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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
Thyroid Neoplasm
|
0.700 |
Biomarker
|
disease |
LHGDN |
In conclusion, we found RET amplification, which is a rare oncogenic aberration, in thyroid cancer.
|
17270245 |
2007 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |