A molecular glue degrader of the WIZ transcription factor for fetal hemoglobin induction
2024; American Association for the Advancement of Science; Volume: 385; Issue: 6704 Linguagem: Inglês
10.1126/science.adk6129
ISSN1095-9203
AutoresPamela Y. Ting, Sneha Borikar, John Ryan Kerrigan, Noel M. Thomsen, Eamon Aghania, Amelia E. Hinman, Alejandro Reyes, Nicolas Pizzato, Barna D. Fodor, Fabian Wu, Muluken S. Belew, Xiaohong Mao, Jian Wang, Shripad Chitnis, Wei Niu, Amanda Hachey, Jennifer Cobb, Nikolas A. Savage, Ashley Burke, Joshiawa Paulk, Dustin Dovala, James A. Lin, Matthew C. Clifton, Elizabeth Ornelas, Xiaolei Ma, Nathaniel F. Ware, Carina C. Sanchez, John A. Taraszka, Rémi Terranova, Judith Knehr, Marc Altorfer, S. Whitney Barnes, Rohan E. J. Beckwith, Jonathan M. Solomon, Natalie A. Dales, Andrew W. Patterson, J. Wagner, Tewis Bouwmeester, Glenn Dranoff, Susan C. Stevenson, James E. Bradner,
Tópico(s)RNA modifications and cancer
ResumoSickle cell disease (SCD) is a prevalent, life-threatening condition attributable to a heritable mutation in β-hemoglobin. Therapeutic induction of fetal hemoglobin (HbF) can ameliorate disease complications and has been intently pursued. However, safe and effective small-molecule inducers of HbF remain elusive. We report the discovery of dWIZ-1 and dWIZ-2, molecular glue degraders of the WIZ transcription factor that robustly induce HbF in erythroblasts. Phenotypic screening of a cereblon (CRBN)-biased chemical library revealed WIZ as a previously unknown repressor of HbF. WIZ degradation is mediated by recruitment of WIZ(ZF7) to CRBN by dWIZ-1, as resolved by crystallography of the ternary complex. Pharmacological degradation of WIZ was well tolerated and induced HbF in humanized mice and cynomolgus monkeys. These findings establish WIZ degradation as a globally accessible therapeutic strategy for SCD.
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