Serum activity of DPPIV and its expression on lymphocytes in patients with melanoma and in people with vitiligo
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Abstract
Background: Dipeptidyl peptidase IV, a multifunctional serine protease, is implicated in regulation of malignant
transformation, promotion and further progression of cancer, exerting tumor-suppressing or even completely
opposite - tumor-promoting activities.
The aim of present research was to determine the serum DPPIV activity, as well as the percentages of CD26+
lymphocytes, CD26+ overall white blood cells and the mean fluorescence intensity of CD26 expression on
lymphocytes in patients with melanoma, people with vitiligo and in healthy controls.
Methods: The activity of DPPIV in serum was determined by colorimetric test. Expression of DPPIV (as CD26) on
immunocompetent peripheral white blood cells was done using flow cytometry analysis.
Results: Data from our study show for the first time statistically significant decrease: in the serum DPPIV activity, in
the percentage of CD26+ overall white blood cells and in the percentage of lymphocytes in patients with
melanoma in comparison to healthy control people. In addition, significantly lower serum DPPIV activity was found
in the group of patients with melanoma in relation to people with vitiligo too.
Conclusion: This study indicates the need for exploring the cause and the importance of the disturbances in the
serum DPPIV activity and in the CD26 expression on immunocompetent cells in complex molecular mechanisms
underlying the development and progression of melanoma
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Matić, I. Z., Đorđić, M., Grozdanić, N., Damjanović, A., Kolundžija, B., Erić-Nikolić, A., ... & Rašković, S. (2012). Serum activity of DPPIV and its expression on lymphocytes in patients with melanoma and in people with vitiligo. BMC immunology, 13(1), 48.
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https://doi.org/10.1186/1471-2172-13-48Sponsors
The authors are grateful to the Ministry of Education and Science of the Republic of Serbia for the financial support (Project 175011)
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© 2012 Matić et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.



