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氨基胍对鸟氨酸类似物抑制R3327AT前列腺来源肿瘤体外克隆形成存活的作用的逆转

Aminoguanidine reversal of the inhibitory effects of ornithine analogs on the in vitro clonogenic survival of the R3327AT prostate-derived tumor.

作者信息

Heston W D, Lazan D W, Fair W R

出版信息

Cancer Lett. 1981 Feb;11(4):323-30. doi: 10.1016/0304-3835(81)90098-7.

Abstract

In in vitro studies with the Copenhagen rat prostate-derived tumor cell lines, the activity of ornithine decarboxylase (ODC) of these lines were as sensitive to inhibition by alpha-difluoromethylornithine (alpha-DFMO) as normal prostatic tissue. The in vitro growth of the tumor in calf serum was inhibited by ODC inhibitors alpha-methylornithine and alpha-difluoromethylornithine. This inhibition was partially reversed by the diamine oxidase inhibitor aminoguanidine. Further, alpha-DFMO was not inhibitory to the growth of these cells in sera which lacked diamine oxidase activity, but was inhibitory when diamine oxidase was added.

摘要

在对哥本哈根大鼠前列腺来源的肿瘤细胞系进行的体外研究中,这些细胞系的鸟氨酸脱羧酶(ODC)活性对α-二氟甲基鸟氨酸(α-DFMO)抑制的敏感性与正常前列腺组织相同。肿瘤在小牛血清中的体外生长受到ODC抑制剂α-甲基鸟氨酸和α-二氟甲基鸟氨酸的抑制。这种抑制作用被二胺氧化酶抑制剂氨基胍部分逆转。此外,α-DFMO对缺乏二胺氧化酶活性的血清中的这些细胞生长没有抑制作用,但添加二胺氧化酶后则具有抑制作用。

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