Genome Study Yields Insights Into Bladder Cancer – NIH …

Posted: February 7, 2014 at 5:43 pm

February 3, 2014

Researchers identified genes and pathways that are disrupted in a major form of bladder cancer. The study also revealed subtypes that resemble other cancers at a molecular level, implying similar routes of development. The findings suggest potential new therapeutic targets.

Bladder canceralso known as urothelial carcinomais expected to cause more than 15,000 deaths in the United States in 2014. About 72,000 new cases will be diagnosed this year as well.

Bladder cancer that invades the muscle of the bladder is the deadliest form of the disease. Standard treatments for muscle-invasive bladder cancer include surgery and radiation combined with chemotherapy. There are no recognized follow-up treatments if the initial therapy doesnt work.

To gain a better understanding of this cancer, investigators in The Cancer Genome Atlas (TCGA) Research Network undertook a comprehensive genomic analysis of 131 muscle-invasive bladder carcinomas from patients who hadnt yet been treated. The researchers analyzed DNA, RNA, and protein data. TCGA is supported by NIHs National Cancer Institute (NCI) and National Human Genome Research Institute (NHGRI). The study appeared online on January 29, 2014, in Nature.

The scientists found recurrent mutations in 32 genes, including 9 that werent previously reported to be significantly mutated in any cancer. They identified mutations in the TP53 gene in nearly half the tumor samples. TP53 codes for the p53 tumor suppressor protein, which helps regulate cell division. The RTK/RAS pathway, which is involved in regulating cell growth and developmentand is affected in many cancerswas altered in 44% of the tumors analyzed.

Genes that regulate chromatinthe DNA/protein structure that determines how genes are expressedwere more frequently mutated in bladder cancer than in any other common cancer studied to date. These findings suggest the possibility of developing therapies that target chromatin remodeling.

The researchers identified potential drug targets in 69% of the tumors evaluated. Of note were frequent mutations in the ERBB2, or HER2, gene. HER2 has been implicated in a significant portion of breast cancers. New therapeutic agents under development against breast cancer thus might be effective in treating certain bladder cancers.

The scientists uncovered a potential viral connection to bladder cancer as well. DNA from virusesnotably, from HPV16, a form of the virus responsible for cervical cancerwas found in a small number of bladder tumors. This suggests that viral infection may contribute to the development of bladder cancer.

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