Piccolo mediates EGFR signaling and acts as a prognostic biomarker in esophageal squamous cell carcinoma

被引:0
|
作者
W Zhang
R Hong
L Xue
Y Ou
X Liu
Z Zhao
W Xiao
D Dong
L Dong
M Fu
L Ma
N Lu
H Chen
Y Song
Q Zhan
机构
[1] State Key Laboratory of Molecular Oncology,Department of Pathology
[2] Cancer Institute and Cancer Hospital,Department of Neurosurgery
[3] Chinese Academy of Medical Sciences and Peking Union Medical College,undefined
[4] Collaborative Innovation Center for Biotherapy,undefined
[5] West China Hospital,undefined
[6] Sichuan University,undefined
[7] Guangdong Koheala Precision Medicine Institute,undefined
[8] Sun Yat-Sen University Cancer Center,undefined
[9] State Key Laboratory of Oncology in South China,undefined
[10] Collaborative Innovation Center of Cancer Medicine,undefined
[11] Cancer Institute and Cancer Hospital,undefined
[12] Peking Union Medical College and Chinese Academy of Medical Sciences,undefined
[13] Tiantan Hospital,undefined
[14] Capital Medical University,undefined
[15] Institute of Cancer Stem Cell,undefined
[16] Cancer Center,undefined
[17] Dalian Medical University,undefined
[18] Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education),undefined
[19] Peking University Cancer Hospital & Institute,undefined
来源
Oncogene | 2017年 / 36卷
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摘要
The presynaptic cytomatrix protein Piccolo, encoded by PCLO, is frequently mutated and amplified in esophageal squamous cell carcinoma (ESCC), but its exact roles in ESCC remain unclear. Here we report that Piccolo expression correlates significantly with clinical stage, patient survival and tumor embolus. Functional studies demonstrate that PCLO knockdown remarkably attenuates ESCC malignancy in vitro and in vivo, and ectopic EGFR expression partially compensates for Piccolo loss. PCLO knockdown promotes ubiquitination and degradation of EGFR, which is associated with the negative regulatory effect of Piccolo on E3 ligase Siah1. An anti-Piccolo monoclonal antibody inhibited tumor proliferation in a mouse model of ESCC. These results demonstrate that Piccolo contributes to tumor aggressiveness in ESCC, likely by stabilizing EGFR and promoting EGFR-dependent signaling. Our results further suggest that Piccolo may represent a novel prognostic biomarker and therapeutic target for patients with ESCC.
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页码:3890 / 3902
页数:12
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