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Cancer-causing gene regulates genetic variation in prostate cancer: Research

by Medically Speaking Team

Researchers from the Barts Cancer Institute (BCI) at Queen Mary University of London, the Italian Institute for Genomic Medicine, and the University of Milan discovered a novel role for a cancer-causing gene in controlling an important genetic process that underpins genetic variation in prostate cancer.

The findings, published today in Cell Reports, reveal how the gene influences the generation of genetic variants in prostate cancer that may predict disease relapse and represent new drug targets to improve patient survival. Co-senior author Dr Prabhakar Rajan, Group Leader at BCI and Consultant Urological Surgeon at Barts Health NHS Trust, said: “Prostate cancer is the commonest male cancer in the world and lead cause of male cancer-related death. It is very variable in its genetic makeup, which makes diagnosis and treatment tricky, as there is not a one size fits all approach for treating patients. A knowledge of the drivers of genetic variability will help us understand the disease better, and improve treatments.”

Alternative splicing is the process of rearranging gene segments to generate distinct combinations of genetic information known as’splice variants,’ which include the instructions for making proteins. A single gene can code for numerous proteins that are produced at different levels and serve distinct roles in the cell thanks to alternative splicing.

Alternative splicing is a critical mechanism in normal cells for regulating gene expression and producing genetic and protein variety; nevertheless, it is disturbed in many cancer types, including prostate cancer.

The researchers discovered that the cancer-causing gene FOXA1 is a critical regulator of alternative splicing in prostate cancer and may affect the formation of splice variants that influence disease recurrence and patient survival in this study.

FOXA1 fine-tunes alternative splicing in prostate cancer

FOXA1 is a type of protein known as a pioneer transcription factor. Transcription factors can select which genes in DNA are transcribed into the instructions used to make proteins within our cells and the rate at which this occurs. As a pioneer factor, FOXA1 opens up DNA for binding by distinct transcription factors. Changes to FOXA1 have been found to drive the initiation and progression of prostate cancer.

By assessing alternative splicing in cell line models and primary cases of prostate cancer, the team found that high levels of FOXA1 limited genetic diversity towards splice variants that have a functional benefit for the cancer cells. The investigations revealed that FOXA1 favoured splice variants that were present at high levels within the cells and silenced splice variants expressed at low levels, thus reducing the splicing variability in prostate cancer.

Dr Rajan said: “This unique finding has never been shown before for a controller of alternative splicing and may mean that FOXA1 directs prostate cancer cells to act in a particular way that may be detrimental to patients.”
Co-senior author Professor Matteo Cereda, Associate Professor at the University of Milan and Group Leader at the Italian Institute for Genomic Medicine, added: “For the first time we show that an early player of transcription regulation is also responsible for the fine tuning of alternative splicing.”

Potential new targets for treatment

To determine whether FOXA1-controlled alternative splicing had an impact on patient survival, the team analysed clinical data from over 300 patients with primary prostate cancer, available via The Cancer Genome Atlas.

Although high levels of FOXA1 reduced splicing variability, the team found that FOXA1 enhanced the inclusion of genetic segments into splice variants that are strong markers of prostate cancer recurrence. Using prostate cancer cell lines, the team revealed that the inclusion of one particular genetic segment in the splice variant of a gene called the FLNA gene, which is controlled by FOXA1, conferred a growth advantage to prostate cancer cells, which may drive early disease relapse.

Dr Rajan said: “This study illustrates how we can exploit the power of genomics to make important scientific discoveries about how genetic variability in prostate cancer is controlled. We hope our findings will have clinical impact by identifying more precise markers of disease recurrence and new potential drug targets.”

The researchers would now like to explore if the splice variations associated to cancer recurrence are beneficial in predicting disease relapse in reality, as well as conduct tests to see if targeting these genes might represent new strategies to treat prostate cancer.

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