Neuroendocrine Tumors
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Changes in RET expression have been discovered in 30-70% of invasive breast cancers and 50-60% of pancreatic ductal adenocarcinomas in addition to colorectal adenocarcinoma, melanoma, small cell lung cancer, neuroblastoma, and small intestine neuroendocrine tumors.
|
31715421 |
2019 |
Neuroendocrine Tumors
|
0.100 |
Biomarker
|
group |
BEFREE |
In this review, we describe the current knowledge about the molecular mechanism of RET activation in human neuroendocrine tumors as well as the physiological roles and signal transduction of RET tyrosine kinase.
|
15013219 |
2004 |
Neuroendocrine Tumors
|
0.100 |
Biomarker
|
group |
BEFREE |
Medullary thyroid carcinoma (MTC) is a neuroendocrine tumor arising from "C" cells of the thyroid; it is a RET associated cancer that can be sporadic or familial in origin.
|
19887470 |
2009 |
Neuroendocrine Tumors
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Medullary thyroid carcinoma (MTC), a neuroendocrine tumor originating from thyroid parafollicular cells, has been demonstrated to be associated with mutations in RET, HRAS, KRAS and NRAS.
|
26718898 |
2016 |
Neuroendocrine Tumors
|
0.100 |
Biomarker
|
group |
BEFREE |
The RET gene encodes a tyrosine kinase receptor involved in different human neurocristopathies, such as specific neuroendocrine tumours and Hirschsprung disease (HSCR).
|
12865274 |
2003 |
Neuroendocrine Tumors
|
0.100 |
GeneticVariation
|
group |
BEFREE |
No mutations were identified in RET exons 10, 11, and 13-16, regions previously implicated in SCLC or other neuroendocrine tumors.
|
9559344 |
1998 |
Neuroendocrine Tumors
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Therefore, the genes encoding both GDNF and GDNFR-alpha are excellent candidates for a role in the pathogenesis of those MEN 2 families and sporadic neuroendocrine tumors without RET mutations.
|
9284737 |
1997 |
Neuroendocrine Tumors
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Although the numbers of each investigated neuroendocrine tumor type are small, our data indicate that oncogenic RET proto-oncogene mutations are involved in the formation of a subset of sporadically occurring medullary thyroid carcinomas and pheochromocytomas but do not appear to be generally important in the formation of other types of sporadically occurring neuroendocrine tumors.
|
8964826 |
1996 |
Neuroendocrine Tumors
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Paragangliomas are neuroendocrine tumors frequently associated with mutations in RET, NF1, VHL, and succinate dehydrogenase (SDHx) genes.
|
23707781 |
2013 |
Neuroendocrine Tumors
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Point mutations in neuroendocrine neoplasm-related genes like RB1 or RET were not detected, but one tumor harbored a heterozygous RB1 deletion.
|
28059096 |
2017 |
Neuroendocrine Tumors
|
0.100 |
Biomarker
|
group |
BEFREE |
In this review, we summarize progress in the study of RET from bench to bedside, focusing on pathophysiology of neuroendocrine tumors.
|
17036197 |
2006 |
Neuroendocrine Tumors
|
0.100 |
GeneticVariation
|
group |
BEFREE |
RET mutations play an important role in the development of human neuroendocrine tumors.
|
19411807 |
2009 |