Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 Biomarker disease BEFREE Taken together, these results suggest that PPARgamma agonist inhibit cell growth of some types of human thyroid cancer. 11344222 2001
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 GeneticVariation disease BEFREE The absence of PAX8-PPARgamma rearrangements in Hurthle cell tumors and papillary thyroid carcinomas highlights the differences in the molecular pathogenesis of these thyroid tumors. 12170088 2002
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 GeneticVariation disease BEFREE Involvement of the PAX8/peroxisome proliferator-activated receptor gamma rearrangement in follicular thyroid tumors. 12970322 2003
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 Biomarker disease BEFREE The purpose of this study was to evaluate the possibility for the therapeutic effect of PPARgamma ligands against anaplastic thyroid tumor in vitro. 14654945 2004
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 Biomarker disease BEFREE The objectives of the present work were: to study and compare the relative expression of PPARgamma in normal, benign and malignant thyroid tissues and to correlate PPARgamma immunostaining with clinical/pathological features of patients with thyroid cancer. 15238980 2004
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 AlteredExpression disease LHGDN Retinoid X receptor-gamma and peroxisome proliferator-activated receptor-gamma expression predicts thyroid carcinoma cell response to retinoid and thiazolidinedione treatment. 15299084 2004
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 Biomarker disease BEFREE Genetic alterations involving the thyroid transcription factor PAX8 and the peroxisome proliferator-activated receptor gamma 1 (PPARgamma1) genes have been described in thyroid neoplasms. 15362967 2004
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 Therapeutic disease CTD_human Our investigations document that human thyroid cancer cell lines commonly express PPARgamma, but chromosomal translocations involving PPARgamma are uncommon. 15785241 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 AlteredExpression disease BEFREE Our investigations document that human thyroid cancer cell lines commonly express PPARgamma, but chromosomal translocations involving PPARgamma are uncommon. 15785241 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 Biomarker disease LHGDN Our investigations document that human thyroid cancer cell lines commonly express PPARgamma, but chromosomal translocations involving PPARgamma are uncommon. 15785241 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 GeneticVariation disease LHGDN PAX8-PPARgamma rearrangement is frequently detected in the follicular variant of papillary thyroid carcinoma. 16219715 2006
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 Biomarker disease BEFREE Rosiglitazone is a peroxisome proliferator-activated receptor gamma (PPARgamma) agonist that has been shown to induce differentiation, cell cycle arrest, and apoptosis in a variety of human cancers including thyroid cancer. 17188145 2006
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 Biomarker disease LHGDN The Ras effector NORE1A is suppressed in follicular thyroid carcinomas with a PAX8-PPARgamma fusion. 16352687 2006
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 Biomarker disease BEFREE Using this mutant mouse, we tested the hypothesis that the peroxisome proliferator-activated receptor gamma (PPARgamma) could function as a tumor suppressor in thyroid cancer in vivo. 16314832 2006
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 GeneticVariation disease LHGDN Here, we report our discovery of a novel CREB3L2-PPARgamma fusion mutation in thyroid carcinoma with t(3;7)(p25;q34), showing that a family of somatic PPARgamma fusion mutations exist in thyroid cancer. 18757431 2008
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 GeneticVariation disease BEFREE As such, this article addresses the following aspects of intragenic mutations in thyroid cancer: thyroid stimulating hormone receptor and guanine-nucleotide-binding proteins of the stimulatory family mutations in hyperfunctioning tumors; mutations in RAS and other genes and aneuploidy; PAX8-PPARgamma rearrangements; BRAF mutations; mutations in oxidative phosphorylation and Krebs cycle genes in Hürthle cell tumors; mutations in succinate dehydrogenase genes in medullary carcinoma and C-cell hyperplasia; and mutations in TP53 and other genes in poorly differentiated and anaplastic carcinomas. 18502330 2008
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 GeneticVariation disease BEFREE The common somatic genetic changes in thyroid cancer of follicular cell origin (RET/PTC, NTRK, RAS, BRAF, PAX8-PPARgamma) are generally mutually exclusive, with distinct genotype-histologic subtype of thyroid cancer and genotype-phenotype associations observed. 18043251 2008
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 Biomarker disease LHGDN Peroxisome proliferator-activated receptor gamma inhibits follicular and anaplastic thyroid carcinoma cells growth by upregulating p21Cip1/WAF1 gene in a Sp1-dependent manner. 18509005 2008
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 GeneticVariation disease BEFREE Here, we report our discovery of a novel CREB3L2-PPARgamma fusion mutation in thyroid carcinoma with t(3;7)(p25;q34), showing that a family of somatic PPARgamma fusion mutations exist in thyroid cancer. 18757431 2008
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 GeneticVariation disease BEFREE The molecular pathology of thyroid cancer is now better understood because of our ability to identify RET/PTC rearrangements and BRAF mutations in the aetiopathogenesis of the large majority of PTCs and the high prevalence of RAS mutations and PAX8/PPARgamma rearrangements in follicular patterned carcinomas (FTCs and follicular variant of PTCs). 19147628 2009
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 Biomarker disease BEFREE Underexpression of PPARgamma is associated with aneuploidy and lower differentiation of thyroid tumours of follicular origin. 19724872 2009
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 GeneticVariation disease BEFREE In this study, a group of 60 follicular thyroid neoplasms [18 FTC, 1 Hurthle cell carcinoma (HCC), 24 follicular thyroid adenomas (FTA), 5 Hurthle cell adenomas (HCA), and 12 follicular variants of papillary thyroid carcinomas (FV-PTC)] were analyzed to determine the prevalence of the PAX8-PPARG translocation by fluorescence in situ hybridization. 19963130 2010
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 GeneticVariation disease BEFREE Common mutations found in thyroid cancer are point mutation of the BRAF and RAS genes as well as RET/PTC and PAX8/PPARγ chromosomal rearrangements. 21878896 2011
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 Biomarker disease BEFREE The aim of the present study was to develop a method for the detection of chimeric PAX8-PPARG transcripts in formalin-fixed paraffin-embedded (FFPE) thyroid tumor samples by conventional RT-PCR. 22179975 2012
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.400 Biomarker disease BEFREE TSH receptor mRNA reverse transcription-polymerase chain reaction, the Veracyte and Asuragen commercial methods, and the noncommercial use of BRAF, RAS, RET/PTC, and PAX8/PPARγ testing have promising roles in the diagnosis and treatment of patients with nodular thyroid disease and thyroid cancer. 22984796 2013