Missing Hormone Gene Linked to Incurable Prostate Cancer
Lead Author Nima Sharifi, M.D. Credit: Cleveland Clinic
A study led by researchers at the Cleveland Clinic Medical Center has shown a mechanistic link between the loss of a gene subtype that limits male hormones and incurable prostate cancer.
The research, led by Nima Sharifi, M.D. of the Cleveland Clinic’s Lerner Research Institute, built upon their earlier seminal work in which they discovered that a gene called HSD3B1, when altered, enables prostate tumors to evade treatment and proliferate. They went on to show that the presence of this gene variant does in fact change treatment outcomes and overall survival in men.
In the current study published in Journal Cell Reports, Dr. Sharifi and his team studied a related gene, called HSD17B4. Previous research showed that HSD17B4 encodes enzymes that inactivate androgens (male hormones). Since androgens are essential for prostate cancer growth, inactivating them should prevent cancer advancement. But these enzymes have also been observed to be more abundant in advanced prostate cancer. Therefore, until now it remained unclear whether the enzymes promote or suppress prostate cancer.
Therapy for advanced prostate cancer—called androgen deprivation therapy (ADT), or chemical castration—blocks cells’ supply of androgens, which they use as fuel to grow and spread. While ADT is successful early on, it eventually fails, allowing the cancer to progress to a lethal phase called castration-resistant prostate cancer (CRPC).
“We are hopeful that these findings will lead to more precise and effective treatments for prostate cancer,” said Dr. Sharifi. “If men lack a specific isoform of this gene, we may be able to personalize their therapy.”
To determine HSD17B4’s role in the transition to CRPC, Dr. Sharifi’s team analyzed its expression in tissue from patients with healthy prostates, localized prostate cancer and CRPC. They found that HSD17B4 expression levels were relatively the same in benign and local prostate cancer tissue, but significantly reduced in CRPC tissue, suggesting that HSD17B4 does play a role in preventing progression to CRPC.
Through a series of analyses, the researchers found that only one specific isoform of HSD17B4—isoform 2—enzymatically inactivated androgens and prevented tumor growth. It is expressed during the early phases of prostate cancer, but is lost, or suppressed, in CRPC (advanced prostate cancer). Isoforms vary in amino acid sequence and physiological function, but not DNA code.
The team also validated their findings in a preclinical model. Their findings suggest that lack of isoform 2 leads to advanced CRPC. Additional research will be important to determine how HSD17B4 becomes silenced in CRPC and whether it may be used as a biomarker for patients at risk of dying from prostate cancer.
Schizophrenics' Blood Contains RNA From More MicrobesNews
The blood of schizophrenia patients features genetic material from more types of microorganisms than that of people without the debilitating mental illness, research at Oregon State University has found. What’s not known is whether that’s a cause or effect of the severe, chronic condition that strikes about one person in 100.READ MORE
Antitumor Immune Function in Liver Controlled by Gut MicrobiomeNews
Scientists have found a connection between bacteria in the gut and antitumor immune responses in the liver. The study showed that bacteria found in the gut of mice affect the liver’s antitumor immune function. The findings have implications for understanding the mechanisms that lead to liver cancer and for therapeutic approaches to treat them.READ MORE
Comments | 1 ADD COMMENT
carmelo v | Jan 23, 2018
Tests are vital and needed in early detection. My dad was diagnosed with BPH which is normal on his middle 50s, he wasnt able to sleep well because of his urges to pee, also he experienced pain when he had to pee he found this one called Alpha rise and took matters into hisown hands doing prostate supplement research. It seems to have everything he needed