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RORγt may Influence the Microenvironment of Thyroid Cancer Predicting Favorable Prognosis.
Cunha, Lucas Leite; Morari, Elaine Cristina; Nonogaki, Suely; Bufalo, Natassia Elena; da Assumpção, Ligia Vera Montalli; Soares, Fernando Augusto; Vassallo, José; Ward, Laura Sterian.
Affiliation
  • Cunha LL; Laboratory of Cancer Molecular Genetics, Faculty of Medical Sciences, University of Campinas (Unicamp), Campinas, Brazil.
  • Morari EC; Laboratory of Cancer Molecular Genetics, Faculty of Medical Sciences, University of Campinas (Unicamp), Campinas, Brazil.
  • Nonogaki S; Department of Biological and Health Sciences, State University of Roraima, Boa Vista, Brazil.
  • Bufalo NE; Adolfo Lutz Institute, São Paulo, Brazil.
  • da Assumpção LVM; Laboratory of Cancer Molecular Genetics, Faculty of Medical Sciences, University of Campinas (Unicamp), Campinas, Brazil.
  • Soares FA; Laboratory of Cancer Molecular Genetics, Faculty of Medical Sciences, University of Campinas (Unicamp), Campinas, Brazil.
  • Vassallo J; Department of General Pathology, Dental School, University of São Paulo, São Paulo, Brazil.
  • Ward LS; Pathology Division, ID'Or Research Institute, Rede D'Or Hospitals Network, São Paulo, Brazil.
Sci Rep ; 10(1): 4142, 2020 03 05.
Article in En | MEDLINE | ID: mdl-32139737
ABSTRACT
We aimed to investigate the role of RORγt (Retinoic acid-related orphan receptor gamma) in the tumor microenvironment of differentiated thyroid carcinoma. We retrospectively analyzed 56 patients (48 papillary and 8 follicular thyroid carcinomas). Immunohistochemical expression of RORγt was compared to other immune markers previously investigated by our group, clinical and pathological information. All patients presented cytoplasmic expression of RORγt in thyroid tumor cells. Seven (12.5%) patients presented no nuclear expression of RORγt. Positivity was few (up to 10%) in 14 patients; 10 to 50% in 5 patients (8.9%); and more than 50% in 30 patients (53.6%). Nuclear RORγt positivity was associated with absence of distant metastasis at diagnosis (p = 0.013) and the need of less cumulative doses of radioactive iodine (p = 0.039). Patients whose tumors were positive for nuclear RORγt presented higher 10-years relapse-free survival rate than those patients who were negative for RORγt (p = 0.023). We classified the patients according to the clustering of immunological immunohistochemical markers. We were able to distinguish a subset (A) of 38 patients who presented high expression of nuclear RORγt and tended to be scarce in proinflammatory immune markers. Other 16 patients integrated a second subset (B) whose tumor microenvironment accumulated proinflammatory markers and presented low expression of nuclear nuclear RORγt. Distant metastasis at diagnosis were more frequent among patients from cluster B than from cluster A (p = 0.008). Our results reinforce that the expression of RORγt together with other immune markers might help predict the prognosis of patients with thyroid cancer and help individualize clinical management.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thyroid Neoplasms / Nuclear Receptor Subfamily 1, Group F, Member 3 Type of study: Observational_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Sci Rep Year: 2020 Document type: Article Affiliation country: Brazil

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thyroid Neoplasms / Nuclear Receptor Subfamily 1, Group F, Member 3 Type of study: Observational_studies / Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Sci Rep Year: 2020 Document type: Article Affiliation country: Brazil