Hu Jiaru, Meng Fang, Lv Lei, Hong Fu, He Qing, Zhu Qi, Tian Tian, Chang Na, Zhang Shiqiang, Yi Qiyi, Qian Liting
Department of Radiation Oncology, Anhui Provincial Cancer Hospital, the First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230001, China.
Department of Oncology & Hematology, Xishan People's Hospital of Wuxi City, Wuxi, 214105, China.
Cell Death Dis. 2024 Dec 27;15(12):933. doi: 10.1038/s41419-024-07240-1.
Radiotherapy resistance is one of the main reasons for the dismal clinical outcome of patients with esophageal squamous cell carcinoma (ESCC). Therefore, clarifying the targets and molecular mechanisms of radiotherapy resistance in ESCC is of great theoretical and clinical significance to enhance the efficacy of radiotherapy. In this study, GPR37 was identified as a key factor facilitating ESCC radiosensitization. We found that GPR37 is lowly expressed in ESCC, especially in radioresistant ESCC tumors. And its insufficiency is related to the malignant characteristics and unfavorable prognosis in ESCC. Further investigation revealed that GPR37 level is inversely regulated by promoter methylation but positively regulated by ZNF750. Functionally, GPR37 could not only overcome radioresistance of ESCC, but also inhibit proliferation, migration, and invasion. Mechanistically, GPR37 interacts with the ATP1A1 protein, effectively promoting its ubiquitination-induced degradation, thereby limiting the activation of the AKT/mTOR signaling pathway. Additionally, GPR37 can be transported to recipient cells via exosomes and inhibit the malignant behavior of recipient cells. Overall, these findings suggest that GPR37-ATP1A1 axis holds potential as a therapeutic target for the management of ESCC, especially for overcoming radiation resistance.
放射治疗抵抗是食管鳞状细胞癌(ESCC)患者临床结局不佳的主要原因之一。因此,阐明ESCC放射治疗抵抗的靶点和分子机制对于提高放射治疗疗效具有重要的理论和临床意义。在本研究中,GPR37被确定为促进ESCC放射增敏的关键因素。我们发现GPR37在ESCC中低表达,尤其是在放射抵抗的ESCC肿瘤中。其表达不足与ESCC的恶性特征和不良预后相关。进一步研究表明,GPR37水平受启动子甲基化的负调控,但受ZNF750的正调控。在功能上,GPR37不仅可以克服ESCC的放射抵抗,还可以抑制其增殖、迁移和侵袭。机制上,GPR37与ATP1A1蛋白相互作用,有效促进其泛素化诱导的降解,从而限制AKT/mTOR信号通路的激活。此外,GPR37可以通过外泌体转运至受体细胞并抑制受体细胞的恶性行为。总体而言,这些发现表明GPR37-ATP1A1轴有望成为ESCC治疗的靶点,尤其是在克服放射抵抗方面。