Nitric oxide differentially regulates pro- and anti-angiogenic markers in DLD-1 colon carcinoma cells.

Abstract:

:Inducible nitric oxide (NO) synthase (iNOS) appears to be a marker of tumor progression in colon carcinogenesis. Here we investigated effects of NO on selected chemokines that differentially regulate angiogenesis, namely pro-angiogenic interleukin (IL)-8 as well as tumor-suppressive interferon-inducible protein-10 (IP-10) and monokine induced by interferon-gamma (MIG). These chemokines are expressed by DLD-1 colon carcinoma cells after stimulation with IL-1beta/interferon-gamma. Expression of IL-8 was markedly upregulated by NO. Moreover, NO enhanced expression of vascular endothelial growth factor (VEGF). In contrast, expression of IP-10 and MIG was suppressed by NO. The present data are consistent with previous observations that link NO to enhanced tumor angiogenesis and imply that NO-mediated upregulation of IL-8 and VEGF as well as downregulation of IP-10 and MIG may contribute to this phenomenon.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Hellmuth M,Paulukat J,Ninic R,Pfeilschifter J,Mühl H

doi

10.1016/S0014-5793(04)00275-3

keywords:

subject

Has Abstract

pub_date

2004-04-09 00:00:00

pages

98-102

issue

1-3

eissn

0014-5793

issn

1873-3468

pii

S0014579304002753

journal_volume

563

pub_type

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