Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Preclinical models of LOXO-101 using TRK-fusion-bearing human-derived cancer cell lines demonstrate inhibition of the fusion oncoprotein and cellular proliferation in vitro, and tumor growth in vivo.
|
26216294 |
2015 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The following topics will be illustrated: (a) frequency of TRK oncogenes and correlation with radiation and tumor histopathological features; (b) molecular mechanisms underlying NTRK1 oncogenic rearrangements; (c) molecular and biochemical characterization of TRK oncoproteins, and their mechanism of action; (d) role of activating sequences in the activation of TRK oncoproteins.
|
19883730 |
2010 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Thus, our results show (1) that NPM-ALK and TPM3-ALK oncogenes are sufficient for lymphoma/leukemia development and required for tumor maintenance, hence validating ALK as potentially effective therapeutic target; and (2) for the first time, in vivo, the equal tumorigenic potential of the NPM-ALK and TPM3-ALK oncogenic tyrosine kinases.
|
20223922 |
2010 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In the context of astrocytomas, Trk receptors (TrkA, TrkB, TrkC) expression may promote tumor growth independently of grade.
|
17971243 |
2007 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Inflammatory myofibroblastic tumor with ALK/TPM3 fusion presenting as ileocolic intussusception: an unusual presentation of an unusual neoplasm.
|
16360423 |
2006 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Reciprocal NTRK1/TPM3 transcripts were found in 4 of 5 tumors with TPM3/NTRK1 re-arrangement, indicating an intra-chromosomal balanced reciprocal inversion.
|
10074915 |
1999 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Therefore, we have analyzed by different molecular approaches, including Southern blotting, DNA transfection assay on NIH-3T3 cells, and reverse transcription-PCR analysis, six papillary carcinomas from children living in the region of Belarus at the time of the Chernobyl nuclear accident to identify tumor-specific gene rearrangements of the proto-oncogenes RET and TRK, previously found activated in a tumor type-specific manner in papillary thyroid carcinoma.
|
7585643 |
1995 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Replacement of its extracellular domain by sequences coding for the 221 amino-terminal residues of the TPM3 gene was responsible for the oncogenic NTRK1 activation in three of eight of these tumors.
|
7590742 |
1995 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
TRK expression still had significant prognostic value when the analysis was restricted to tumors without N-myc amplification.
|
8441429 |
1993 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The same structural alterations of PTC and TRK (gene rearrangements) as well as of N-RAS (point mutation) detected in the NIH3T3 transformants, were also found in the original tumour DNAs, thus indicating that their activation was not due to transfection procedures.
|
2594368 |
1989 |