Comparative analysis of affected and unaffected areas of systemic sclerosis skin biopsies by high-throughput proteomic approaches
Arthritis Research & Therapy volume 22, Article number: 107 (2020)
Pathogenesis and aetiology of systemic sclerosis (SSc) are currently unclear, thus rendering disease prognosis, diagnosis and treatment challenging. The aim of this study was to use paired skin biopsy samples from affected and unaffected areas of the same patient, in order to compare the proteomes and identify biomarkers and pathways which are associated with SSc pathogenesis.
Biopsies were obtained from affected and unaffected skin areas of SSc patients. Samples were cryo-pulverised and proteins were extracted and analysed using mass spectrometry (MS) discovery analysis. Differentially expressed proteins were revealed after analysis with the Progenesis QIp software. Pathway analysis was performed using the Enrichr Web server. Using specific criteria, fifteen proteins were selected for further validation with targeted-MS analysis.
Proteomic analysis led to the identification and quantification of approximately 2000 non-redundant proteins. Statistical analysis showed that 169 of these proteins were significantly differentially expressed in affected versus unaffected tissues. Pathway analyses showed that these proteins are involved in multiple pathways that are associated with autoimmune diseases (AIDs) and fibrosis. Fifteen of these proteins were further investigated using targeted-MS approaches, and five of them were confirmed to be significantly differentially expressed in SSc affected versus unaffected skin biopsies.
Using MS-based proteomics analysis of human skin biopsies from patients with SSc, we identified a number of proteins and pathways that might be involved in SSc progression and pathogenesis. Fifteen of these proteins were further validated, and results suggest that five of them may serve as potential biomarkers for SSc.
Systemic sclerosis (SSc), also known as scleroderma, refers to a systemic rheumatic disease that is generally classified as an autoimmune disease (AID) [1, 2]. It is characterised by the three main pathological hallmarks: vasculopathy, immune system abnormalities and excessive deposition of collagen (fibrosis) in many tissues throughout the human body causing hardening and thickening [1, 3]. This disease is heterogeneous and multisystemic as symptoms vary among patients and several organs of the human body might be affected .
Based on its clinical features, SSc is subdivided into limited cutaneous SSc (lcSSc) and diffused cutaneous SSc (dcSSc) . LcSSc is less severe than dcSSc as skin thickening is usually limited to the distal extremities, finger, upper neck and face. However, in some cases, lcSSc patients present mild organ-complications. In contrast to lcSSc, dcSSc progresses faster and usually affects internal organs (e.g. lung, kidney and heart) causing complications such as congestive heart failure, renal crisis and interstitial lung disease (ILD). In addition, serological data showed that different autoantibodies are produced in each subtype [3, 4]. Anti-centromere autoantibodies (ACA) are mainly present in lcSSc patients, whereas anti-topoisomerase (ATA) and anti-RNA-polymerase (ARNAP) autoantibodies in dcSSc patients .
Up to date, SSc aetiopathogenesis is not well understood; thus, its prognosis and diagnosis are challenging and there is no cure for the disease . Therefore, there is an urgent requirement for SSc biomarkers that could be used not only for prognosis and diagnosis of the disease, but also for SSc staging, activity, classification and for potential therapeutic targets. During the last two decades, proteomics biomarker discovery has been developed due to the advances of mass spectrometry (MS) approaches. MS, a high-throughput technique, enables the identification and quantification of proteins in a variety of biological samples such as saliva, plasma and serum .
The aim of this proteomic study was to analyse affected and unaffected skin biopsy samples from patients with SSc in order to identify biomarkers and pathways which are implicated in SSc pathogenesis. We hereby report some associated pathways and the validation of possible SSc proteomic biomarkers.
Materials and methods
Fourteen paired cutaneous biopsies were obtained from clinically affected (forearm) and clinically unaffected (proximal arm) skin from seven patients with SSc, voluntarily participating in the PRECISESADs project (ref: 115565) following the appropriate written informed consent procedures. The study was approved by the Ethical Committee of Université catholique de Louvain (2014/17DEC/603) and the Cyprus National Bioethics committee (ΕΕΒΚ/ΕΠ/2015/31). All patients fulfilled the LeRoy and Medsger criteria  and were in the active phase of the disease.
Histological classification of skin biopsy samples
Histological features of SSc skin biopsies (collagen bundles and inflammatory cells levels) were assessed.
Evaluation of optical parameters (density of collagen bundles and inflammatory cell infiltrates) was performed using a semi-quantitative score on a 0–3 scale, where 0 indicates absence, 1 weak and very focal staining, 2 moderate and focal staining, and 3 moderate in several foci. Perivascular fibroblastic densification was assessed as present or not .
Pre-analytical sample processing
Frozen skin biopsies were cryo-pulverised to a fine powder using a cell crusher device (Cellcrusher, Cork). Skin powdered samples were suspended in a lysis buffer (10 mM Tris-HCl pH 7.4; 150 mM NaCl; 1 mM EDTA; PBS; 0.2% SDS; Proteinase Inhibitor (Roche, USA)) and homogenised by sonication. Then, protein precipitation was performed using 1 ml of frozen acetone at − 20°C, overnight. Protein pellet was re-suspended in urea buffer, and total protein content was determined by the BCA assay. A total of 100 μg of protein was transferred to centrifugal filter units (30 kDa MWCO, Pall NanoSep Omega, OD030C34, Sigma Aldrich), and a modified filter-aided sample preparation (FASP) protocol  was followed. Briefly, proteins were reduced with 8 mM dithiothreitol at 56°C for 15 min, alkylated with 50 mM iodoacetamide at room temperature for 20 min in the dark and then digested with trypsin (Proteomics Grade, Roche Life Science, USA) at 1: 50 (trypsin: protein) ratio for 18 h at 37°C. Tryptic peptides were collected by centrifugation, and trifluoroacetic acid (TFA) was added to a final concentration of 0.5% to stop enzymatic reaction. TFA concentration was reduced to 0.1%, and peptides were purified and desalted by solid phase extraction using Sep-pak®Vac1cc (100 mg) tC18 cartridges (Waters, Ireland). The eluted peptides were dried, using centrifuge vacuum at 45°C and stored in − 80 °C until further analysis.
Dried peptide pellets were re-suspended in buffer (99% H2O, 1% acetonitrile, 0.1% formic acid). The total peptide concentration was determined by absorption at 280 nm (A280) and was adjusted accordingly to a final concentration of 0.2 μg/μl prior liquid chromatography-mass spectrometry (LC-MS) analysis. For the discovery phase, 2 μl was loaded onto an analytical column (nanoAcquity CSH C18 75 μm ID X 250 mm length, 1.7 μm particle size, 130 Å pore size, Waters, UK) and separated on a nano-liquid chromatography (LC) system (nanoAcquity UPLC, Waters, UK) at a flow rate of 0.300 μl/min using a 220-min gradient elution. Column oven temperature was set to 40°C. Eluted peptides were ionised in positive mode using nanoelectrospray ionisation (nanoESI) and analysed on a Waters Synapt G2Si HDMS instrument operated in ion mobility mode, using an ultra-definition (UD) MSe approach .
For the validation phase, the MRM (Multiple Reaction Monitoring) analyses were performed using specific selected analytes. In the first step, a pool of selected synthetic peptides (2.5 μg) was loaded onto the analytical column and separated as descripted in the discovery phase using a 125-min gradient elution and the column oven temperature was set to 45°C. For the skin biopsy samples, 10 μl of 0.8 μg/μl total peptide concentration were loaded. Peptides were analysed on a Waters Xevo TQD instrument operated on positive MRM mode.
Protein identification and quantification and statistical analyses (discovery phase)
Raw MS data were processed by the Progenesis QI for proteomics (QIp) analysis software. Peptide identifications were performed using the MSe  search identification, with 1% peptide false discovery rate (FDR). The resulted identifications were further refined using the following parameters: confidence score ≥ 5, sequence length ≥ 6 and hits ≥ 2. Protein-level relative quantitation was performed using the Hi-N approach (N = 3) as implemented in the Progenesis QIp. Further statistical analysis was carried out according to affected/unaffected paired samples (all affected versus all unaffected skin biopsy samples), and this is referred to as affected/unaffected comparison in this manuscript. A variation of one-way ANOVA analysis, as implemented in the Progenesis QIp software, was used to calculate p values. Data normalisation was performed by Progenesis QIp software, using the ‘normalise to all compounds’ option. Briefly, the normalisation approach is based on the calculation of a global scaling factor which is then applied to normalise samples to an automatically selected reference sample.
Selection of proteins for the validation phase
Selection of proteins for validation was performed based on p value and FC through the affected/unaffected comparison. Significantly differentially expressed proteins (p < 0.05) with FC > 2.5 or < 0.4 in affected/unaffected comparison were selected.
Synthesised peptides for validation
For the validation phase, selection of target peptides for proteins quantification was performed using the Skyline 4.1 source (MacCross Lab software, University of Washington, WA, USA) . At least two unique peptides were selected for each protein of interest. Synthesised label-free peptides (~ 70% purity) were purchased from GenScript Biotech, Netherlands. The targeted MS method parameters used for each peptide are shown in Additional file 1.
MRM-MS data and statistical analyses
The transition list of targeted peptides was created by the Skyline 4.1 source. The peak areas of peptides were calculated by summing the peak areas of their transition ions.
Statistical analysis of validation data was carried out using two-tailed paired t test for paired samples analysis (all affected versus all unaffected skin biopsy samples). A p value of < 0.05 was considered as significant. For each protein, the peptide with the strongest p value was indicated as quantitative, while the rest were used as qualitative references. The FC was calculated by comparing the mean value of the peak areas of the peptide among the grouped samples.
The Uniprot Retrieve/ ID mapping tool (http://www.uniprot.org/uploadlists/) was used to convert the UniProtKB AC/ID to Gene Name.
Pathway analysis was performed for significantly over-expressed (p < 0.05, FC > 1.5) or under-expressed (p < 0.05, FC < 0.67) proteins from affected/unaffected comparison in the discovery phase. Enrichr (http://amp.pharm.mssm.edu/Enrichr/) was utilised for inferring pathway knowledge about the gene set corresponding to the differentially expressed proteins, based on KEGG 2019.
Volcano plots were carried out using the R studio software (version 1.1.442, 2018-03-11). The volcano plot indicates the -log10 (p value) for proteins plotted against their respective log2 (fold change (FC)) on the y and x axes, respectively.
Skin biopsy samples
Five female and two male unrelated SSc patients were analysed with a mean ± SD age of 56 ± 15.80 years and 38.5 ± 9.20 years, respectively. Skin biopsies were histologically assessed, and their features are shown in Additional file 2.
Discovery proteomic analysis
Discovery phase proteomic analysis of the analysed SSc samples led to the identification and quantification of 2149 proteins. Samples were grouped and compared based on affected/unaffected skin biopsy areas. This comparison showed that 169 (87 under-expressed and 82 over-expressed) out of 2149 identified proteins were significantly differentially expressed (p < 0.05) (Additional file 3) (Table 1).
Pathway analysis of significantly over-expressed (p < 0.05, FC > 1.5) and under-expressed (p < 0.05, FC < 0.67) proteins from affected/unaffected comparison revealed a large number of involved pathways. Significant extracted pathways (p < 0.05) are shown in Table 2. Several pathways that are associated with SSc pathogenesis were also identified in this study. Platelet activation, ECM-receptor interaction, complement and coagulation cascades, antigen processing and presentation and leukocyte transendothelial migration are among these significant extracted pathways (Table 2).
Selected proteins and validation
Although many of the dysregulated proteins could be promising biomarkers for SSc, a limited number of proteins were selected for validation due to the high cost of MRM-MS approach. A total number of 15 proteins were selected for validation through the affected/unaffected comparison (Fig. 1).
Five (UCHL1, PPID, DDX55, COX6B1 and APCS) out of these proteins were confirmed in the validation phase to be significantly dysregulated in affected/unaffected comparison and all details and results are shown in Table 1. UCHL1 belongs to the ubiquitin C-terminal hydrolases family and enables the hydrolysis of small ubiquitin adducts . PPID (CyP40) is implicated in protein folding, nuclear localisation of progesterone, oestrogen and glucocorticoid receptors, ligand binding, pro-tumorigenic effects and congenital heart defects [15, 16]. DDX55 belongs to the DEAD-box proteins which are implicated in several RNA metabolism processes such as RNA transcription, degradation as well as gene expression in organelles and pre-mRNA splicing . COX6B1 is a subunit of Complex IV and Massa et al. reported that a recessive mutation on COX6B1 causes a mitochondrial encephalomyopathy . The last confirmed protein is the plasma glycoprotein APCS which functions as a calcium-dependent lectin  and is involved in immunological responses .
SSc is a multisystemic AID with unclear aetiology and pathogenesis. The main pathological features of the disease, vasculopathy, inflammation and fibrosis, highlight its complexity and indicate that various molecules and pathways are implicated in the different stages of disease pathogenesis. However, these molecules and pathways/mechanisms have not been fully elucidated . Therefore, the aim of this study was to analyse skin biopsies from affected and unaffected areas of the same SSc patients in order to study different stages of the disease and identify sensitive proteomic biomarkers gaining insights into the pathways/mechanisms that are implicated in SSc pathogenesis.
Using discovery MS proteomic analysis of SSc samples, 2149 proteins were identified and 169 proteins were shown to be significantly dysregulated in the affected/unaffected comparison. Pathway analysis of these proteins confirmed the heterogeneity of the disease as the proteins are involved in approximately 190 different pathways. As SSc is an extremely complex disease and several molecules, cell types and biological processes are implicated in its pathogenesis , several of the bioinformatics-highlighted pathways might be associated with the disease in different ways. Furthermore, some of these pathways are related with other diseases including AIDs. These findings indicate that several diseases especially AIDs might share common pathogenetic mechanisms. According to the Enrichr analyses, platelet activation, ECM-receptor interaction, complement and coagulation cascades, antigen processing and presentation and leukocyte transendothelial migration are among the common significant extracted pathways.
It is known that overexpression of the ECM proteins plays a key role in the development of fibrosis in SSc . Our data confirm this knowledge as three proteins (ITGB1, VTN and ITGA5) that are implicated in ECM-receptor interaction pathway were over-expressed in the affected/unaffected comparison. Proteins that are implicated in complement and coagulation cascades (C4B, VTN, SERPINC1 and CLU), and antigen processing and presentation pathways (HSPA4 and HLA-G) were also significantly over-expressed in this comparison. Although this observation is consistent with the results obtained in a previous study, these pathways are not only activated in SSc but also in other AIDs [23, 24]. Another important pathway that was extracted from ITGB1, AKT3 and MYLK over-expressed proteins in the affected/unaffected comparison is the platelet activation pathway which contributes to all three stages of SSc pathogenesis: vascular injury, inflammation and fibrosis . In a previous study, Agache et al. reported that platelet activation markers are associated with the severity and activity of the disease and increased levels of C-reactive protein (CRP) . Leukocyte transendothelial migration is also an essential pathway as CD4+ T lymphocytes transendothelial migration is enhanced in this disease and the migrating cells display an activated phenotype . The ITGB1, ACTN1 and ICAM1 proteins that were identified to be significantly over-expressed in affected/unaffected comparison in our study are implicated in this pathway.
As already stated, a large number of proteins were identified; however, only 15 proteins were selected for validation due to the high cost of MS. In the validation phase, 5 (UCHL1, PPID, DDX55, COX6B1 and APCS) out of these 15 selected proteins were further confirmed to be significantly dysregulated. Giusti et al. in a transcriptomic study showed that ubiquitin C-terminal hydrolases protein UCHL1 and other molecules that are implicated in ubiquitination/stress are highly expressed in skin endothelial cells of dcSSc patients compared to controls [14, 28]. In the validation phase of our study, UCHL1 was confirmed to be significantly over-expressed in affected/unaffected comparison. It is remarkable that overexpression of UCHL1 in SSc affected skin areas is confirmed both at the transcriptome and proteome levels by two independent studies. CyP40 is another protein that was found to be significantly over-expressed in the affected/unaffected comparison in our study. Interestingly, Balanescu et al. showed that cyclophilin-A, a member of the same family with CyP40, is abnormally expressed in biological fluids and cutaneous biopsies of SSc patients . These evidences suggest that UCHL1 and CyP40 could be promising SSc biomarkers and further studies on these two molecules should be performed. DDX55 and COX6B1 were also significantly over-expressed in the affected/unaffected comparison. These two proteins have been associated with SSc for the first time in our study; thus, additional investigation should be performed in order to further confirm their association with the development of SSc and their potential use as biomarkers of the disease. APCS is a plasma glycoprotein which is implicated in immunological responses . Tennent et al. used serum of lcSSc and dcSSc patients and 12-month longitudinal patients and showed that APCS levels were in the normal range; except from a limited number of elevated values that are associated with acute inter-current complications . Aden et al. showed that the APCS precursor level was significantly overexpressed in skin biopsies from SSc patients compared to healthy controls . In agreement with Aden et al., our study showed that APCS is significantly over-expressed in the affected/unaffected comparison in both the discovery and validation phases. However, this protein may generally be associated with autoimmunity instead of specifically with SSc as it was found to be implicated in other AIDs as well .
This study shows different proteomic background and histological features among affected and unaffected skin biopsies of the same SSc patients. This is the first study that compares SSc skin areas macroscopically classified as affected and unaffected. Despite the importance of the results, the small number of samples used is a limitation of this study. However, previous reported studies also had this limitation [32, 33], because SSc is a rare disease, and thus, large numbers of patients are not expected to be recruited. Although skin biopsies were obtained only from SSc patients and not from healthy controls, this could be also considered as an advantage as the comparison is performed on samples from the same individual and the bias of heterogeneity is reduced.
In conclusion, the results of this study are important as they display the promising diagnostic power of a multi-biomarker approach. Pathway analysis showed that several pathways are implicated/activated in SSc pathogenesis. Available literature on UCHL1 and PPID proteins supports that they could be promising biomarkers for SSc. Interestingly, 3 (DDX55, PPID and COX6B1) out of 5 confirmed proteins have been associated with SSc for the first time in our study; therefore, these proteins could be novel biomarkers of the disease. In addition, APCS is associated with several AIDs and inflammatory pathways; thus, it might not be specific for SSc. However, they could be used as inflammation-related biomarkers. Further studies could be performed using samples from patients with different AID in order to assess whether these molecules are mainly associated with any other specific AID or with general inflammatory conditions. Further evaluation/validation studies could be performed in samples of new patients with SSc in order to confirm that these 5 molecules could be also useful biomarkers for specific stages (e.g. early phase) of the disease. Moreover, confirmation of these biomarkers in an easily accessible tissue will be useful for the clinicians and alleviate painful procedures for the SSc patients.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Diffused cutaneous SSc
Filter-aided sample preparation
False discovery rate
Interstitial lung disease
Liquid chromatography-mass spectrometry
Limited cutaneous SSc
Multiple reaction monitoring
Peripheral blood mononuclear cells
Systemic lupus erythematosus
Nguyen C, Bérezné A, Baubet T, Mestre-Stanislas C, Rannou F, Papelard A, et al. Association of gender with clinical expression, quality of life, disability, and depression and anxiety in patients with systemic sclerosis. PloS one. 2011;6(3):e17551-e.
Gorlova O, Martin JE, Rueda B, Koeleman BP, Ying J, Teruel M, et al. Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. PLoS Genet. 2011;7(7):14.
Saketkoo LA, Magnus JH, Doyle MK. The primary care physician in the early diagnosis of systemic sclerosis: the cornerstone of recognition and hope. Am J Med Sci. 2014;347(1):54–63.
Allanore Y, Simms R, Distler O, Trojanowska M, Pope J, Denton CP, et al. Systemic sclerosis. Nat Rev Dis Primers. 2015;1(15002):2.
Ho KT, Reveille JD. The clinical relevance of autoantibodies in scleroderma. Arthritis Res Ther. 2003;5(2):80–93 Epub 2003/02/12.
Chairta P, Nicolaou P, Christodoulou K. Genomic and genetic studies of systemic sclerosis: a systematic review. Hum Immunol. 2017;78(2):153–65.
Balanescu P, Ladaru A, Balanescu E, Baicus C, Dan GA. Systemic sclerosis biomarkers discovered using mass-spectrometry-based proteomics: a systematic review. Biomarkers. 2014;19(5):345–55.
LeRoy EC, Medsger TA Jr. Criteria for the classification of early systemic sclerosis. J Rheumatol. 2001;28(7):1573–6.
Galant C, Marchandise J, Stoenoiu MS, Ducreux J, De Groof A, Pirenne S, et al. Overexpression of ubiquitin-specific peptidase 15 in systemic sclerosis fibroblasts increases response to transforming growth factor β. Rheumatology. 2019;58(4):708–18.
Potriquet J, Laohaviroj M, Bethony JM, Mulvenna J. A modified FASP protocol for high-throughput preparation of protein samples for mass spectrometry. PloS one. 2017;12(7):e0175967.
Distler U, Kuharev J, Navarro P, Levin Y, Schild H, Tenzer S. Drift time-specific collision energies enable deep-coverage data-independent acquisition proteomics. Nat Methods. 2014;11(2):167–70.
Geromanos SJ, Vissers JP, Silva JC, Dorschel CA, Li GZ, Gorenstein MV, et al. The detection, correlation, and comparison of peptide precursor and product ions from data independent LC-MS with data dependant LC-MS/MS. Proteomics. 2009;9(6):1683–95.
MacLean B, Tomazela DM, Shulman N, Chambers M, Finney GL, Frewen B, et al. Skyline: an open source document editor for creating and analyzing targeted proteomics experiments. Bioinformatics. 2010;26(7):966–8.
Wada H, Kito K, Caskey LS, Yeh ET, Kamitani T. Cleavage of the C-terminus of NEDD8 by UCH-L3. Biochem Biophys Res Commun. 1998;251(3):688–92.
Jandova J, Janda J, Sligh JE. Cyclophilin 40 alters UVA-induced apoptosis and mitochondrial ROS generation in keratinocytes. Exp Cell Res. 2013;319(5):750–60 Epub 2012/12/03.
Perrucci GL, Gowran A, Zanobini M, Capogrossi MC, Pompilio G, Nigro P. Peptidyl-prolyl isomerases: a full cast of critical actors in cardiovascular diseases. Cardiovasc Res. 2015;106(3):353–64.
Linder P. Dead-box proteins: a family affair--active and passive players in RNP-remodeling. Nucleic Acids Res. 2006;34(15):4168–80.
Massa V, Fernandez-Vizarra E, Alshahwan S, Bakhsh E, Goffrini P, Ferrero I, et al. Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase. Am J Hum Genet. 2008;82(6):1281–9 Epub 2008/05/30.
Emsley J, White HE, O'Hara BP, Oliva G, Srinivasan N, Tickle IJ, et al. Structure of pentameric human serum amyloid P component. Nature. 1994;367(6461):338–45.
Gewurz H, Zhang XH, Lint TF. Structure and function of the pentraxins. Curr Opin Immunol. 1995;7(1):54–64.
Pattanaik D, Brown M, Postlethwaite BC, Postlethwaite AE. Pathogenesis of systemic sclerosis. Front Immunol. 2015;6:272.
Corallo C, Santucci A, Bernardini G, Figura N, Leoncini R, Riolo G, et al. Proteomic investigation of dermal fibroblasts isolated from affected and unaffected skin samples from patients with limited cutaneous systemic sclerosis: 2 distinct entities? J Rheumatol. 2017;44(1):40–8.
Chen M, Dittmann A, Kuhn A, Ruzicka T, von Mikecz A. Recruitment of topoisomerase I (Scl-70) to nucleoplasmic proteasomes in response to xenobiotics suggests a role for altered antigen processing in scleroderma. Arthritis Rheum. 2005;52(3):877–84.
Okrój M, Johansson M, Saxne T, Blom AM, Hesselstrand R. Analysis of complement biomarkers in systemic sclerosis indicates a distinct pattern in scleroderma renal crisis. Arthritis Res Ther. 2016;18(1):267.
Ramirez GA, Franchini S, Rovere-Querini P, Sabbadini MG, Manfredi AA, Maugeri N. The role of platelets in the pathogenesis of systemic sclerosis. Front Immunol. 2012;3:160.
Agache I, Radoi M, Duca L. Platelet activation in patients with systemic scleroderma--pattern and significance. Rom J Intern Med. 2007;45(2):183–91.
Stummvoll GH, Aringer M, Grisar J, Steiner CW, Smolen JS, Knobler R, et al. Increased transendothelial migration of scleroderma lymphocytes. Ann Rheum Dis. 2004;63(5):569–74.
Giusti B, Fibbi G, Margheri F, Serrati S, Rossi L, Poggi F, et al. A model of anti-angiogenesis: differential transcriptosome profiling of microvascular endothelial cells from diffuse systemic sclerosis patients. Arthritis Res Ther. 2006;8(4):19.
Tennent GA, Dziadzio M, Triantafillidou E, Davies P, Gallimore JR, Denton CP, et al. Normal circulating serum amyloid P component concentration in systemic sclerosis. Arthritis Rheum. 2007;56(6):2013–7.
Aden N, Shiwen X, Aden D, Black C, Nuttall A, Denton CP, et al. Proteomic analysis of scleroderma lesional skin reveals activated wound healing phenotype of epidermal cell layer. Rheumatology. 2008;47(12):1754–60.
Bickerstaff MC, Botto M, Hutchinson WL, Herbert J, Tennent GA, Bybee A, et al. Serum amyloid P component controls chromatin degradation and prevents antinuclear autoimmunity. Nat Med. 1999;5(6):694–7.
Bogatkevich GS, Ludwicka-Bradley A, Singleton CB, Bethard JR, Silver RM. Proteomic analysis of CTGF-activated lung fibroblasts: identification of IQGAP1 as a key player in lung fibroblast migration. Am J Physiol Lung Cell Mol Physiol. 2008;295(4):L603–L11 Epub 2008/08/01.
Del Galdo F, Shaw MA, Jimenez SA. Proteomic analysis identification of a pattern of shared alterations in the secretome of dermal fibroblasts from systemic sclerosis and nephrogenic systemic fibrosis. Am J Pathol. 2010;177(4):1638–46 Epub 2010/08/19.
The authors would like to thank (a) all SSc patients for their participation in the study, (b) the EU/EFPIA/Innovative Medicines Initiative Joint Undertaking PRECISESADS grant no. 115565, the Cyprus Institute of Neurology and Genetics and the Université catholique de Louvain for the support.
This work has received funding support from the EU/EFPIA/Innovative Medicines Initiative Joint Undertaking PRECISESADS grant no. 115565.
Ethics approval and consent to participate
The study was approved by the Ethical Committee of Université catholique de Louvain (2014/17DEC/603) and the Cyprus National Bioethics committee (ΕΕΒΚ/ΕΠ/2015/31) and conducted in accordance with the 1964 Declaration of Helsinki.
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The authors declare that they have no competing interests.
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MRM transitions used for the selected proteins analysis. This table shows the selected proteins/peptides for validation and the instrumental parameters used for peptide monitoring. Peptides highlighted in bold were used as the quantitative reference whereas the remaining peptides were used as qualitative references.
Clinical features of patients with SSc and histological features of SSc skin biopsy samples.
Significantly differentially expressed proteins (p < 0.05) in affected/unaffected comparison. Red and green font colour indicates proteins with FC ≥ 1.5 and FC ≤ 0.67 in affected compared to unaffected samples.
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Cite this article
Chairta, P., Nicolaou, P., Sokratous, K. et al. Comparative analysis of affected and unaffected areas of systemic sclerosis skin biopsies by high-throughput proteomic approaches. Arthritis Res Ther 22, 107 (2020). https://doi.org/10.1186/s13075-020-02196-x
- Systemic sclerosis
- Mass spectrometry
- Skin biopsy