【同时联合化疗的考虑——Dunn骨肉瘤和NR纤维肉瘤采用试管内接触肿瘤细胞悬液和皮下接种的敏感性试验】。

Nihon Gan Chiryo Gakkai shi Pub Date : 1990-12-20
O Inoue, K Ibaraki, H Shimabukuro, Y Shingaki
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引用次数: 0

摘要

从恶性肿瘤的化疗敏感性试验来看,多药联合化疗的基本概念还没有得到很好的认识。为了研究Dunn骨肉瘤和NR纤维肉瘤两种抗癌药物之间的同时相互作用,我们建立了体外生物测定的化疗敏感性试验。将任一小鼠肉瘤细胞悬浮液0.1 ml浸入含有丝裂霉素(MC)、环磷酰胺(CPM)、长春新碱(VC)、博来霉素(BM)、5-FU、阿霉素(ADM)、顺铂(CDDP)或甲氨蝶呤(MTX)等抗癌剂的0.4 ml RPMI 1640细胞培养液中,在37℃下孵育3或6小时。然后将沉淀的细胞悬液0.1 ml接种于C3H小鼠背部皮下,提供4个部位进行4种不同的敏感性试验。在3周内,如果肿瘤未见生长,则评估药物的敏感性为阳性,如果肿瘤直径大于10 mm,则评估药物的敏感性为阴性。然后,用相同的方法对每只小鼠肉瘤进行8种抗癌药物中2种药物联合的抗肿瘤作用测定。在Dunn骨肉瘤或NR纤维肉瘤中,2种敏感性阳性药物联合使用未发现明显的协同作用。除与CPM联用具有较强的抗肿瘤作用外,任何一种敏感性阳性药物与另一种敏感性阴性药物联用,其抗肿瘤作用均明显降低。2种敏感性阴性药物联合使用未产生任何抗肿瘤作用。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Consideration of simultaneous combination chemotherapy--employing a sensitivity test in Dunn osteosarcoma and NR fibrosarcoma by intra-test tube contact of tumor cell suspension, and subcutaneous inoculation].

Fundamental concepts of combination multi-drug chemotherapy have not been well recognized from the aspects of chemo-sensitivity test upon malignant tumors. A chemo-sensitivity test by in-vitro bioassay for Dunn osteosarcoma and NR fibrosarcoma was developed by us to study the simultaneous interactions between two anticancerous agents. 0.1 ml of cell suspension of either mouse sarcoma was immersed in 0.4 ml of RPMI 1640 cell culture medium containing an anticancerous agent such as Mitomycin (MC), Cyclophosphamide (CPM), Vincristine (VC), Bleomycin (BM), 5-FU, Adriamycin (ADM), Cisplatin (CDDP) or Methotrexate (MTX) in a test-tube, and incubated at 37 degrees C for 3 or 6 hours. Then, the sedimented cell suspension of 0.1 ml was inoculated subcutaneously in the dorsum of C3H mouse which provided 4 sites for 4 different sensitivity tests. In 3 weeks, sensitivities of the anticancerous agents were evaluated as positive sensitivity if no growth of the tumor was observed, or negative sensitivity if the growth of more than 10 mm in diameter was observed. Then, the determination of antitumorous effect on 2-drug combination out of the 8 anticancerous agents, were performed on each mouse sarcoma by the same method. In Dunn osteosarcoma or NR fibrosarcoma, the combination of 2 sensitivity-positive agents revealed no apparent synergistic effects. In any combinations of one sensitivity-positive agent with the other sensitivity-negative agent, except the combinations with CPM which possessed mighty antitumorous effect, apparent reduction of antitumorous effects was observed. The combination of 2 sensitivity-negative agents never produced any antitumorous effects.(ABSTRACT TRUNCATED AT 250 WORDS)

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