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High-risk cancers could be identified sooner after major prostate cancer study

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Health Desk

In Short: Scientists have identified eight genetic 'footprints' that explain 85% of prostate cancers, potentially enabling earlier detection and personalized treatment.

Barriers to conducting replications of experiment in cancer research
Photo: Authors of the study: Timothy M Errington, Alexandria Denis, Nicole Perfito, Elizabeth Iorns, Brian A Nosek / Wikimedia Commons (CC BY 4.0)

In a new study published in the journal Nature, researchers from the Pan Prostate Cancer Group (PPCG) have uncovered genetic 'footprints' that could help identify which prostate cancers are most likely to become aggressive. This breakthrough, which accounts for approximately 85% of prostate cancers, could lead to earlier detection and personalized treatment options.

The study, involving 959 men, evaluated tumor tissue samples and found that four of the 'integrated mutational footprints' were associated with aggressive tumors more prone to spreading outside the prostate. Experts believe these findings could pave the way for superior screening tests and earlier identification of high-risk cancers.

Professor Ros Eeles, from the Institute of Cancer Research (ICR) and The Royal Marsden NHS Foundation Trust, said, 'For many years we’ve known that prostate cancer is not a single disease. This research provides important new clues regarding the biological mechanisms driving the illness, which could lead to better screening tests and earlier identification of high-risk cancers.

The next step for the research team is to use these findings to develop and test classification systems for prostate cancer tumors using molecular information. This could help identify aggressive cancers sooner and guide personalized treatment decisions, potentially saving lives.

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