Completed Cancer Diabetes, Hormones & Metabolism

Investigation of the role of metabolism in tumorigenesis

In plain English

AI plain-English summary

Cancer cells are voracious consumers of glucose and glutamine, but scientists still do not fully understand whether this metabolic hunger itself helps trigger the disease, or is merely a symptom of genetic mutations. Most cancer research focuses on faulty genes. This programme shifts attention to the fuel supply: the metabolic pathways that cancer cells depend on to grow. The team will systematically switch off metabolic genes in cell cultures and animal models to see which ones actually drive tumour formation. They want to know not just *that* metabolism matters, but *how* specific metabolic changes push a normal cell toward cancer. If the work succeeds, it could reveal new drug targets—molecules that healthy cells need less urgently than cancer cells do, making them safer to attack. The researchers also plan to detect early metabolic changes in urine and blood, which could lead to simple, non-invasive screening tests that catch cancers long before symptoms appear. This is fundamental science. The immediate output will be a clearer map of the metabolic wiring that enables tumour growth. That map will not cure cancer tomorrow, but it will tell drug developers and diagnostic engineers exactly where to look.

View original technical description
Cancer is currently viewed as a genetic disease whereby well-characterised gene mutations are sufficient to drive unrestrained growth and proliferation. In order to support proliferation, cancer cells utilise a specific set of nutrients, among which glucose and glutamine are the most important. It has been shown that inherent dysfunctions of glucose and glutamine metabolism in some circumstances predispose to cancer formation. However, how altered metabolism drives tumorigenesis in not fully understood. In this programme, we intend to investigate the role of metabolic genes involved in cancer formation using cell culture and animal models. Our goal is to define how each candidate gene triggers tumorigenesis in vivo and to find metabolic pathways required for the survival of these mutant tumours in order to determine potential anti-cancer drug targets. Furthermore, we aim to detect early signs of these metabolic changes in body fluids such as urine and blood, in order to discover novel biomarkers for the early detection of cancer.

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Researchers

Christian Frezza (Principal Investigator)Rebecca Fitzgerald (Co-Investigator)

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Original classification

Intramural

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