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Competitive Binding Between Id1 and E2F1 to Cdc20 Regulates E2F1 Degradation and Thymidylate Synthase Expression to Promote Esophageal Cancer Chemoresistance.Id1与E2F1对Cdc20的竞争性结合调节E2F1降解及胸苷酸合成酶表达以促进食管癌化疗耐药
Clin Cancer Res. 2016 Mar 1;22(5):1243-55. doi: 10.1158/1078-0432.CCR-15-1196. Epub 2015 Oct 16.
2
Integrative transcriptomics-based identification of cryptic drivers of taxol-resistance genes in ovarian carcinoma cells: Analysis of the androgen receptor.基于整合转录组学鉴定卵巢癌细胞中紫杉醇耐药基因的隐匿驱动因素:雄激素受体分析
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Stemness and chemotherapeutic drug resistance induced by EIF5A2 overexpression in esophageal squamous cell carcinoma.EIF5A2过表达诱导食管鳞状细胞癌的干性及化疗耐药性。
Oncotarget. 2015 Sep 22;6(28):26079-89. doi: 10.18632/oncotarget.4581.
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Establishment and characterization of cetuximab resistant head and neck squamous cell carcinoma cell lines: focus on the contribution of the AP-1 transcription factor.建立并鉴定西妥昔单抗耐药的头颈部鳞状细胞癌细胞系:重点关注 AP-1 转录因子的作用。
Am J Cancer Res. 2015 May 15;5(6):1921-38. eCollection 2015.
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LIF negatively regulates tumour-suppressor p53 through Stat3/ID1/MDM2 in colorectal cancers.白血病抑制因子通过Stat3/ID1/MDM2在结直肠癌中对肿瘤抑制因子p53起负调控作用。
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Id proteins: small molecules, mighty regulators.Id 蛋白:小分子,大调节。
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分化抑制因子/DNA结合蛋白1(ID1)以c-Jun/c-Fos依赖的方式抑制依托泊苷诱导的细胞凋亡。

Inhibitor of Differentiation/DNA Binding 1 (ID1) Inhibits Etoposide-induced Apoptosis in a c-Jun/c-Fos-dependent Manner.

作者信息

Zhao Yahui, Luo Aiping, Li Sheng, Zhang Wei, Chen Hongyan, Li Yi, Ding Fang, Huang Furong, Liu Zhihua

机构信息

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.

出版信息

J Biol Chem. 2016 Mar 25;291(13):6831-42. doi: 10.1074/jbc.M115.704361. Epub 2016 Feb 8.

DOI:10.1074/jbc.M115.704361
PMID:26858249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4807270/
Abstract

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.

摘要

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。