Anticancer drug candidate inhibits lethal aggregation of mutant tumor suppressor protein

Anticancer drug candidate inhibits lethal aggregation of mutant tumor suppressor protein
PRIMA-1/MQ effects on amyloid-state p53. 1) PRIMA-1 mobilizes the aggregated p53 pool and stabilizes mutant p53, resulting in the recovery of wild-type p53 functions and in the reduction of the cellular amyloid content. 2) PRIMA-1/MQ blocks the seeding of wild-type p53C aggregation by mutant p53 present in cell lysates, which might be part of the general effect of PRIMA-1/MQ on p53 seen in mutant p53 cancer cells. Credit: Luciana P. Rangel and Giulia D. S. Ferretti

Cancer is a multidisciplinary disease, with different mutations leading to different prognoses and treatment necessities. Among the most important mutation targets in cancers, affecting more than 50 percent of all cancer cases, is TP53. This gene gives rise to a protein that is a key regulator in the cell, called p53. When mutated, this protein forms amyloid structures that accumulate in the cell, causing cancers that tend to have a worse prognosis. A group of Brazilian researchers has shown that a synthetic compound, PRIMA-1, reverses mutant p53 aggregate accumulation. The novel study is the first to demonstrate the action of PRIMA-1 on the inhibition of aggregates of the mutant p53 protein. The results are published in the Journal of Biological Chemistry.

Mutations in the TP53 gene will kill hundreds of million people alive today if new therapies are not developed. Mutant p53 not only undergoes misfolding but also aggregation, similar to that observed with amyloids, playing a crucial role in the development of cancer through loss of function, negative dominance and gain of function. In earlier studies, researchers led by Jerson Silva at the Federal University of Rio de Janeiro (UFRJ) have pointed out that mutant p53 aggregation is an excellent target for development of therapeutic drugs against cancer.

Now, the same group shows that PRIMA-1 (p53 reactivation with induction of massive apoptosis-1) and its primary active metabolite, 2-methylene-3-quinuclidinone (MQ), can restore aggregated mutant p53 to a native form. PRIMA-1 and MQ had been previously shown to convert unfolded p53 mutants to a native conformation that induces apoptosis and activates several p53 target genes. This study provides the first demonstration that PRIMA-1 can rescue amyloid-state p53 mutants, a strategy that could be further explored as a cancer treatment. Its derivative PRIMA-1MET is now in Phase II and the Brazilian results may contribute to the development of a new anticancer drug. The research was conducted in vitro and in tumor cell lines of breast cancer and ovarian carcinoma.

"The findings are crucial in establishing the mutant p53 aggregation as a highly promising target for therapy and we are working hard on this subject," states Luciana P. Rangel, first author of the study, from the Faculty of Pharmacy of UFRJ and a member of the National Institute of Science and Technology of Structural Biology and Bioimaging (INBEB).

More information: Luciana P. Rangel et al, p53 reactivation with induction of massive apoptosis-1 (PRIMA-1) inhibits amyloid aggregation of mutant p53 in cancer cells, Journal of Biological Chemistry (2019). DOI: 10.1074/jbc.RA118.004671

Journal information: Journal of Biological Chemistry
Provided by Instituto Nacional de Ciência e Tecnologia de Biologia Estrutural e Bioimagem (INBEB)
Citation: Anticancer drug candidate inhibits lethal aggregation of mutant tumor suppressor protein (2019, January 15) retrieved 19 April 2024 from
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