| Journal of Hematology & Oncology | |
| GSK3-beta as a candidate therapeutic target in soft tissue sarcomas | |
| L. Cavalcante1  F. Giles1  R. Perret2  V. Velasco2  E. Richard3  V. Chaire4  A. Italiano4  S. Verbeke4  | |
| [1] Actuate Therapeutics;Department of Pathology, Institut Bergonié;INSERM, U1218;Sarcoma Unit, Institut Bergonié; | |
| 关键词: Glycogen synthase kinase 3β; Soft tissue sarcomas; 9-ING-41; | |
| DOI : 10.1186/s13045-021-01215-x | |
| 来源: DOAJ | |
【 摘 要 】
Abstract Soft tissue sarcoma (STS) is a predominantly fatal rare malignancy with inadequate treatment options. Glycogen synthase kinase 3β (GSK-3β) is an emerging target in human malignancies. Its therapeutic relevance in STS is unknown. We analyzed the prognostic impact of GSK-3β gene and protein expression in two independent cohorts of patients with STS. We then treated STS cell lines and mice xenografts with a novel GSK-3 inhibitor 9-ING-41 alone or in combination with chemotherapy. We demonstrated that 9-ING-41 treatment induced significant STS cells apoptosis and was synergistic in vivo when combined with chemotherapy. Mechanistically, 9-ING-41 induces significant apoptosis of STS cells via suppression of NF-κB-mediated X-linked inhibitor of apoptosis protein (XIAP) expression. These data support the inclusion of patients with STS in clinical studies of 9-ING-41 alone and in combination with chemotherapy.
【 授权许可】
Unknown