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Analysis of alpha-synuclein in malignant melanoma - development of a SRM quantification assay.

Authors :
Charlotte Welinder
Göran B Jönsson
Christian Ingvar
Lotta Lundgren
Bo Baldetorp
Håkan Olsson
Thomas Breslin
Melinda Rezeli
Bo Jansson
Thomas E Fehniger
Thomas Laurell
Elisabet Wieslander
Krzysztof Pawlowski
György Marko-Varga
Source :
PLoS ONE, Vol 9, Iss 10, p e110804 (2014)
Publication Year :
2014
Publisher :
Public Library of Science (PLoS), 2014.

Abstract

Globally, malignant melanoma shows a steady increase in the incidence among cancer diseases. Malignant melanoma represents a cancer type where currently no biomarker or diagnostics is available to identify disease stage, progression of disease or personalized medicine treatment. The aim of this study was to assess the tissue expression of alpha-synuclein, a protein implicated in several disease processes, in metastatic tissues from malignant melanoma patients. A targeted Selected Reaction Monitoring (SRM) assay was developed and utilized together with stable isotope labeling for the relative quantification of two target peptides of alpha-synuclein. Analysis of alpha-synuclein protein was then performed in ten metastatic tissue samples from the Lund Melanoma Biobank. The calibration curve using peak area ratio (heavy/light) versus concentration ratios showed linear regression over three orders of magnitude, for both of the selected target peptide sequences. In support of the measurements of specific protein expression levels, we also observed significant correlation between the protein and mRNA levels of alpha-synuclein in these tissues. Investigating levels of tissue alpha-synuclein may add novel aspect to biomarker development in melanoma, help to understand disease mechanisms and ultimately contribute to discriminate melanoma patients with different prognosis.

Subjects

Subjects :
Medicine
Science

Details

Language :
English
ISSN :
19326203
Volume :
9
Issue :
10
Database :
Directory of Open Access Journals
Journal :
PLoS ONE
Publication Type :
Academic Journal
Accession number :
edsdoj.0f591e4e97c74574808a4d15194e4850
Document Type :
article
Full Text :
https://doi.org/10.1371/journal.pone.0110804