Study Identifies 'Lethal' Subtype Of Prostate Cancer

Study identifies 'lethal' subtype of prostate cancer
Prostate cancer cells (Image source)
A new study published in the journal Cancer Research defines a new, distinct subtype of "lethal" prostate cancer marked by the loss of two genes, MAP3K7 and CHD1. Overall about 10 percent of men with prostate cancer will die from the disease. The study shows that of prostate cancer patients with combination MAP3K7 and CHD1 deletions, about 50 percent will have recurrent prostate cancer, which ultimately leads to death. About 10 percent of all prostate cancers harbor combined MAP3K7-CHD1 deletions.
 
The researchers started with the long-known observation that some prostate cancers tend to be slow-growing and less dangerous, whereas others tend to be fast-growing and dangerous. The question was whether there is a genetic difference between aggressive and less aggressive prostate cancers. Analysis of tumor samples from publicly available databases showed that MAP3K7-CHD1 loss was a major genetic marker of cancers that eventually went on to be of the aggressive type, possibly accounting for 25 percent of prostate cancer-related death. That is about 7,500 men per year. The research then used a sophisticated stem-cell model to grow artificial prostate tumors with these gene deletions that were implanted in mice.
 
The researchers grew mouse prostate stem cells in culture in which they knocked down these two genes. Then they combined these engineered stem cells with prostate cells to make artificial prostates and graft them into the mouse models. This allowed them to prospectively watch the growth of prostates to see the effects of these specific genetic changes.
 
In fact, these artificial prostate glands grown in mice developed aggressive cancer similar to what was seen in the database of human cancers. Specifically, loss of the genes MAP3K7 and CHD1 "greatly disrupted" the ability of prostate stem cells to create healthy prostate tissue, while instead they created cancerous cells with characteristics of "neuroendocrine and neural" cells. In other words, this genetic change made stem cells that should create healthy prostate tissue instead create hybrid-type cells that break many of the speed controls governing replication and growth. It is these hybrid cells that act aggressively cancerous.
 
The goal now is to discover ways to target these lethal prostate cancer cells. This first includes a "synthetic lethal" screen that tests thousands of drug candidates against cells with MAP3K7-CDH1 deletions to identify drugs that selectively kill cells with these deletions. The researchers also plan additional testing to further refine the prognostic ability of testing for these deletions.
 
Based on material originally posted by University of Colorado Denver.