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      PAX8-PPARgamma1 fusion oncogene in human thyroid carcinoma [corrected].

      Science (New York, N.Y.)
      Adenocarcinoma, Follicular, genetics, metabolism, Adenoma, Adult, Aged, Carcinoma, Papillary, Cell Line, Cell Nucleus, Child, DNA-Binding Proteins, chemistry, pharmacology, physiology, Humans, Middle Aged, Nuclear Proteins, Oncogene Proteins, Fusion, Paired Box Transcription Factors, Receptors, Cytoplasmic and Nuclear, Response Elements, Thiazoles, Thiazolidinediones, Thyroid Neoplasms, Trans-Activators, Transcription Factors, Transcription, Genetic, Transcriptional Activation, Translocation, Genetic

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          Abstract

          Chromosomal translocations that encode fusion oncoproteins have been observed consistently in leukemias/lymphomas and sarcomas but not in carcinomas, the most common human cancers. Here, we report that t(2;3)(q13;p25), a translocation identified in a subset of human thyroid follicular carcinomas, results in fusion of the DNA binding domains of the thyroid transcription factor PAX8 to domains A to F of the peroxisome proliferator-activated receptor (PPAR) gamma1. PAX8-PPARgamma1 mRNA and protein were detected in 5 of 8 thyroid follicular carcinomas but not in 20 follicular adenomas, 10 papillary carcinomas, or 10 multinodular hyperplasias. PAX8-PPARgamma1 inhibited thiazolidinedione-induced transactivation by PPARgamma1 in a dominant negative manner. The experiments demonstrate an oncogenic role for PPARgamma and suggest that PAX8-PPARgamma1 may be useful in the diagnosis and treatment of thyroid carcinoma.

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