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Assessment of Resistance to Tyrosine Kinase Inhibitors by an Interrogation of Signal Transduction Pathways by Antibody Arrays
Published on: September 19, 2018
Small tyrosine kinase inhibitors as key molecules in the expression of metalloproteinases by solid tumors
Xanthi N Stahtea1, Olga Ch Kousidou, Andreas E Roussidis
1Department of Chemistry, Laboratory of Biochemistry, University of Patras, Patras, Greece.
Abstract:
Critical steps for cancer cell growth, migration, invasion, and metastasis are the interactions of extracellular matrix (ECM) molecules with cells, the disconnection of intercellular adhesion, and the degradation of ECM. The latter is mediated mainly by metalloproteinases (MMPs), the expression and activation of which is related to various tyrosine kinase receptors (RTKs). The aberrant RTK activity is associated with the development and progress of various human cancers. Tyrosine kinase inhibitors (TKIs) are small molecules which compete with ATP for binding to the kinase domain of the RTKs and have been used for the treatment of solid tumors. In this review, the recent advances of the effects of TKIs on MMPs expressed by solid tumors are presented.
Insights
Tyrosine kinase inhibitors (TKIs) impact matrix metalloproteinases (MMPs) in solid tumors. This review covers recent advances in understanding how TKIs affect MMPs, crucial for cancer metastasis.
Area of Science:
- Oncology
- Biochemistry
- Molecular Biology
Background:
- Cancer metastasis involves extracellular matrix (ECM) degradation, primarily mediated by matrix metalloproteinases (MMPs).
- MMP activity is linked to tyrosine kinase receptors (RTKs), whose aberrant activity drives cancer progression.
- Tyrosine kinase inhibitors (TKIs) target RTKs and are used in solid tumor treatment.
Purpose of the Study:
- To review recent advances in the effects of TKIs on MMPs in solid tumors.
- To highlight the relationship between RTK signaling and MMP expression in cancer.
Main Methods:
- Literature review of recent studies on TKIs and MMPs.
- Analysis of the molecular mechanisms linking RTKs, TKIs, and MMPs.
Main Results:
- TKIs modulate the expression and activity of various MMPs in solid tumors.
- The effects of TKIs on MMPs are diverse and depend on the specific TKI and tumor type.
- Understanding these interactions is key to optimizing TKI-based cancer therapies.
Conclusions:
- TKIs represent a promising therapeutic strategy by influencing MMPs involved in cancer metastasis.
- Further research is needed to fully elucidate the complex interplay between TKIs, RTKs, and MMPs for improved cancer treatment outcomes.
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