A triple-action PROTAC for wild-type p53 cancer therapy

Despite the central role of p53 suppression in cancer pathogenesis, the promise of therapeutic p53 reactivation remains unrealized, with targeted and combination chemotherapies limited by efficacy, toxicity, and delivery. To overcome these challenges, we introduce a triple-action proteolysis targeting chimera (TAPTAC) that simultaneously targets three oncogenic mechanisms to reactivate apoptosis. TAPTAC1 diverts HDM2 from degrading p53 to eliminating oncogenic targets such as BET proteins, while also blocking HDMX-mediated sequestration, thereby maximizing p53 reactivation in concert with cancer protein degradation. TAPTAC1 outperforms combination treatments and PROTACs that target HDM2 and BET proteins, but not HDMX, and is broadly effective in wild-type (WT) p53 cancers, including mouse models of osteosarcoma and leukemia. Importantly, TAPTAC1 leverages cancer dependency on HDM2 to enhance selectivity and mitigate toxicity. With WT p53 retained in 90% of pediatric and 50% of adult cancers, TAPTACs provide a therapeutic platform for addressing key limitations of prior anti-cancer strategies.

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Publication Details

Journal
Cell Reports Medicine
Published
2025-11-26
DOI
https://doi.org/10.1016/j.xcrm.2025.102467
Primary Topic
Protein Degradation and Inhibitors
Type
article
Field-Weighted Citation Impact
0.00

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article

A triple-action PROTAC for wild-type p53 cancer therapy

Ruitong Li, Marina Godes, Loren D. Walensky, Mauricio Menacho-Márquez et al.
Cell Reports Medicine
Protein Degradation and Inhibitors
article

A triple-action PROTAC for wild-type p53 cancer therapy

Ruitong Li, Marina Godes, Loren D. Walensky, Mauricio Menacho-Márquez, João A. Paulo, Michael D. Cameron, Thomas M. DeAngelo, Utsarga Adhikary, Gregory H. Bird, J. Michael Schmidt, Bethany Tesar, Steven P. Gygi, Prafulla C. Gokhale, Christina M. Camara, Shannan J. Ho Sui, Julia F Vidlak
article en

Abstract

Despite the central role of p53 suppression in cancer pathogenesis, the promise of therapeutic p53 reactivation remains unrealized, with targeted and combination chemotherapies limited by efficacy, toxicity, and delivery. To overcome these challenges, we introduce a triple-action proteolysis targeting chimera (TAPTAC) that simultaneously targets three oncogenic mechanisms to reactivate apoptosis. TAPTAC1 diverts HDM2 from degrading p53 to eliminating oncogenic targets such as BET proteins, while also blocking HDMX-mediated sequestration, thereby maximizing p53 reactivation in concert with cancer protein degradation. TAPTAC1 outperforms combination treatments and PROTACs that target HDM2 and BET proteins, but not HDMX, and is broadly effective in wild-type (WT) p53 cancers, including mouse models of osteosarcoma and leukemia. Importantly, TAPTAC1 leverages cancer dependency on HDM2 to enhance selectivity and mitigate toxicity. With WT p53 retained in 90% of pediatric and 50% of adult cancers, TAPTACs provide a therapeutic platform for addressing key limitations of prior anti-cancer strategies.

Cell Reports MedicineVol. 6(12)
Broad Institute (US), Scripps Research Institute (US), Harvard University (US), Dana-Farber Cancer Institute (US), Dana-Farber/Harvard Cancer Center (US)
Alex's Lemonade Stand Foundation for Childhood Cancer, Harvard Catalyst, Dana-Farber/Harvard Cancer Center, Broad Institute, William Lawrence and Blanche Hughes Foundation, National Institutes of Health
Openalex Percentile: Top 67%
Protein Degradation and Inhibitors
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