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Updated: Jun 1, 2026

Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies
Published on: April 11, 2016
Optimizing targeted cancer therapy: towards clinical application of systems biology approaches
Arend H Sikkema1, Wilfred F A den Dunnen, Sander H Diks
1Beatrix Children's Hospital, Department of Pediatric Oncology, University Medical Center Groningen, University of Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands.
Abstract:
In cancer, genetic and epigenetic alterations ultimately culminate in discordant activation of signal transduction pathways driving the malignant process. Pharmacological or biological inhibition of such pathways holds significant promise with respect to devising rational therapy for cancer. Thus, technical concepts pursuing robust characterization of kinase activity in tissue samples from cancer patients have been subject of investigation. In the present review we provide a comprehensive overview of these techniques and discuss their advantages and disadvantages for systems biology approaches to identify kinase targets in oncological disease. Recent advances in the development and application of array-based peptide-substrate kinase activity screens show great promise in overcoming the discrepancy between the evaluation of aberrant cell signaling in specific malignancies or even individual patients and the currently available ensemble of highly specific targeted treatment strategies. These developments have the potential to result in a more effective selection of kinase inhibitors and thus optimize mechanism-based patient-specific therapeutic strategies. Given the results from current research on the tumor kinome, generating network views on aberrant tumor cell signaling is critical to meet this challenge.
Insights
This review highlights techniques for measuring kinase activity in cancer, aiding in the development of targeted therapies. Array-based screens offer promise for personalized cancer treatment strategies.
Area of Science:
- Oncology
- Molecular Biology
- Systems Biology
Background:
- Cancer arises from genetic and epigenetic alterations activating signal transduction pathways.
- Targeted inhibition of these pathways is a promising therapeutic strategy.
- Robust characterization of kinase activity in patient samples is crucial for identifying therapeutic targets.
Purpose of the Study:
- To provide a comprehensive overview of techniques for characterizing kinase activity in cancer.
- To discuss the advantages and disadvantages of these techniques for systems biology approaches.
- To highlight recent advances in array-based kinase activity screens for identifying oncological targets.
Main Methods:
- Review of existing technical concepts for kinase activity characterization.
- Discussion of array-based peptide-substrate kinase activity screening methods.
- Analysis of systems biology approaches for target identification.
Main Results:
- Various techniques exist for robust kinase activity characterization in cancer tissues.
- Array-based peptide-substrate kinase activity screens show significant promise.
- These screens can bridge the gap between aberrant signaling evaluation and targeted treatments.
Conclusions:
- Advances in kinase activity screening enable more effective selection of kinase inhibitors.
- Mechanism-based, patient-specific therapeutic strategies can be optimized.
- Network views of aberrant tumor cell signaling are critical for future cancer therapy development.
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