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Updated: Jul 19, 2026

Impedance-based Real-time Measurement of Cancer Cell Migration and Invasion
Published on: April 2, 2020
Focal adhesion kinase: a potential target in cancer therapy
Maroesja J van Nimwegen1, Bob van de Water
1Division of Toxicology, Leiden/Amsterdam Center for Drug Research, Leiden University, Gorlaeus Laboratories, 2300 RA Leiden, The Netherlands.
Abstract:
Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase that plays an important role in signal transduction pathways that are initiated at sites of integrin-mediated cell adhesions and by growth factor receptors. FAK is a key regulator of survival, proliferation, migration and invasion: processes that are all involved in the development and progression of cancer. FAK is also linked to oncogenes at both a biochemical and functional level. Moreover, overexpression and/or increased activity of FAK is common in a wide variety of human cancers, implicating a role for FAK in carcinogenesis. Given the important role of FAK in a large number of processes involved in tumorigenesis, metastasis and survival signalling FAK should be regarded as a potential target in the development of anti-cancer drugs. Therefore, selective inhibitors of FAK need to be developed. Combination of these selective FAK inhibitors with cytotoxic agents could be a very promising anti-cancer therapy.
Insights
Focal adhesion kinase (FAK) is crucial for cancer progression. Developing selective FAK inhibitors, potentially combined with cytotoxic agents, offers a promising anti-cancer therapy strategy.
Area of Science:
- Molecular biology
- Oncology
- Biochemistry
Background:
- Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase involved in integrin and growth factor receptor signaling.
- FAK regulates critical cellular processes including survival, proliferation, migration, and invasion, all implicated in cancer development and progression.
- Overexpression and/or increased activity of FAK is frequently observed in various human cancers, suggesting its role in carcinogenesis.
Purpose of the Study:
- To highlight the significant role of FAK in tumorigenesis, metastasis, and survival signaling.
- To propose FAK as a potential therapeutic target for anti-cancer drug development.
- To advocate for the development of selective FAK inhibitors.
Main Methods:
- Review of existing literature on FAK's role in cell signaling and cancer.
- Analysis of FAK's biochemical and functional links to oncogenes.
- Evaluation of FAK's prevalence and activity in human cancers.
Main Results:
- FAK is a key regulator of cellular processes vital for cancer progression.
- FAK is biochemically and functionally linked to oncogenes.
- Elevated FAK levels and activity are common across many human cancers.
Conclusions:
- FAK is a critical factor in tumor development, metastasis, and survival.
- Selective FAK inhibitors should be developed as a targeted anti-cancer therapy.
- Combining FAK inhibitors with cytotoxic agents presents a promising therapeutic approach.
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