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胸苷磷酸化酶诱导癌细胞氧化应激并促进血管生成因子的分泌。

Thymidine phosphorylase induces carcinoma cell oxidative stress and promotes secretion of angiogenic factors.

作者信息

Brown N S, Jones A, Fujiyama C, Harris A L, Bicknell R

机构信息

Molecular Angiogenesis Laboratory, Imperial Cancer Research Fund, Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, United Kingdom.

出版信息

Cancer Res. 2000 Nov 15;60(22):6298-302.

Abstract

Thymidine phosphorylase (TP) (E.C. 2.4.2.4), also known as platelet-derived endothelial cell growth factor, is a potent angiogenic factor. The expression of TP correlates with poor prognosis in a range of tumor types. 2-Deoxy-D-ribose-1-phosphate, a product of thymidine catabolism by TP, is a strongly reducing sugar that generates oxygen radical species during the early stages of protein glycation. We show that thymidine induces oxidative stress in TP-overexpressing carcinoma cells, promoting secretion of the stress-induced angiogenic factors vascular endothelial growth factor and interleukin-8, and inducing matrix metalloproteinase-1. Our findings outline a putative mechanism for TP-induced angiogenesis and identify novel targets for intervention.

摘要

胸苷磷酸化酶(TP)(酶学委员会编号:2.4.2.4),也被称为血小板衍生内皮细胞生长因子,是一种强效血管生成因子。TP的表达与多种肿瘤类型的不良预后相关。2-脱氧-D-核糖-1-磷酸是TP催化胸苷分解代谢的产物,是一种强还原糖,在蛋白质糖基化早期会产生活性氧物种。我们发现胸苷在TP过表达的癌细胞中诱导氧化应激,促进应激诱导的血管生成因子血管内皮生长因子和白细胞介素-8的分泌,并诱导基质金属蛋白酶-1。我们的研究结果概述了TP诱导血管生成的一种假定机制,并确定了新的干预靶点。

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