Zhao Yahui, Luo Aiping, Li Sheng, Zhang Wei, Chen Hongyan, Li Yi, Ding Fang, Huang Furong, Liu Zhihua
From the State Key Laboratory of Molecular Oncology, Cancer Institute and Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Collaborative Innovation Center for Cancer Medicine, Beijing 100021, China and.
the Department of Cell Biology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Center for Molecular and Translational Medicine, Peking University Cancer Hospital and Institute, Beijing 100142, China.
J Biol Chem. 2016 Mar 25;291(13):6831-42. doi: 10.1074/jbc.M115.704361. Epub 2016 Feb 8.
ID1 (inhibitor of differentiation/DNA binding 1) acts an important role in metastasis, tumorigenesis, and maintenance of cell viability. It has been shown that the up-regulation of ID1 is correlated with poor prognosis and the resistance to chemotherapy of human cancers. However, the underlying molecular mechanism remains elusive. Here, we determined for the first time that up-regulating ID1 upon etoposide activation was mediated through AP-1 binding sites within theID1promoter and confirmed that ID1 enhanced cell resistance to DNA damage-induced apoptosis in esophageal squamous cell carcinoma cells. Ablation of c-Jun/c-Fos or ID1 expression enhanced etoposide-mediated apoptosis through increasing activity of caspase 3 and PARP cleavage. Moreover, c-Jun/c-Fos and ID1 were positively correlated in human cancers. More importantly, simultaneous high expression of ID1 and c-Jun or c-Fos was correlated with poor survival in cancer patients. Collectively, we demonstrate the importance of c-Jun/c-Fos-ID1 signaling pathway in chemoresistance of esophageal cancer cells and provide considerable insight into understanding the underlying molecular mechanisms in esophageal squamous cell carcinoma cell biology.
ID1(分化/DNA结合抑制因子1)在转移、肿瘤发生及细胞活力维持过程中发挥重要作用。研究表明,ID1的上调与人类癌症的不良预后及化疗耐药性相关。然而,其潜在分子机制仍不清楚。在此,我们首次确定依托泊苷激活后ID1的上调是通过ID1启动子内的AP-1结合位点介导的,并证实ID1增强了食管鳞状细胞癌细胞对DNA损伤诱导凋亡的抗性。敲除c-Jun/c-Fos或ID1表达通过增加半胱天冬酶3的活性和聚(ADP-核糖)聚合酶的切割来增强依托泊苷介导的凋亡。此外,c-Jun/c-Fos与ID1在人类癌症中呈正相关。更重要的是,ID1与c-Jun或c-Fos同时高表达与癌症患者的不良生存相关。总体而言,我们证明了c-Jun/c-Fos-ID1信号通路在食管癌细胞化疗耐药中的重要性,并为理解食管鳞状细胞癌细胞生物学的潜在分子机制提供了深入见解。