Li Pengpeng, Chu Dan, Ding Guangcheng, Qin Dehua, Bu Yajing, Tian Bi
Tumor Treatment Center, The Fifth Affiliated Hospital of Zhengzhou University, No. 3 Kangfuqian Street, Erqi District, Zhengzhou, 450052, China.
Department of Respiratory Medicine, The First Affiliated Hospital of Zhengzhou University, No. 1 Jianshe East Road, Erqi District, Zhengzhou, 450052, China.
Mol Cell Biochem. 2025 Apr;480(4):2361-2375. doi: 10.1007/s11010-024-05068-z. Epub 2024 Jul 18.
Ferroptosis is recently discovered as an important player in the initiation, proliferation, and progression of human tumors. Insulin-like growth factor 2 mRNA-binding protein 3 (IGF2BP3) has been reported as an oncogene in multiple types of cancers, including lung adenocarcinoma (LUAD). However, little research has been designed to investigate the regulation of IGF2BP3 on ferroptosis in LUAD. qRT-PCR and western blot were used to measure the mRNA and protein expression of IGF2BP3 and transcription factor AP-2 alpha (TFAP2A). CCK-8 assay was performed to determine cell viability. DCFH-DA and C11-BODIPY staining were used to detect the levels of intracellular reactive oxygen species (ROS) and lipid ROS. The corresponding assay kits were used to analyze the levels of malondialdehyde (MDA) and glutathione (GSH). SRAMP website and m6A RNA immunoprecipitation (Me-RIP) were used to predict and confirm the m6A modification of TFAP2A. RIP experiments were conducted to confirm the binding of IGF2BP3 and TFAP2A. RNA stability assay was performed using actinomycin D. Chromatin immunoprecipitation (ChIP) and dual-luciferase reporter experiments were performed to confirm the interaction between TFAP2A and cystine/glutamate antiporter solute carrier family 7 member 11 (SLC7A11) or glutathione peroxidase 4 (GPX4). Mice xenotransplant model was also constructed to explore the effect of IGF2BP3 on LUAD tumor growth and ferroptosis. IGF2BP3 and TFAP2A were both highly expressed in LUAD. IGF2BP3 or TFAP2A knockdown induced ferroptosis by aggravating erastin-induced cell viability suppression, increasing the production of intracellular ROS, lipid ROS, and MDA, and decreasing GSH synthesis, GSH/GSSG ratio, and cystine uptake. Mechanistically, IGF2BP3 stabilized TFAP2A expression via m6A modification. Moreover, sh-IGF2BP3-mediated ferroptosis was significantly abated by TFAP2A overexpression. Furthermore, TFAP2A binds to the promoters of SLC7A11 and GPX4 to promote their transcription. Also, IGF2BP3 depletion suppressed LUAD tumor growth by inducing ferroptosis in mice. IGF2BP3 suppresses ferroptosis in LUAD by m6A-dependent regulation of TFAP2A to promote the transcription of SLC7A11 and GPX4. Our findings suggest that targeting IGF2BP3/TFAP2A/SLC7A11/GPX4 axis might be a potential therapeutic choice to increase ferroptosis sensitivity in LUAD.
铁死亡最近被发现是人类肿瘤发生、增殖和进展中的一个重要因素。胰岛素样生长因子2 mRNA结合蛋白3(IGF2BP3)在包括肺腺癌(LUAD)在内的多种癌症中被报道为一种癌基因。然而,很少有研究旨在探究IGF2BP3对LUAD中铁死亡的调控作用。采用qRT-PCR和蛋白质免疫印迹法检测IGF2BP3和转录因子AP-2α(TFAP2A)的mRNA和蛋白质表达。进行CCK-8检测以确定细胞活力。采用DCFH-DA和C11-BODIPY染色检测细胞内活性氧(ROS)和脂质ROS水平。使用相应的检测试剂盒分析丙二醛(MDA)和谷胱甘肽(GSH)水平。利用SRAMP网站和m6A RNA免疫沉淀(Me-RIP)预测并确认TFAP2A的m6A修饰。进行RNA免疫沉淀(RIP)实验以确认IGF2BP3与TFAP2A的结合。使用放线菌素D进行RNA稳定性检测。进行染色质免疫沉淀(ChIP)和双荧光素酶报告基因实验以确认TFAP2A与胱氨酸/谷氨酸反向转运体溶质载体家族7成员11(SLC7A11)或谷胱甘肽过氧化物酶4(GPX4)之间的相互作用。还构建了小鼠异种移植模型以探究IGF2BP3对LUAD肿瘤生长和铁死亡的影响。IGF2BP3和TFAP2A在LUAD中均高表达。敲低IGF2BP3或TFAP2A可通过加重埃拉斯汀诱导的细胞活力抑制、增加细胞内ROS、脂质ROS和MDA的产生以及降低GSH合成、GSH/GSSG比值和胱氨酸摄取来诱导铁死亡。机制上,IGF2BP3通过m6A修饰稳定TFAP2A的表达。此外,TFAP2A过表达可显著减轻sh-IGF2BP3介导的铁死亡。此外,TFAP2A与SLC7A11和GPX4的启动子结合以促进它们的转录。而且,IGF2BP3缺失通过诱导小鼠铁死亡抑制LUAD肿瘤生长。IGF2BP3通过对TFAP2A的m6A依赖性调控促进SLC7A11和GPX4的转录,从而抑制LUAD中的铁死亡。我们的研究结果表明,靶向IGF2BP3/TFAP2A/SLC7A11/GPX4轴可能是提高LUAD中铁死亡敏感性的一种潜在治疗选择。