Suppr超能文献

生长支持性多胺类似物1,12 - 二甲基精胺可显著诱导亚精胺/精胺N1 - 乙酰转移酶,且无细胞毒性。

Significant induction of spermidine/spermine N1-acetyltransferase without cytotoxicity by the growth-supporting polyamine analogue 1,12-dimethylspermine.

作者信息

Yang J, Xiao L, Berkey K A, Tamez P A, Coward J K, Casero R A

机构信息

Oncology Center, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, USA.

出版信息

J Cell Physiol. 1995 Oct;165(1):71-6. doi: 10.1002/jcp.1041650109.

Abstract

The superinduction of the polyamine catabolic enzyme spermidine/spermine N1-acetyltransferase (SSAT) has been implicated in the cell type-specific cytotoxic activity of some polyamine analogues. We now report that one polyamine analogue, 1,12-dimethylspermine (DMSpm), produces a large induction of SSAT with no significant effects on growth in the human large cell lung carcinoma line, NCl H157. This cell line has been demonstrated to respond to other analogues with SSAT superinduction and cell death. Treatment of the lung cancer cell line with DMSpm produces a rapid increase in SSAT activity and a near complete depletion of the natural polyamines. Additionally, DMSpm supports cell growth in cells which have been depleted of their natural polyamines by the ornithine decarboxylase inhibitor, 2-difluoromethylornithine. The current results suggest that significant induction of SSAT can occur in the absence of cytotoxicity when the inducing polyamine analogue can support growth and that increased SSAT activity alone is not sufficient for cytotoxicity to occur.

摘要

多胺分解代谢酶亚精胺/精胺N1 - 乙酰基转移酶(SSAT)的超诱导与某些多胺类似物的细胞类型特异性细胞毒性活性有关。我们现在报告,一种多胺类似物1,12 - 二甲基精胺(DMSpm)在人肺大细胞癌系NCl H157中可大量诱导SSAT,而对生长无显著影响。该细胞系已被证明对其他类似物有SSAT超诱导和细胞死亡反应。用DMSpm处理肺癌细胞系会使SSAT活性迅速增加,并使天然多胺几乎完全耗尽。此外,DMSpm能支持那些已被鸟氨酸脱羧酶抑制剂2 - 二氟甲基鸟氨酸耗尽天然多胺的细胞的生长。目前的结果表明,当诱导性多胺类似物能支持生长时,在无细胞毒性的情况下也可发生显著的SSAT诱导,且仅SSAT活性增加不足以导致细胞毒性发生。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验