Overexpression of G1/S cyclins and PCNA and their relationship to tyrosine phosphorylation and dephosphorylation during tumor promotion by metanil yellow and malachite green

被引:29
作者
Sundarrajan, M
Fernandis, AZ
Subrahmanyam, G
Prabhudesai, S
Krishnamurthy, SC
Rao, KVK [1 ]
机构
[1] Tata Mem Ctr, Cellular Carcinogenesis Lab, Canc Res Inst, Bombay 40012, Maharashtra, India
[2] Tata Mem Hosp, Dept Pathol, Tata Mem Ctr, Bombay 40012, Maharashtra, India
[3] Indian Inst Technol, Ctr Biotechnol, Bombay 400076, Maharashtra, India
关键词
N-nitrosodiethylamine (DEN); preneoplastic; metanil yellow (MY); malachite green (MG); phenobarbitone (PB); frank hepatocellular carcinoma; tyrosine phosphorylation; PCNA; cyclin D1; cyclin E;
D O I
10.1016/S0378-4274(00)00216-2
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Metanil yellow (MY) and Malachite green (MG) are textile dyes, which, despite the ban, occur unscrupulously as food colouring agents. Accordingly they constitute a serious public health hazard and are of sufficient environmental concern. We have earlier reported that both MY and MG have tumor promoting effects on the development of hepatic preneoplastic lesions induced by N-nitrosodielhylamine in rats. In order to understand the possible mechanism(s) by which metanil yellow (MY) and malachite green (MG) promotes liver tumor development, we have studied the tyrosine phosphorylation and protein phosphatases during tumor promotion. We have also investigated the possible overexpression of G1/S cyclins and PCNA during tumor promotion by MY and MG. The present investigation indicates that enhanced tyrosine phosphorylation is associated with no change in levers of tyrosine protein phosphatases. We have also observed an increase in the expression of PCNA and G1/S cyclins during tumor promotion. These factors collectively may contribute to the abnormal cell proliferation during tumor promotion by MY and MG. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:119 / 130
页数:12
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