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Orientador(es)
Resumo(s)
Peroxisome proliferator-activated receptor gamma (PPAR gamma) gene is a nuclear receptor that is involved in thyroid tumourigenesis. Recently, our group has shown that follicular carcinomas underexpressing PPAR gamma protein are more prone to develop distant metastases, to invade locally, to present poorly differentiated areas and to persist after surgery. Aneuploidy is also observed in some thyroid tumours, particularly in the more advanced cases. The aim of the present study was to investigate the association of PPAR gamma expression with the degree of differentiation and ploidy status of benign and malignant thyroid neoplasias. DNA cytometric studies, ploidy and S-phase fraction (SPF) determination, and quantitative RT-PCR analysis of molecular markers specific for thyroid follicular cells, namely Tg (thyroglobulin), TSHR (TSH receptor) and NIS (Na+/I- symporter) were compared between thyroid lesions with positive or negative PPAR gamma protein expression. We observed that PPAR gamma-negative tissues expressed lower levels of Tg mRNA [4.66x10(6) a.u. (arbitrary units) +/- 1.49x10(6)], and were more frequently aneuploid (36%), and presented higher SPF (3.1%+/- 0.4) than PPAR gamma-positive samples (Tg mRNA = 2.54x10(7) a.u. +/- 9.72 x 10(6). P=0.0006; aneuploidy=8%, P=0.0031; SPF=2.2%+/- 0.2, P=0.0430). A similar trend was also observed for TSHR and NIS mRNA, although not reaching statistical significance. This study showed that underexpression of PPAR gamma is associated with poor tumour differentiation, aneuploidy and higher cell proliferative activity. Therapies designed to modulate expression of PPAR gamma may have an impact on the growth of thyroid neoplasias.
Descrição
Funding: This study was supported by Fundação para a Ciência e Tecnologia (POCTI/CBO/48922/2002), Portugal.
Palavras-chave
Ni+/I-symporterACTIVATED RECEPTOR-GAMMA TSH receptor FLOW-CYTOMETRY GROWTH-INHIBITION thyroglobulin PPAR gamma aneuploidy DNA-BINDING ACTIVITY thyroid GENE-EXPRESSION HUMAN BREAST-CANCER INDUCE APOPTOSIS HUMAN COLON-CANCER TERMINAL DIFFERENTIATION CARCINOMA-CELLS
