Targeting Selective Receptor Tyrosine Kinases in Refractory Embryonal Tumors of Childhood
Abstract
Embryonal tumors are a collection of biologically heterogeneous malignancies and the
exact cellular origin of these tumors is not known. Neuroblastoma (NB) and atypical
teratoid/rhabdoid tumor (AT/RT) are highly malignant tumors of embryonal origin that primarily affect infants and young children. Neuroblastoma is the most common type of extra cranial solid tumor in children. In the case of AT/RT, the survival rate of children affected by this disease is the lowest when compared to all embryonal tumors. Despite intensifying multimodal treatments, children affected with refractory AT/RT and NB have unacceptably high treatment failure and mortality rates.
To improve the clinical outcome of these malignancies, it is important to identify the key
molecules and cellular pathways responsible for tumor progression, survival and invasion. Many childhood cancers have high activation levels of selective receptor tyrosine kinase signaling pathways. Activation of these signaling pathways promotes cell proliferation, differentiation and cell survival. Therefore, receptor tyrosine kinases (RTKs) have become attractive therapeutic targets and the use of small molecule kinase inhibitors to block their signal transduction functions has led to the discovery of a number of novel therapeutics agents.
This research presents the relevant background information on two pediatric neoplasms
that we have selected to study and aims to provide the rationale for the development of useful new therapies for their treatment. Presented in details are the data with respect to the establishment of a screening approach to identify effective therapeutic agents with information on target validation and target modulation activities that can be utilized to design future clinical trials for these cancers.
Description
Keywords
Oncology
Citation
Singh, A. (2016). Targeting Selective Receptor Tyrosine Kinases in Refractory Embryonal Tumors of Childhood (Doctoral thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca. doi:10.11575/PRISM/27978