Zhang Shanshan, Wang Haina, Zhang Xuehong, Kui Xiangjie, Huang Dan, Qin Menglu, Liu Shuqing, Sun Ming-Zhong, Yan Jinsong
Department of Hematology, Liaoning Medical Center for Hematopoietic Stem Cell Transplantation, the Second Hospital of Dalian Medical University, Dalian 116027, China.
Department of Biotechnology, College of Basic Medical Sciences, Dalian Medical University, Dalian 116044, China.
Blood Sci. 2025 Aug 11;7(3):e00246. doi: 10.1097/BS9.0000000000000246. eCollection 2025 Sep.
Due to the limited availability of effective treatment therapies, patients with refractory and relapsed acute myeloid leukemia (AML) often have poor prognoses. Therefore, identifying new therapeutic targets to improve the treatment landscape and enhance AML outcomes is critical. In this study, we demonstrated for the first time that alpha-enolase (ENO1) is markedly overexpressed in AML and is closely associated with poor prognosis. In vitro experiments revealed that ENO1 knockdown (shENO1) significantly inhibited cell proliferation and invasion, and concomitantly induced cell cycle arrest. In vivo, a mouse model engrafted with U937-shENO1 cells exhibited markedly prolonged overall survival compared with a model implanted with U937 cells. Mechanistically, ENO1 operates by activating the mitogen-activated protein kinase/extracellular signal-regulated kinase (MAPK/ERK) signaling pathway, as evidenced by the reversal of shENO1 function through ERK activation. Collectively, our findings highlight ENO1 as a promising therapeutic target in AML.
由于有效治疗方法有限,难治性和复发性急性髓系白血病(AML)患者的预后通常较差。因此,确定新的治疗靶点以改善治疗前景并提高AML治疗效果至关重要。在本研究中,我们首次证明α-烯醇化酶(ENO1)在AML中显著过表达,且与不良预后密切相关。体外实验表明,ENO1基因敲低(shENO1)显著抑制细胞增殖和侵袭,并同时诱导细胞周期停滞。在体内,与植入U937细胞的模型相比,植入U937-shENO1细胞的小鼠模型的总生存期显著延长。机制上,ENO1通过激活丝裂原活化蛋白激酶/细胞外信号调节激酶(MAPK/ERK)信号通路发挥作用,ERK激活可逆转shENO1功能证明了这一点。总之,我们的研究结果突出了ENO1作为AML中一个有前景的治疗靶点。