TY - JOUR
T1 - Comparative degradomics of porcine and human wound exudates unravels biomarker candidates for assessment of wound healing progression in trauma patients
AU - Sabino, Fabio Mira Rocha
AU - Egli, Fabian E
AU - Savickas, Simonas
AU - Holstein, Jörg
AU - Kaspar, Daniela
AU - Rollmann, Mika
AU - Kizhakkedathu, Jayachandran N
AU - Pohlemann, Tim
AU - Smola, Hans
AU - auf dem Keller, Ulrich
PY - 2017
Y1 - 2017
N2 - Impaired cutaneous wound healing is a major complication in elderly people and patients suffering from diabetes with raising rates in industrialized countries. Heterogeneity of clinical manifestations hampers effective molecular diagnostics and decisions for appropriate therapeutic regimens. Using a customized positional quantitative proteomics workflow, we have established a time-resolved proteome and N-terminome resource from wound exudates in a clinically relevant pig wound model that we exploited as robust template to interpret a heterogeneous dataset from patients undergoing the same wound treatment. With zyxin, IQGA1 and HtrA1, this analysis and validation by targeted proteomics identified differential abundances and proteolytic processing of proteins of epidermal and dermal origin as prospective biomarker candidates for assessment of critical turning points in wound progression. Thus, we demonstrate the possibility of using a fine-tuned animal wound model to bridge the translational gap as prerequisite for future extended clinical studies with large cohorts of individuals affected by healing impairments. Data are available via ProteomeXchange with identifier PXD006674.
AB - Impaired cutaneous wound healing is a major complication in elderly people and patients suffering from diabetes with raising rates in industrialized countries. Heterogeneity of clinical manifestations hampers effective molecular diagnostics and decisions for appropriate therapeutic regimens. Using a customized positional quantitative proteomics workflow, we have established a time-resolved proteome and N-terminome resource from wound exudates in a clinically relevant pig wound model that we exploited as robust template to interpret a heterogeneous dataset from patients undergoing the same wound treatment. With zyxin, IQGA1 and HtrA1, this analysis and validation by targeted proteomics identified differential abundances and proteolytic processing of proteins of epidermal and dermal origin as prospective biomarker candidates for assessment of critical turning points in wound progression. Thus, we demonstrate the possibility of using a fine-tuned animal wound model to bridge the translational gap as prerequisite for future extended clinical studies with large cohorts of individuals affected by healing impairments. Data are available via ProteomeXchange with identifier PXD006674.
U2 - 10.1016/j.jid.2017.08.032
DO - 10.1016/j.jid.2017.08.032
M3 - Journal article
C2 - 28899681
SN - 0022-202X
VL - 138
SP - 413
EP - 422
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
IS - 2
ER -