WEHI researchers have solved a mystery about the most important driver of cancer development – a mutant protein found in half of all cancers – and how it contributes to tumour growth.
The p53 protein is a tumour suppressor that plays a crucial role in preventing the formation of cancerous cells. But when it mutates and becomes defective in cells, the protein can significantly boost a person’s risk of cancer development.
In a first, researchers have revealed what behaviours of the mutated protein are critical for fuelling tumour growth – a discovery that could offer new directions for the development of treatment options.
When it works properly, the p53 protein serves as a powerful defence mechanism against cancer development by ensuring that cells with compromised DNA either get repaired or removed from our body.
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Mutations to this protein can be triggered by a variety of environmental factors – such as exposure to UV radiation – if the body’s cell division process goes awry, or if they are genetically inherited.
These abnormalities can lead to a dysfunctional protein that has lost the crucial ability to regulate cellular responses that prevent tumour development and growth. This is known as loss-of-function.
Additionally, some researchers believe these mutations can also lead to a supercharged protein that helps cancerous cells survive and proliferate, known as gain-of-function.
In a new study, published in Cancer Discovery, researchers from WEHI and Trento University (Italy) have answered an age-old question by proving which function helps mutant p53 fuel tumour growth.
Associate Professor Gemma Kelly, a co-corresponding author of the paper, said understanding how exactly these mutations contribute to cancer is critical to understanding how to treat patients bearing cancers with the dysfunctional proteins.
“Our study has provided the first evidence to show that it is actually the loss-of-function that impacts cancer growth. We found no evidence of gain-of-function contributing to cancer growth,” Assoc Prof Kelly, a Laboratory Head in WEHI’s Blood Cells and Blood Cancer Division, said.
“This is significant because until now, there was not much evidence available to properly show whether it is the protein’s loss or gain-of-function that spurs cancer growth.
“If you look at all cancers of humanity, about 50% of them have a mutation in p53. Specific cancers like those of the pancreas, lung and breast, commonly have defects in these proteins.”
“Our findings have transformed our understanding of these mutations, which help rethink how they can be targeted in the development of new cancer treatments.” Associate Professor Gemma Kelly
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Co-corresponding author, Professor Andreas Strasser, said the findings could prevent hundreds of millions of dollars being wasted on developing ineffective drugs.
“There is research underway that is working towards finding the first therapeutics to target gain-of-function traits,” Prof Strasser, Head of WEHI’s Blood Cells and Blood Cancer Division, said.
“Our findings indicate there is no further merit in this therapeutic avenue and the focus needs to shift to restoring the mutant protein’s lost function and normal tumour suppressor ability.”
Paper: Wang Z, Burigotto M, Ghetti S, et al. Loss-of-function but not gain-of-function properties of mutant TP53 are critical for the proliferation, survival and metastasis of a broad range of cancer cells. Cancer Discovery. 2023. doi: 10.1158/2159-8290.CD-23-0402
