We saw a clear trend towards higher concentrations of cβigH3 for degraded matrices generated with TGF-β treatment (mean = 11.7 nM) compared to matrices generated without TGF-β treatment (mean = 4.3 nM) (Fig. 2 ), indicating that cβigH3 is associated with degradation of fibrotic matrices. cβigH3 could be detected in serum from patients with different types of cancer We measured cβigH3 in serum from cohort 1.
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Proteolytic degradation of Beta-Ig H3 (βigH3/TGFBI) can be quantified non-invasively in serum and predicts prognosis in patients with advanced pancreatic ductal adenocarcinoma.
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