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α-二氟甲基鸟氨酸抑制由一种促肿瘤大鼠尿液成分刺激的细胞生长。

alpha-Difluoromethylornithine inhibits cell growth stimulated by a tumor-promoting rat urinary fraction.

作者信息

Homma Y, Ozono S, Numata I, Seidenfeld J, Oyasu R

出版信息

Carcinogenesis. 1985 Jan;6(1):159-61. doi: 10.1093/carcin/6.1.159.

Abstract

The growth stimulating activity of a tumor-promoting rat urinary fraction (Fraction I), and its inhibition by alpha-difluoromethylornithine (DFMO) were examined in vitro using a rat bladder carcinoma cell line, 804G cells. Cell growth was markedly stimulated by Fraction I when added to the basic medium containing 0.2% fetal calf serum (FCS). The increased proliferative activity was associated with an increase in ornithine decarboxylase (ODC) activity and intracellular polyamine content. DFMO effectively inhibited the growth of 804G cells stimulated by Fraction I or by 10% FCS, and the inhibition was associated with suppression of ODC activity and partial depletion of intracellular putrescine and spermidine. Growth inhibition was reversed by exogenous putrescine. These results show that (i) urinary Fraction I, both a tumor promoter in bladder carcinogenesis and an ODC inducer in 804G cells, has potent mitogenicity in 804G cells, and (ii) the mitogenicity is inhibited by DMFO, an irreversible inhibitor of ODC.

摘要

利用大鼠膀胱癌细胞系804G细胞在体外检测了一种促肿瘤大鼠尿液组分(组分I)的生长刺激活性及其被α-二氟甲基鸟氨酸(DFMO)抑制的情况。当将组分I添加到含有0.2%胎牛血清(FCS)的基础培养基中时,细胞生长受到显著刺激。增殖活性的增加与鸟氨酸脱羧酶(ODC)活性及细胞内多胺含量的增加相关。DFMO有效抑制了由组分I或10% FCS刺激的804G细胞的生长,这种抑制与ODC活性的抑制以及细胞内腐胺和亚精胺的部分耗竭相关。外源性腐胺可逆转生长抑制。这些结果表明:(i)尿液组分I,既是膀胱致癌作用中的肿瘤促进剂,也是804G细胞中的ODC诱导剂,在804G细胞中具有强大的促有丝分裂活性;(ii)这种促有丝分裂活性被ODC的不可逆抑制剂DMFO所抑制。

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