PT - JOURNAL ARTICLE AU - Wei Tang AU - Yu Wu AU - Xin Qi AU - Rilei Yu AU - Zhimin Lu AU - Ao Chen AU - Xinglong Fan AU - Jing Li TI - PGK1-coupled HSP90 stabilizes GSK3β expression to regulate the stemness of breast cancer stem cells AID - 10.20892/j.issn.2095-3941.2020.0362 DP - 2022 Apr 15 TA - Cancer Biology & Medicine PG - 486--503 VI - 19 IP - 4 4099 - http://www.cancerbiomed.org/content/19/4/486.short 4100 - http://www.cancerbiomed.org/content/19/4/486.full SO - Cancer Biology & Medicine2022 Apr 15; 19 AB - Objective: Glycogen synthase kinase-3β (GSK3β) has been recognized as a suppressor of Wnt/β-catenin signaling, which is critical for the stemness maintenance of breast cancer stem cells. However, the regulatory mechanisms of GSK3β protein expression remain elusive.Methods: Co-immunoprecipitation and mass spectral assays were performed to identify molecules binding to GSK3β, and to characterize the interactions of GSK3β, heat shock protein 90 (Hsp90), and co-chaperones. The role of PGK1 in Hsp90 chaperoning GSK3β was evaluated by constructing 293T cells stably expressing different domains/mutants of Hsp90α, and by performing a series of binding assays with bacterially purified proteins and clinical specimens. The influences of Hsp90 inhibitors on breast cancer stem cell stemness were investigated by Western blot and mammosphere formation assays.Results: We showed that GSK3β was a client protein of Hsp90. Hsp90, which did not directly bind to GSK3β, interacted with phosphoglycerate kinase 1 via its C-terminal domain, thereby facilitating the binding of GSK3β to Hsp90. GSK3β-bound PGK1 interacted with Hsp90 in the “closed” conformation and stabilized GSK3β expression in an Hsp90 activity-dependent manner. The Hsp90 inhibitor, 17-AAG, rather than HDN-1, disrupted the interaction between Hsp90 and PGK1, and reduced GSK3β expression, resulting in significantly reduced inhibition of β-catenin expression, to maintain the stemness of breast cancer stem cells.Conclusions: Our findings identified a novel regulatory mechanism of GSK3β expression involving metabolic enzyme PGK1-coupled Hsp90, and highlighted the potential for more effective cancer treatment by selecting Hsp90 inhibitors that do not affect PGK1-regulated GSK3β expression.