Genetic variations linked to increased PCa risk identified

Article

The findings could help clinicians differentiate between slow-growing and aggressive tumors

Findings from a large international study have identified 22 genetic variations that are associated with an increased risk of developing prostate cancer.

READ: FDA approves label update for advanced PCa treatment

The study, which was published in Cancer Discovery (2015; 5:358-79), was conducted by the PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) consortium, whose goal is to identify genetic risk factors associated with prostate cancer.

Men who have a family history of prostate cancer have a two-fold greater risk of developing the disease. Currently, approximately 100 genetic variants have been found to influence the risk of prostate cancer. However, these variants only account for 33% of increased familial risk, suggesting that additional genetic factors must also exist, according to a press release from Moffitt Cancer Center in Tampa, FL, which participated in the study.

The researchers compared the genetic information from 22,301 prostate cancer cases and 22,320 normal control cases from 23 different clinical studies. The research team focused their analysis on microRNAs.

The authors discovered 22 microRNA binding site variations that influence the risk of developing prostate cancer. Among these 22 variations, 10 of them were not investigated thoroughly as being potential risk factors. Seven of the variants could differentiate between aggressive and nonaggressive disease.

NEXT: One variant plays role in mediating expression of PSA

More from Urology Times

Androgen receptor inhibitor shows significant PFS increase

Sexual effects data lacking on 5-ARI for hair loss

Study: Low-dose-rate BT outperforms EBRT boost

 

The authors further confirmed the importance of two of these genetic variants by investigating how they influence protein expression in normal and cancerous prostate tissue. They discovered that one of the variants plays an important role in mediating expression of PSA, and the second variant controls expression of a gene involved in metabolism.

ALSO SEE: Significant OS improvement seen with mCRPC Tx vs. placebo

“The hope is that this research may eventually lead to a simple genotyping based blood test that could be used in conjunction with the PSA and DRE tests to aid the medical team and patient in accurately predicting disease risk,” said co-author Jong Park, PhD, of Moffitt Cancer Center.

The results from this study may also allow physicians to differentiate between slow-growing and aggressive prostate tumors and aid in therapeutic decisions.

You might also like:

European data on PCa assay comparable to U.S. findings

Study uncovers 400% cost difference in BPH treatments

Workplace exertion among factors linked to male infertility

To get weekly news from the leading news source for urologists, subscribe to the Urology Times eNews.
 

Related Videos
Prostate cancer, 3D illustration showing presence of tumor inside prostate gland which compresses urethra | Image Credit: © Dr_Microbe - stock.adobe.com
Doctor consulting with patient | Image Credit: © Khunatorn - stock.adobe.com
Scott Morgan, MD, MSc, FRCPC, answers a question during a Zoom video interview
Man talking with a doctor | Image Credit: © Chinnapong - stock.adobe.com
Todd M. Morgan, MD, answers a question during a Zoom video interview
3D illustration of prostate cancer cells | Image Credit: © Dr_Microbe - stock.adobe.com
Brian T. Helfand, MD, and Matthew Smith, MD, PhD, experts on prostate cancer
Brian T. Helfand, MD, and Matthew Smith, MD, PhD, experts on prostate cancer
Matthew Loria answers a question during a Zoom video interview
Blur image of hospital corridor | Image Credit: © whyframeshot - stock.adobe.com
Related Content
© 2024 MJH Life Sciences

All rights reserved.