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西卡前列素不影响细胞毒性药物的肿瘤抑制潜力。

Cicaprost does not affect tumor inhibitory potential of cytostatic drugs.

作者信息

Schirner M, Schneider M

机构信息

Schering AG Berlin, Experimental Oncology, Federal Republic of Germany.

出版信息

Anticancer Res. 1993 May-Jun;13(3):743-6.

PMID:8317906
Abstract

Cicaprost, a stable prostacyclin analogue with antimetastatic potential, was investigated as regards its effect on the tumor inhibitory potential of cytostatic drugs exhibiting different modes of action in the MXT-OVEX mouse mammary carcinoma. Cicaprost itself in doses of 0.5 mg/Kg and 1.0 mg/Kg po. daily had no effect on the growth of the sc.-implanted tumor. cis-Platinum at a dose of 1.5 mg/Kg sc. strongly inhibited tumor growth, while at a dose of 0.75 mg/Kg only a weak effect was seen. The efficacy of both treatments was not altered by cicaprost (0.5 mg/Kg; po.) administered in two different schedules. Whereas cyclophosphamide (400 mg/Kg; sc) completely inhibited the growth of the MXT-OVEX tumor, doxorubicin (2.5 mg/kg; sc.) and 5-FU (10 mg/Kg; sc.) had only a weak effect. The combination of cicaprost with either cyclophosphamide, doxorubicin or 5-FU did not alter the inhibition of tumor growth. On the basis of these data, we anticipate that the antimetastatic agent cicaprost can be used in combination with cytostatic regimens without interfering with their clinical effectiveness.

摘要

西卡前列素是一种具有抗转移潜力的稳定前列环素类似物,针对其对在MXT-OVEX小鼠乳腺癌中表现出不同作用模式的细胞毒性药物的肿瘤抑制潜力的影响进行了研究。西卡前列素以0.5毫克/千克和1.0毫克/千克的口服剂量每日给药,对皮下植入肿瘤的生长没有影响。顺铂以1.5毫克/千克的皮下剂量强烈抑制肿瘤生长,而以0.75毫克/千克的剂量仅观察到微弱效果。两种治疗方案的疗效均未因以两种不同给药方案给予西卡前列素(0.5毫克/千克;口服)而改变。环磷酰胺(400毫克/千克;皮下)完全抑制了MXT-OVEX肿瘤的生长,而阿霉素(2.5毫克/千克;皮下)和5-氟尿嘧啶(10毫克/千克;皮下)仅产生微弱效果。西卡前列素与环磷酰胺、阿霉素或5-氟尿嘧啶联合使用均未改变对肿瘤生长的抑制作用。基于这些数据,我们预计抗转移药物西卡前列素可与细胞毒性治疗方案联合使用,而不干扰其临床疗效。

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