Department of Radiation Oncology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Department of Pathology, Nanfang Hospital and Basic Medical College, Southern Medical University, Guangzhou, Guangdong, China; Department of Pathology, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China; Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, Guangdong, China.
J Hepatol. 2022 May;76(5):1138-1150. doi: 10.1016/j.jhep.2022.01.009. Epub 2022 Jan 29.
BACKGROUND & AIMS: Copper (Cu) is an essential trace element whose serum levels have been reported to act as an effective indicator of the efficacy of radiotherapy. However, little is known about the role of Cu in radiotherapy. In this study we aimed to determine this role and investigate the precise mechanism by which Cu or Cu-related proteins regulate the radiosensitivity of hepatocellular carcinoma (HCC).
The expression and function of Cu and copper metabolism MURR1 domain 10 (COMMD10) were assessed via a Cu detection assay, immunostaining, real-time PCR, western blot, a radiation clonogenic assay and a 5-ethynyl-2'-deoxyuridine assay. Ferroptosis was determined by detecting glutathione, lipid peroxidation, malondialdehyde and ferrous ion (Fe) levels. The in vivo effects of Cu and COMMD10 were examined with Cu/Cu chelator treatment or lentivirus modification of COMMD10 expression in radiated mouse models.
We identified a novel role of Cu in promoting the radioresistance of HCC cells. Ionizing radiation (IR) induced a reduction of COMMD10, which increased intracellular Cu and led to radioresistance of HCC. COMMD10 enhanced ferroptosis and radiosensitivity in vitro and in vivo. Mechanistically, low expression of COMMD10 induced by IR inhibited the ubiquitin degradation of HIF1α (by inducing Cu accumulation) and simultaneously impaired its combination with HIF1α, promoting HIF1α nuclear translocation and the transcription of ceruloplasmin (CP) and SLC7A11, which jointly inhibited ferroptosis in HCC cells. In addition, elevated CP promoted HIF1α expression by reducing Fe, forming a positive feedback loop.
COMMD10 inhibits the HIF1α/CP loop to enhance ferroptosis and radiosensitivity by disrupting Cu-Fe homeostasis in HCC. This work provides new targets and treatment strategies for overcoming radioresistance in HCC.
Radiotherapy benefits patients with unresectable or advanced hepatocellular carcinoma (HCC), but its effectiveness is hampered by radioresistance. Herein, we uncovered a novel role for copper in promoting the radioresistance of HCCs. This work has revealed new targets and potential treatment strategies that could be used to sensitize HCC to radiotherapy.
铜(Cu)是一种必需的微量元素,其血清水平已被报道可作为放射治疗疗效的有效指标。然而,人们对铜在放射治疗中的作用知之甚少。在本研究中,我们旨在确定这一作用,并研究铜或铜相关蛋白调节肝细胞癌(HCC)放射敏感性的确切机制。
通过铜检测、免疫染色、实时 PCR、western blot、放射集落形成测定和 5-乙炔基-2'-脱氧尿苷测定评估铜和铜代谢 MURR1 结构域 10(COMMD10)的表达和功能。通过检测谷胱甘肽、脂质过氧化、丙二醛和亚铁离子(Fe)水平来确定铁死亡。用铜/铜螯合剂处理或慢病毒修饰 COMMD10 表达的方法,在放射小鼠模型中检测 Cu 和 COMMD10 的体内作用。
我们发现了铜在促进 HCC 细胞放射抗性中的新作用。电离辐射(IR)诱导 COMMD10 减少,从而增加细胞内铜含量,导致 HCC 放射抗性。COMMD10 增强了体外和体内的铁死亡和放射敏感性。在机制上,IR 诱导的 COMMD10 低表达通过诱导 Cu 积累抑制 HIF1α 的泛素降解,同时损害其与 HIF1α 的结合,促进 HIF1α 核转位和铜蓝蛋白(CP)和 SLC7A11 的转录,共同抑制 HCC 细胞中的铁死亡。此外,升高的 CP 通过减少 Fe 来促进 HIF1α 的表达,形成正反馈环。
COMMD10 通过破坏 HCC 中的 Cu-Fe 平衡,抑制 HIF1α/CP 环来增强铁死亡和放射敏感性。这项工作为克服 HCC 的放射抵抗提供了新的靶点和治疗策略。
放射治疗有益于不能手术或晚期肝细胞癌(HCC)患者,但放射治疗效果受到放射抵抗的限制。在此,我们揭示了铜在促进 HCC 放射抵抗中的新作用。这项工作揭示了新的靶点和潜在的治疗策略,可用于提高 HCC 对放射治疗的敏感性。