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来自假单胞菌属M-6-3的多粘菌素酰基转移酶的体外抗肿瘤活性

In vitro antitumor activity of polymyxin acylase from Pseudomonas sp. M-6-3.

作者信息

Yasuda N, Matsunaga H, Kimura Y, Tanaka M, Sasaki T

机构信息

Faculty of Pharmaceutical Sciences, Mukogawa Women's University, Nishinomiya, Japan.

出版信息

Biol Pharm Bull. 1995 Apr;18(4):615-7. doi: 10.1248/bpb.18.615.

Abstract

Polymyxin acylase from Pseudomonas sp. M-6-3 can deacylate not only polymyxin group antibiotics, but also the long-chain fatty acyl group of proteins and peptides. We found the in vitro antitumor activity of polymyxin acylase against murine and human tumor cells, especially KB cells. The mechanism of the antitumor activity remains equivocal, but we speculate that it may result from the affinity of polymyxin acylase for long-chain fatty acyl proteins in human carcinoma cells.

摘要

来自假单胞菌属M-6-3的多粘菌素酰基转移酶不仅可以使多粘菌素类抗生素脱酰基,还能使蛋白质和肽的长链脂肪酰基脱酰基。我们发现多粘菌素酰基转移酶对小鼠和人类肿瘤细胞,尤其是KB细胞具有体外抗肿瘤活性。抗肿瘤活性的机制尚不清楚,但我们推测这可能是由于多粘菌素酰基转移酶对人类癌细胞中长链脂肪酰基蛋白质的亲和力所致。

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