Arginine metabolic pathways involved in the modulation of tumor-induced angiogenesis by macrophages

被引:38
作者
Davel, LE
Jasnis, MA
de la Torre, E
Gotoh, T
Diament, M
Magenta, G
de Lustig, ES
Sales, ME
机构
[1] Inst Oncol Angel H Roffo, RA-1417 Buenos Aires, DF, Argentina
[2] Kumamoto Univ, Sch Med, Dept Mol Genet, Kumamoto 860, Japan
关键词
tumor angiogenesis; macrophage; arginase; nitric oxide synthase; CD31;
D O I
10.1016/S0014-5793(02)03682-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neovascularization, an essential step for tumor progression and metastasis development, can be modulated by the presence of macrophages (Mps) in the tumor microenvironment. The ability of Mps to regulate the angiogenicity of the LMM3 tumor cell line was studied. Peritoneal Mps from LMM3 tumor-bearing mice (TMps) potentiate in vivo LMM3 angiogenicity. These results were confirmed by CD31 immunoblotting assays. The activity of TMps depended on nitric oxide synthase (NOS) and arginase (A) activity. By immunoblotting we evidenced that AI and All isoforms were up-regulated in TMps while the inducible and neuronal NOS isoforms; were highly expressed in normal Mps. TMps might positively modulate tumor growth by stimulating angiogenic cascade mainly through pollyamine synthesis. (C) 2002 Published by Elsevier Science B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:216 / 220
页数:5
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