Tyrosine Kinase Receptors in Oncology

Int J Mol Sci. 2020 Nov 12;21(22):8529. doi: 10.3390/ijms21228529.

Abstract

Tyrosine kinase receptors (TKR) comprise more than 60 molecules that play an essential role in the molecular pathways, leading to cell survival and differentiation. Consequently, genetic alterations of TKRs may lead to tumorigenesis and, therefore, cancer development. The discovery and improvement of tyrosine kinase inhibitors (TKI) against TKRs have entailed an important step in the knowledge-expansion of tumor physiopathology as well as an improvement in the cancer treatment based on molecular alterations over many tumor types. The purpose of this review is to provide a comprehensive review of the different families of TKRs and their role in the expansion of tumor cells and how TKIs can stop these pathways to tumorigenesis, in combination or not with other therapies. The increasing growth of this landscape is driving us to strengthen the development of precision oncology with clinical trials based on molecular-based therapy over a histology-based one, with promising preliminary results.

Keywords: research; tumorigenesis; tyrosine kinase receptor inhibitors; tyrosine kinase receptors.

Publication types

  • Review

MeSH terms

  • Anaplastic Lymphoma Kinase / metabolism
  • Carcinogenesis
  • ErbB Receptors / metabolism
  • Humans
  • Immunotherapy
  • Ligands
  • Neoplasms / metabolism*
  • Neovascularization, Pathologic
  • Phosphorylation
  • Precision Medicine
  • Protein-Tyrosine Kinases / metabolism
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-kit / metabolism
  • Receptor Protein-Tyrosine Kinases / antagonists & inhibitors*
  • Receptor Protein-Tyrosine Kinases / metabolism*
  • Receptor, ErbB-2 / metabolism
  • Receptor, Fibroblast Growth Factor, Type 1 / metabolism
  • Receptor, trkA / metabolism
  • Signal Transduction

Substances

  • Ligands
  • NTRK1 protein, human
  • Proto-Oncogene Proteins
  • ALK protein, human
  • Anaplastic Lymphoma Kinase
  • EGFR protein, human
  • ERBB2 protein, human
  • ErbB Receptors
  • FGFR1 protein, human
  • KIT protein, human
  • Protein-Tyrosine Kinases
  • Proto-Oncogene Proteins c-kit
  • ROS1 protein, human
  • Receptor Protein-Tyrosine Kinases
  • Receptor, ErbB-2
  • Receptor, Fibroblast Growth Factor, Type 1
  • Receptor, trkA