these tumors do not seem contingent upon a glucocorticoid-like action since dexamethasone was highly effective on all the tested tumors. The combined treatment of the colon 26 tumor with a cytotoxic drug, 4'-deoxydoxorubicin, and MPA, which administered alone stimulated tumor growth and increased life span, caused a slight increase in the life span compared to single agents alone.
研究了高剂量和低剂量醋酸甲羟孕酮(MPA)对三种移植性小鼠肿瘤(MXT乳腺癌、结肠38癌和结肠26癌)的影响,这些影响与肿瘤的受体状态以及肿瘤对卵巢切除术和地塞米松治疗的敏感性有关。MPA对这些肿瘤的生长没有抑制活性。它对卵巢敏感的MXT肿瘤没有影响;它显著促进了通过连续传代选择的MXT肿瘤细胞系的生长,这种细胞系在去卵巢动物中也受到刺激。MPA以及卵巢切除术均刺激了结肠38肿瘤的生长,但在连续传代过程中这种激素敏感性丧失了。未发现MPA和卵巢切除术的作用与这些肿瘤的类固醇受体状态之间存在相关性。MPA对这些肿瘤的作用似乎并非取决于糖皮质激素样作用,因为地塞米松对所有测试肿瘤都非常有效。结肠26肿瘤与细胞毒性药物4'-脱氧阿霉素和MPA联合治疗,单独使用MPA会刺激肿瘤生长并延长生存期,与单独使用单一药物相比,联合治疗使生存期略有增加。