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Updated: May 19, 2026

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Published on: May 1, 2015
Receptor tyrosine kinases: principles and functions in glioma invasion
Mitsutoshi Nakada1, Daisuke Kita, Lei Teng
1Department of Neurosurgery, Division of Neuroscience, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, Ishikawa, 920-8640, Japan. mnakada@med.kanazawa-u.ac.jp
Abstract:
Protein tyrosine kinases are enzymes that are capable of adding a phosphate group to specific tyrosines on target proteins. A receptor tyrosine kinase (RTK) is a tyrosine kinase located at the cellular membrane and is activated by binding of a ligand via its extracellular domain. Protein phosphorylation by kinases is an important mechanism for communicating signals within a cell and regulating cellular activity; furthermore, this mechanism functions as an "on" or "off" switch in many cellular functions. Ninety unique tyrosine kinase genes, including 58 RTKs, were identified in the human genome; the products of these genes regulate cellular proliferation, survival, differentiation, function, and motility. Tyrosine kinases play a critical role in the development and progression of many types of cancer, in addition to their roles as key regulators of normal cellular processes. Recent studies have revealed that RTKs such as epidermal growth factor receptor (EGFR), platelet-derived growth factor receptor (PDGFR), c-Met, Tie, Axl, discoidin domain receptor 1 (DDR1), and erythropoietin-producing human hepatocellular carcinoma (Eph) play a major role in glioma invasion. Herein, we summarize recent advances in understanding the role of RTKs in glioma pathobiology, especially the invasive phenotype, and present the perspective that RTKs are a potential target of glioma therapy.
Insights
Receptor tyrosine kinases (RTKs) are crucial for cell signaling and cancer development. This review highlights RTK roles in glioma invasion, suggesting RTKs as potential therapeutic targets for brain tumors.
Area of Science:
- Biochemistry
- Molecular Biology
- Oncology
Background:
- Protein tyrosine kinases (PTKs) regulate cellular functions through phosphorylation.
- Receptor tyrosine kinases (RTKs) are cell surface enzymes activated by extracellular ligands.
- PTKs are vital for normal cellular processes, including proliferation and differentiation.
Purpose of the Study:
- To summarize recent findings on the role of RTKs in glioma pathobiology.
- To investigate the specific involvement of RTKs in the invasive phenotype of gliomas.
- To explore the potential of RTKs as therapeutic targets for glioma treatment.
Main Methods:
- Literature review of recent studies on RTKs and glioma.
- Analysis of the role of specific RTKs (e.g., EGFR, PDGFR, c-Met) in glioma invasion.
- Synthesis of current knowledge on RTK signaling pathways in glioma.
Main Results:
- RTKs are implicated in regulating normal cellular functions.
- Specific RTKs, including EGFR, PDGFR, c-Met, Tie, Axl, DDR1, and Eph, are significantly involved in glioma invasion.
- Dysregulation of RTK signaling contributes to glioma pathobiology and invasiveness.
Conclusions:
- RTKs play a critical role in the development and progression of various cancers, including gliomas.
- Understanding RTK involvement in glioma invasion is key to developing targeted therapies.
- RTKs represent a promising therapeutic avenue for combating glioma.
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