Small-molecule probe reveals a kinase cascade that links stress signaling to TCF/LEF and Wnt responsiveness

• Published in: Cell chemical biology Vol. 28; no. 5; pp. 625 - 635.e5
• Main Authors: Cheng, Jiongjia, Tsuda, Masanao, Okolotowicz, Karl, Dwyer, Mary, Bushway, Paul J., Colas, Alexandre R., Lancman, Joseph J., Schade, Dennis, Perea-Gil, Isaac, Bruyneel, Arne A.N., Lee, Jaechol, Vadgama, Nirmal, Quach, Justine, McKeithan, Wesley L., Biechele, Travis L., Wu, Joseph C., Moon, Randall T., Si Dong, P. Duc, Karakikes, Ioannis, Cashman, John R., Mercola, Mark
• Format: Journal Article
• Language: English
• Published: United States Elsevier Ltd 20.05.2021
• Subjects: Animals; ataxia telangiectasia mutated/ATM; Aurora kinases; beta Catenin - antagonists & inhibitors; beta Catenin - genetics; beta Catenin - metabolism; Cells, Cultured; homeodomain-interacting protein kinase/HIPK2; Humans; LEF; Male; Molecular Probes - chemistry; Molecular Probes - pharmacology; p53; Protein Serine-Threonine Kinases - metabolism; Small Molecule Libraries - chemistry; Small Molecule Libraries - pharmacology; TCF; TCF Transcription Factors - antagonists & inhibitors; TCF Transcription Factors - genetics; TCF Transcription Factors - metabolism; Wnt; Wnt Signaling Pathway - drug effects; Xenopus; Zebrafish; β-catenin; β-catenin; Aurora kinases; TCF; homeodomain-interacting protein kinase/HIPK2; Wnt; LEF; ataxia telangiectasia mutated/ATM; p53
• ISSN: 2451-9456; 2451-9448; 2451-9456
• DOI: 10.1016/j.chembiol.2021.01.001

Wnt signaling plays a central role in tissue maintenance and cancer. Wnt activates downstream genes through β-catenin, which interacts with TCF/LEF transcription factors. A major question is how this signaling is coordinated relative to tissue organization and renewal. We used a recently described class of small molecules that binds tubulin to reveal a molecular cascade linking stress signaling through ATM, HIPK2, and p53 to the regulation of TCF/LEF transcriptional activity. These data suggest a mechanism by which mitotic and genotoxic stress can indirectly modulate Wnt responsiveness to exert coherent control over cell shape and renewal. These findings have implications for understanding tissue morphogenesis and small-molecule anticancer therapeutics. [Display omitted] •PAWI-1,2 are small molecules with dual p53 agonist and Wnt inhibitor activities•PAWIs bind tubulin and activate stress signaling•Stress signaling through ATM, AURK, and HIPK inhibits TCF/LEF transcriptional activity•PAWIs inhibit the ability of a cell to respond to Wnt Cheng et al. used high-throughput screening to identify a small molecule with dual p53 agonist and Wnt inhibitory activity. Named PAWI, the compounds were used to trace a kinase cascade linking stress signaling to the regulation of TCF/LEF function and the control of Wnt-dependent gene expression.