Researchers identified a set of cis-regulatory elements – namely enhancers and the promoter – in the non-coding region of the genome, which affect the expression of FOXA1 gene, one of the major drivers or oncogenes involved in prostate cancer development.
FOXA1 has long been recognized as playing an important role in malignancy, but it is one of the most challenging targets for drug development in cancer.
Often termed “undruggable,” it is extremely difficult to inhibit due to its lack of easily accessible “pockets” for small molecule therapies to slip into to break the deadly uncontrolled cell growth leading to cancer.
Scientists the world over are looking at different ways to target FOXA1, since it is implicated in many cancers including breast, prostate, lung, thyroid and esophageal squamous cell carcinomas.
“To track a tumour, we also have to look at the non-coding space in its DNA because that’s where gene expression – the switching on or off of a gene – happens,” explains Dr. Mathieu Lupien, Senior Scientist at Princess Margaret Cancer Centre and the senior author of this latest research.
“We can’t dismiss what’s going on in the non-coding space because that is what fuels differences in expression in genes. To fully understand a tumour, we have to explore the whole genome – the genes and the non-coding space.”
Scientists have begun mining the dark or non-coding portion of the genome – about 98 per cent of the genome – as a potential source of new targets for drug development.
Dr. Lupien, who is also an assistant professor with the University of Toronto’s Department of Medical Biophysics, is one of the first researchers to realize that hidden amongst the non-coding DNA are crucial elements that not only control the activity of thousands of genes, but also play a major role in many diseases. Exploring this area could provide important sequencing clues for potential cures.
Dr. Lupien’s current research, entitled “Noncoding mutations target cis-regulatory elements of the FOXA1 plexus in prostate cancer” is published in Nature Communications, Jan. 23.
The research team examined 200 human prostate tumours and identified six mutated cis-regulatory elements which control FOXA1 expression. They further demonstrated that removing these elements reduced FOXA1 expression and impaired growth of prostate cancer cells.
“Because of the difficulties in targeting FOXA1 with drugs, we had to find alternative targets to block its function,” says Dr. Lupien. “We found these targets by identifying regulatory elements in the non-coding DNA required for FOXA1 expression.”
This allows us to expand our tool kit of potential therapies against prostate cancer, adds Dr. Lupien, because this regulatory web represents a more precise target against cancer.
Prostate cancer is the second most commonly diagnosed malignancy among men worldwide, with an estimated 1.3 million new cases worldwide in 2018.
In Canada, it is estimated that in 2019:
- 22,900 men will be diagnosed with prostate cancer. This represents 20 per cent of all new cancer cases in men in 2019.
- 4,100 men will die from prostate cancer. This represents nine per cent of all cancer deaths in men in 2019.
Treatments typically fail in 30 per cent of patients within 10 years, resulting in cancer spreading to other sites. Despite the efficacy of anti-androgen therapies for metastatic cancer, recurrence ultimately develops into a lethal cancer. This spurs our need to improve our biological understanding of how prostate cancer develops, and to find novel strategies to treat patients.
This research is supported by the Canadian Institutes of Health Research, Prostate Cancer Canada (Movember), Ontario Institute for Cancer Research, Princess Margaret Cancer Foundation, Canadian Cancer Society, Terry Fox Research Institute and the Dutch Cancer Society KWF/Alpe d’HuZes.
Original post https://alertarticles.info