AI Article Synopsis

  • Type III transforming growth factor (TGFβ) receptor (TGFβrIII) is found to be downregulated in breast cancer tissues, which is significant for understanding tumor signaling.
  • In a study of 47 breast cancer patients and 36 healthy women, lower levels of soluble TGFβrIII (sTGFβrIII) were identified in patients, effectively distinguishing between cancer and health with high accuracy.
  • Higher pre-surgery levels of sTGFβrIII correlated with improved progression-free survival, while levels rose after surgery, indicating its potential as a useful biomarker for diagnosis and prognosis in breast cancer.

Article 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.

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Source
http://dx.doi.org/10.3109/08977194.2015.1055740DOI Listing

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