One of the most extensively studied genes in cancer, TP53 is well known for its role as a tumor suppressor. It senses cellular stress or damage, and in response stops cell division or initiates cell death, thereby preventing a damaged cell from reproducing. Mutation of this gene eliminates a key cellular fail-safe mechanism and is a step leading to cancer.
Researchers have conducted the most comprehensive study of TP53 mutations to better understand the processes leading to the inactivation of this important gene. Their findings, published in the journal Cell Reports, shed light on how the gene becomes mutated and how those mutations can help predict clinical outlook.
The team studied 10,225 patient samples from 32 different cancers, from The Cancer Genome Atlas, and compared them to another 80,000 mutations in a database. After analyzing this large data sample, they have a more thorough understanding of how the TP53 gene mutation impacts cancer.
The team found that across all cancer types studied, TP53 mutations were more frequent in patients with poorer survival rates. But they also identified a way to more accurately predict prognosis. The senior author said they identified four upregulated genes in mutant TP53 tumors, whose expression correlated to patient outcome.
"If you have a high expression of those four genes, you have a patient who's more likely to have a bad prognosis," the senior author said. "Conversely, if that patient has a very low expression of those genes, he's probably going to survive longer and have a good prognosis. It will give you a better picture of how he'll fare than just knowing whether he's mutant for TP53 or not."
At the chromosomal level, the team found a noticeable pattern in TP53 gene loss.
"In some cancer genes, you'll see one copy of the two genes lost or mutated," the senior author said. "Over 91 percent of all cancers lose both TP53 genes, not just one."
This second gene loss occurred due to mutation, chromosomal deletion or gene duplication. According to the senior author, cases of gene duplication occurred at a much higher rate than previously thought.
The research also showed that TP53 mutation correlated strongly with genomic instability, indicative of the role of the normal protein in monitoring chromosome integrity. In most TP53 mutant tumors, other tumor suppressor genes were deleted, while oncogenes that allow cancer to develop were amplified.
While many studies have been conducted on TP53, this is the first to examine such a large number of tumors and cancer types using five different data collection methods. "Most studies on TP53 focus on one cancer type," the senior author said. "Looking at 32 different cancer types, you see that certain patterns hold up regardless of cancer type."
How the TP53 gene mutation impacts cancer
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