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GADD45B Transcript Is a Prognostic Marker in Papillary Thyroid Carcinoma Patients Treated With Total Thyroidectomy and Radioiodine Therapy

  • Mateus C. Barros-Filho*
  • , Julia B.H. de Mello
  • , Fabio A. Marchi
  • , Clóvis A.L. Pinto
  • , Igor C. da Silva
  • , Patricia K.F. Damasceno
  • , Milena B.P. Soares
  • , Luiz P. Kowalski
  • , Silvia R. Rogatto
  • *Kontaktforfatter
  • A.C.Camargo Cancer Center
  • Hospital São Rafael
  • Gonçalo Moniz Institute
  • SENAI CIMATEC

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

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Abstract

Currently, there is a lack of efficient recurrence prediction methods for papillary thyroid carcinoma (PTC). In this study, we enrolled 202 PTC patients submitted to total thyroidectomy and radioiodine therapy with long-term follow-up (median = 10.7 years). The patients were classified as having favorable clinical outcome (PTC-FCO, no disease in the follow-up) or recurrence (PTC-RE). Alterations in BRAF, RAS, RET, and TERT were investigated (n = 202) and the transcriptome of 48 PTC (>10 years of follow-up) samples was profiled. Although no mutation was associated with the recurrence risk, 68 genes were found as differentially expressed in PTC-RE compared to PTC-FCO. Pathway analysis highlighted a potential role of cancer-related pathways, including signal transduction and FoxO signaling. Among the eight selected genes evaluated by RT-qPCR, SLC2A4 and GADD45B showed down-expression exclusively in the PTC-FCO group compared to non-neoplastic tissues (NT). Increased expression of GADD45B was an independent marker of shorter disease-free survival [hazard ratio (HR) 2.9; 95% confidence interval (CI95) 1.2–7.0] in our cohort and with overall survival in the TCGA dataset (HR = 4.38, CI95 1.2–15.5). In conclusion, GADD45B transcript was identified as a novel prognostic marker candidate in PTC patients treated with total thyroidectomy and radioiodine therapy.

OriginalsprogEngelsk
Artikelnummer269
TidsskriftFrontiers in Endocrinology
Vol/bind11
Antal sider11
ISSN1664-2392
DOI
StatusUdgivet - 30. apr. 2020

Finansiering

Funding. This researched was funded by grants from the Funda??o de Amparo ? Pesquisa do Estado de S?o Paulo (FAPESP) (2015/17707-5 and 2015/20748-5).

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