| Literature DB >> 26190421 |
Darko Jurisic1, Igor Erjavec2, Vladimir Trkulja3, Ivo Dumic-Cule2, Irzal Hadzibegovic4, Lucija Kovacevic2, Tomo Svagusa2, Zdenko Stanec5, Slobodan Vukicevic2, Lovorka Grgurevic2.
Abstract
Type III transforming growth factor (TGFβ) receptor (TGFβrIII) modulates TGFβ superfamily signaling. Its tumor tissue expression is downregulated in human breast cancer. We determined (indirect ELISA) plasma levels of the soluble receptor (sTGFβrIII) in 47 women with breast cancer (AJCC stages 0-IIB) (cases) pre-surgery and over two months after the surgery, and in 36 healthy women (controls). Plasma sTBFβrIII was lower in cases than in the controls (age-adjusted difference -29.7 ng/mL, p < 0.001), and discriminated between disease and health (sensitivity and specificity 100% at 16.6 ng/mL). With adjustment for age, AJCC stage, lymph node involvement, HER2 and hormone receptor status, higher pre-surgery sTBFβrIII was associated with better progression-free survival (HR = 0.68, 95%CI 0.49-0.89, p = 0.004). An increasing trend in plasma sTBFβrIII was observed over 2 months after the surgery (0.6% increase/day, p < 0.001), consistently across the patient subsets. Data suggest a high potential of plasma sTBFβrIII as a novel diagnostic and prognostic biomarker in breast cancer.Entities:
Keywords: TGFβ; TGFβrIII; betaglycan; biomarker; breast cancer
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Year: 2015 PMID: 26190421 DOI: 10.3109/08977194.2015.1055740
Source DB: PubMed Journal: Growth Factors ISSN: 0897-7194 Impact factor: 2.511