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Updated: Aug 16, 2026

Phosphopeptide Enrichment Coupled with Label-free Quantitative Mass Spectrometry to Investigate the Phosphoproteome in Prostate Cancer
Published on: August 2, 2018
Genetic analysis of the kinome and phosphatome in cancer
S Arena1, S Benvenuti, A Bardelli
1The Oncogenomics Center, Institute for Cancer Research and Treatment (IRCC), University of Torino Medical School, Candiolo, 10060, Italy.
Abstract:
Protein phosphorylation is a well-characterized biochemical process for reversible regulation of protein activity. Protein kinases and protein phosphatases are the key complementary players in this process, and through their coordinated activity cell homeostasis is tightly controlled. If these enzymes display aberrant activity, cells may undergo unrestrained growth, thus giving rise to complex diseases such as cancer. The technological platform gathered during the Human Genome Project recently allowed the systematic identification of the genetic alterations present in the kinase (the kinome) and the phosphatase (the phosphatome) gene families. These studies suggest that most if not all human tumors carry genetic alterations in at least one phosphatase or kinase gene. Here we integrate the biochemical knowledge on the properties of these molecules with the information collected through their systematic genetic analysis in cancer. We also analyze why the molecular profiling of the kinome and phosphatome in individual cancers is revolutionizing basic and clinical oncology.
Insights
Aberrant protein kinase (kinome) and phosphatase (phosphatome) activity drives cancer. Genetic analysis reveals most tumors have alterations in these enzyme families, revolutionizing cancer research and treatment.
Area of Science:
- Biochemistry and Molecular Biology
- Oncology
- Genetics
Background:
- Protein phosphorylation is a key regulatory mechanism for protein activity, essential for maintaining cell homeostasis.
- Protein kinases and phosphatases are critical enzymes involved in phosphorylation, with their coordinated action maintaining cellular balance.
- Dysregulation of these enzymes can lead to uncontrolled cell growth and diseases like cancer.
Purpose of the Study:
- To integrate biochemical knowledge of kinases and phosphatases with genetic alteration data in cancer.
- To analyze the impact of systematic genetic profiling of the kinome and phosphatome on cancer research.
- To understand how these insights are revolutionizing basic and clinical oncology.
Main Methods:
- Leveraging technological advancements from the Human Genome Project for systematic genetic analysis.
- Identifying genetic alterations within the kinome (kinase gene family) and phosphatome (phosphatase gene family).
- Integrating biochemical properties of these enzymes with their genetic alterations in cancer datasets.
Main Results:
- Systematic identification of genetic alterations in kinase and phosphatase gene families.
- Evidence suggests that the majority of human tumors harbor genetic alterations in at least one kinase or phosphatase gene.
- Molecular profiling of the kinome and phosphatome provides a new lens for understanding cancer biology.
Conclusions:
- Alterations in the kinome and phosphatome are prevalent in human cancers.
- Understanding these genetic changes is crucial for comprehending cancer development.
- The molecular profiling of kinases and phosphatases is transforming both basic and clinical oncology.
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