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High levels of extracellular ATP lead to chronic inflammatory response in melanoma patients.

Authors :
Manica A
Da Silva AM
Cardoso AM
Moreno M
Leal DB
Dutra Da Silva A
Schetinger MRC
Morsch VMM
Bagatini MD
Source :
Journal of cellular biochemistry [J Cell Biochem] 2018 May; Vol. 119 (5), pp. 3980-3988. Date of Electronic Publication: 2018 Jan 22.
Publication Year :
2018

Abstract

Skin cancer represents a serious public health problem and melanoma is considered the most significant due to its high metastasis capacity. Evasion mechanisms are the main characteristic of these tumor cells to escape of immune response. Extracellular nucleotides and nucleosides play an important role in inflammatory and immune responses. In this study, we analyzed the expression and activity of purinergic system enzymes in platelets and lymphocytes, ATP levels quantification, as well the level of pro and anti-inflammatory interleukins in the serum of 23 patients with surgical melanoma removal (CM group) and 23 control subjects (CT group). Results showed a decrease in ATP, ADP, and AMP hydrolysis and an increase in ATP levels quantification in CM group. The pro-inflammatory cytokines were elevated in CM group when compared to CT group. These results suggest an inflammatory process, even after surgical removal, due to elevated extracellular ATP levels. Besides, CM group displayed an increase in IL-10 levels and an increased in ADA activity in platelets and lymphocytes. Once adenosine and IL-10 are anti-inflammatory molecules, these results indicate a down-regulation of immune system front to malignant process. The alteration in nucleotide and nucleoside hydrolysis reinforces the purinergic systems role in this cancer. Therefore, even after surgical removal, the purinergic system can develop a chronic inflammatory micro-environment that can influence directly on relapse or metastasis.<br /> (© 2017 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1097-4644
Volume :
119
Issue :
5
Database :
MEDLINE
Journal :
Journal of cellular biochemistry
Publication Type :
Academic Journal
Accession number :
29227546
Full Text :
https://doi.org/10.1002/jcb.26551