[HTML][HTML] Detection of tumor NTRK gene fusions to identify patients who may benefit from tyrosine kinase (TRK) inhibitor therapy

SJ Hsiao, A Zehir, AN Sireci, DL Aisner - The Journal of Molecular …, 2019 - Elsevier
Chromosomal rearrangements involving the NTRK1, NTRK2, and NTRK3 genes (NTRK
genes), which encode the high-affinity nerve growth factor receptor (TRKA), brain-derived …

TrkB truncated isoform receptors as transducers and determinants of BDNF functions

L Tessarollo, S Yanpallewar - Frontiers in Neuroscience, 2022 - frontiersin.org
Brain-derived neurotrophic factor (BDNF) belongs to the neurotrophin family of secreted
growth factors and binds with high affinity to the TrkB tyrosine kinase receptors. BDNF is a …

Systematic review of the receptor tyrosine kinase superfamily in neuroblastoma pathophysiology

EJ Rozen, JM Shohet - Cancer and Metastasis Reviews, 2022 - Springer
Background Neuroblastoma is a devastating disease accounting for 15% of all childhood
cancer deaths. Yet, our understanding of key molecular drivers such as receptor tyrosine …

Targeting TRK: A fast-tracked application of precision oncology and future directions

A Kojadinovic, B Laderian, PS Mundi - Critical Reviews in Oncology …, 2021 - Elsevier
The NTRK genes encode the tropomyosin-related receptor tyrosine kinases TrkA, TrkB and
TrkC. TRK receptors regulate the proliferation, differentiation, and survival of many neuronal …

ING5 activity in self-renewal of glioblastoma stem cells via calcium and follicle stimulating hormone pathways

F Wang, AY Wang, C Chesnelong, Y Yang, A Nabbi… - Oncogene, 2018 - nature.com
Stem cell-like brain tumor initiating cells (BTICs) cause recurrence of glioblastomas, with
BTIC 'stemness' affected by epigenetic mechanisms. The ING family of epigenetic regulators …

Genetic etiology study in a large cohort with congenital insensitivity to pain with anhidrosis

S Li, X Ren, Y Guan, F Zhao, Y Cao, X Geng, Y Wang… - Pain, 2024 - journals.lww.com
Pathogenic variations in the NTRK1 can cause congenital insensitivity to pain with
anhidrosis (CIPA), a rare autosomal recessive inherited neuropathy. The precise diagnosis …

Nuclear receptor tyrosine kinase transport and functions in cancer

MK Chen, JL Hsu, MC Hung - Advances in Cancer Research, 2020 - Elsevier
Signaling functions of plasma membrane-localized receptor tyrosine kinases (RTKs) have
been extensively studied after they were first described in the mid-1980s. Plasma membrane …

Novel NTRK1 mutations in Chinese patients with congenital insensitivity to pain with anhidrosis

X Geng, Y Liu, XZ Ren, Y Guan, Y Wang… - Molecular …, 2018 - journals.sagepub.com
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive
disorder, characterized by loss of algesthesis and inability to sweat. CIPA is known to be …

Structural analysis of TrkA mutations in patients with congenital insensitivity to pain reveals PLCγ as an analgesic drug target

BC Moraes, HV Ribeiro-Filho, AP Roldão… - Science …, 2022 - science.org
Chronic pain is a major health issue, and the search for new analgesics has become
increasingly important because of the addictive properties and unwanted side effects of …

The oncogenic neurotrophin receptor tropomyosin-related kinase variant, TrkAIII

AR Farina, L Cappabianca, P Ruggeri, L Gneo… - Journal of Experimental …, 2018 - Springer
Oncogenes derived from the neurotrophin receptor tropomyosin-related kinase TrkA act as
drivers in sub-populations of a wide-range of human cancers. This, combined with a recent …