Cheng Hui, Chen Li, Huang Chongmei
Department of Hematology, First Affiliated Hospital, Naval Medical University, Shanghai 200433, P.R. China.
Department of Hematology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200080, P.R. China.
Oncol Lett. 2025 Jan 8;29(3):134. doi: 10.3892/ol.2025.14881. eCollection 2025 Mar.
Signal transducer and activator of transcription 3 (STAT3), a crucial transcription factor, exerts a notable influence by hyperactivating or acquiring functional mutations in the occurrence and progression of cancers. Hyperactive STAT3 is also implicated in a range of hematopoietic malignancies, especially acute myeloid leukemia (AML). The function of STAT3 is associated with the phosphorylated parallel dimer structure, enabling them to stimulate the transcription of specific genes. AML is a highly heterogeneous hematological malignancy, which is challenging in terms of therapy. The current efficacy of chemotherapy and targeted therapy remains suboptimal. Targeted inhibition of STAT3 has the potential to enhance the efficacy of AML treatment, thereby possibly improving the prognosis of individuals suffering from AML. The present review summarizes the development of inhibitors against STAT3 and discusses their applicability as AML therapeutics, which could inspire new possibilities for enhancing AML treatment strategies.
信号转导与转录激活因子3(STAT3)是一种关键的转录因子,在癌症的发生和发展过程中,通过过度激活或获得功能突变发挥显著影响。过度活跃的STAT3也与一系列血液系统恶性肿瘤有关,尤其是急性髓系白血病(AML)。STAT3的功能与磷酸化的平行二聚体结构相关,使其能够刺激特定基因的转录。AML是一种高度异质性的血液系统恶性肿瘤,在治疗方面具有挑战性。目前化疗和靶向治疗的疗效仍不理想。对STAT3进行靶向抑制有可能提高AML的治疗效果,从而可能改善AML患者的预后。本综述总结了针对STAT3的抑制剂的发展情况,并讨论了它们作为AML治疗药物的适用性,这可能为增强AML治疗策略带来新的可能性。