RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease BEFREE It was originally identified in chimeric genes caused by chromosomal translocation involving RET proto-oncogene in some thyroid tumors. 30909182 2019
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease BEFREE The relatively low prevalence of RET activation in PDCs argues against a major role for RET/PTC in the progression from well to poorly differentiated thyroid tumor phenotypes. 11788678 2002
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE Nevertheless, an extensive molecular analysis that included all codons was prompted by the diagnosis of thyroid neoplasm in a patient's sister, and identified the rare intracellular RET p.Ser891Ala mutation. 23295303 2012
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease LHGDN These results suggest that, if the association between HT and thyroid cancer exists, its molecular basis is different from RET/PTC rearrangement. 11927965 2002
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE Since fine-needle aspiration biopsy (FNAB) is an important component of the preoperative management of patients with thyroid tumors, we developed a rapid (20-min) method that enables extraction of DNA from FNABs for RET mutation analysis. 9824378 1998
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease BEFREE Analysis by a reverse transcriptase-polymerase chain reaction method showed that the ret rearrangement-positive tumor contained the PTC/retTPC chimeric transcript, which was reported to be found specifically in thyroid tumors and adenomatous goiter. 1381340 1992
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE Rearrangements of the RET receptor tyrosine kinase gene generating RET/PTC oncogenes are specific to papillary thyroid carcinoma (PTC), the most frequent thyroid tumor. 16203990 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE Here we describe the first evidence of ret proto-oncogene rearrangement of thyroid cancer tissues around the site. 10551507 1999
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease LHGDN A new germline point mutation in Ret exon 8 (cys515ser) in a family with medullary thyroid carcinoma. 18631007 2008
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease BEFREE We did a comprehensive screen for 548 known and putative fusion genes in 27 samples of thyroid tumors and three positive controls-one thyroid cancer cell line (TPC-1) and two PTCs with known CCDC6-RET (alias RET/PTC1) fusion gene, using this microarray. 22961909 2012
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE A G691S RET polymorphism was present with a higher frequency in radiation-induced epithelial thyroid tumours (55%) than in sporadic tumours (20%) and in control normal thyroid tissues (15%). 12085189 2002
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE The catalytic domain of RET can be used also for X-ray diffraction to obtain information about the three-dimensional structure, necessary for a rational design of selective inhibitors: it represents an important tool to understand the molecular mechanisms causing thyroid cancer and to care it. 16490247 2006
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease LHGDN The RET IVS1-126G>T variant is strongly associated with the development of sporadic medullary thyroid cancer. 15142370 2004
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease LHGDN In conclusion, we found RET amplification, which is a rare oncogenic aberration, in thyroid cancer. 17270245 2007
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 AlteredExpression disease BEFREE ZD 6474 has shown promising activity in preclinical models against RET kinase, and its contemporary inhibition of vascular endothelial growth factor and epidermal growth factor pathways renders it a very attractive drug for clinical trials in thyroid cancer. 16940797 2006
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease BEFREE Several types of rearrangement known to occur in thyroid cancer, including RET/PTC, NTRK1 and BRAF/AKAP9, are more common in radiation-associated thyroid tumors and RET/PTC can be induced experimentally by exposing human thyroid cells to ionizing radiation. 19766698 2010
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE Germline RET proto-oncogene mutations are the genetic causes of multiple endocrine neoplasia type 2 and a strong genotype-phenotype correlation exists, particularly between a specific RET codon mutation and the (a) age-related onset and (b) thyroid tumor progression, from C-cell hyperplasia to medullary thyroid carcinoma and, ultimately, to nodal metastases. 22584703 2012
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease BEFREE The discovery of the RET proto-oncogene and its role in tumorigenesis have improved our understanding of thyroid cancer. 11069217 2001
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease BEFREE Using human thyroid cancer-derived cell lines [harboring rearranged during transfection (RET)/PTC, v-RAF murine sarcoma viral oncogene homolog B (BRAF), or rat sarcoma virus oncogene (RAS) alterations], we determined that IL-6/gp130/JAK signaling is responsible for STAT3 activation. 22891351 2012
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE Medullary thyroid carcinomas (MTC) derive from C cells in the thyroid and express some specific messenger RNAs (mRNA), such as those transcribed from the RET proto-oncogene, the calcitonin gene, and the gene for carcinoembryonic antigen (CEA), which usually do not exist in normal thyroid follicular cells or thyroid tumors of follicular epithelial descent. 10084577 1999
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE Specific genetic lesions are associated to each thyroid tumor histotype: BRAF mutations and RET/PTC and TRK oncogenes have been detected in PTC, whereas FTC is characterized by PAX8/PPARgamma rearrangements and RAS mutations. 19910897 2009
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease LHGDN Alternative mutations of BRAF, RET and NTRK1 are associated with similar but distinct gene expression patterns in papillary thyroid cancer. 15273715 2004
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE Somatic rearrangements of RET are involved in the aetiology of a variable proportion of papillary thyroid carcinomas (PTC), the most common type of thyroid tumour whose prevalence is increasing in areas heavily exposed to radioactive fallout after the Chernobyl accident of 1986. 8901418 1996
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease LHGDN Here, we show that nuclear localization of beta-catenin is frequent in both thyroid tumors and their metastases from MEN 2 patients, suggesting a novel mechanism of RET-mediated function through the beta-catenin signaling pathway. 18316596 2008
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease LHGDN Familial medullary thyroid carcinoma: clinical variability and low aggressiveness associated with RET mutation at codon 804. 11932300 2002