AI Article Synopsis

  • Medullary thyroid carcinoma (MTC) represents about 5% of thyroid cancers, and while surgery is the main treatment, advanced cases don't respond well to traditional chemotherapy, highlighting the need for new treatment targets.
  • This study involved 79 patients with MTC to analyze the connection between certain proteins (survivin and XIAP) and clinical outcomes, using tissue samples to explore their roles in disease progression and survival rates.
  • Findings revealed that higher levels of survivin and XIAP were linked to more advanced disease stages and poorer patient survival, suggesting that these proteins could be potential targets for new therapies in MTC.

Article Abstract

Background: Medullary thyroid carcinoma (MTC) accounts for ∼5% of all thyroid malignancies. To date, surgery is the first-line therapy with curative intention. However, for advanced MTC, conventional chemotherapeutic agents do not provide convincing results. Therefore, the identification of biomarkers that can be antagonised by small-molecule therapeutics may lead to novel encouraging treatment options.

Methods: Seventy-nine patients with surgically resected and histologically confirmed MTC were included in this study. Tissue microarrays were constructed to assess the relationship between inhibitor of apoptosis proteins (IAPs) survivin or XIAP expression levels and clinicopathological variables as well as overall survival.

Results: High survivin or XIAP expression was associated with an advanced T-stage and metastatic disease. Whereas tissue expression levels of survivin correlated with serum calcitonin levels, XIAP was overexpressed in the subgroup of patients with sporadic MTC. Both IAPs were negatively associated with patient survival in the multivariate Cox regressions analysis (survivin: hazard ratio (HR) 1.62; 95% confidence interval (CI): 1.21-2.16; P=0.001; XIAP: HR 1.78; 95% CI: 1.16-2.72; P=0.008).

Conclusions: Survivin and XIAP demonstrate distinct expression patterns in MTCs, which are associated with advanced disease and poor prognosis. We thus provide first evidence that both IAPs might serve as viable targets in patients with MTC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4815780PMC
http://dx.doi.org/10.1038/bjc.2016.5DOI Listing

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