An international research team used a novel statistical model to find 27 new genes thought to prevent cancer from occurring. The findings could help create new cancer therapies that target these genes, and open up other avenues of cancer research, say the scientists.
“Using this powerful toolkit, we've uncovered rare tumor suppressor genes that when lost in mutated cells, cause cancer,” says Jonas Demeulemeester, Ph.D., joint first author of the paper and researcher at the Francis Crick Institute. “This could pave the way for the development of personalized cancer treatments.”
The study (“Pan-Cancer Analysis of Homozygous Deletions in Primary Tumors Uncovers Rare Tumor Suppressors”), published in Nature Communications, was led by scientists at the Francis Crick Institute and the University of Leuven, in collaboration with the University of Chicago and the University of Oslo.
“Homozygous deletions are rare in cancers and often target tumour suppressor genes. Here, we build a compendium of 2218 primary tumours across 12 human cancer types and systematically screen for homozygous deletions, aiming to identify rare tumour suppressors. Our analysis defines 96 genomic regions recurrently targeted by homozygous deletions. These recurrent homozygous deletions occur either over tumour suppressors or over fragile sites, regions of increased genomic instability. We construct a statistical model that separates fragile sites from regions showing signatures of positive selection for homozygous deletions and identify candidate tumour suppressors within those regions,” write the investigators.
“We find 16 established tumour suppressors and propose 27 candidate tumour suppressors. Several of these genes (including MGMT, RAD17, and USP44) show prior evidence of a tumour suppressive function. Other candidate tumour suppressors, such as MAFTRR, KIAA1551, and IGF2BP2, are novel. Our study demonstrates how rare tumour suppressors can be identified through copy number meta-analysis.”
Studying double tumor suppressor gene copy deletions can provide important clues on cancer development. However, cancer samples normally contain both healthy cells and cancerous cells in unknown proportions, making it difficult to work out if just a single copy or both copies of the gene have been lost in the cancer cells. In addition, it can be difficult to distinguish between harmful deletions of tumor suppressor genes and nonharmful deletions of other genes at fragile sites along the genome.
The team developed computational tools to overcome these issues and used them to analyze 2218 tumors from 12 cancer types, including breast, lung, and bowel cancers. By determining the relative proportions of cancerous and healthy cells in each sample, they could work out the number of copies of each gene in the cancer cells. This analysis revealed 96 regions of the human genome that are frequently lost during tumor development.
The analysis also revealed that harmful tumor suppressor gene deletions have a different DNA footprint from nonharmful deletions, which tend to be much smaller. This enabled the researchers to categorize the 96 deletions, revealing 16 previously known tumor suppressor genes, and 27 new ones, as noted in their journal paper. Some of these had previously been suspected to contribute to cancer development, while others were completely new.
“Our study demonstrates that rare tumor suppressor genes can be identified through large-scale analysis of the number of copies of genes in cancer samples,” says Peter Van Loo, Ph.D., senior author of the paper and group leader at the Francis Crick Institute. “Cancer genomics is a growing area of research, and the computational tools we use are a powerful way to find new genes involved in cancer.”
The new candidate tumor suppressor genes identified in this study can be investigated by scientists in the laboratory to understand their mechanism of action and try to find drug targets, he adds.
