共 50 条
N-myc downstream-regulated gene 1 promotes apoptosis in colorectal cancer via up-regulating death receptor 4
被引:13
|作者:
Zhang, Xian
[1
,2
,3
]
Feng, Bo
[3
]
Zhu, Fan
[3
]
Yu, Chaoran
[3
]
Lu, Jiaoyang
[3
]
Pan, Meng
[3
]
He, Zirui
[3
]
Wangpu, Xiongzhi
[3
]
Sun, Jing
[3
]
Yang, Xiao
[1
,2
]
机构:
[1] Shanghai Jiao Tong Univ, Shanghai Inst Digest Surg, Ruijin Hosp, Sch Med, Shanghai 200025, Peoples R China
[2] Tongji Univ, Shanghai East Hosp, Div Gastrointestinal & Colorectal Surg, Dept Gen Surg, Shanghai 200120, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Dept Gen Surg, Ruijin Hosp, Shanghai 200025, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
apoptosis;
colorectal cancer;
death receptor;
NDRG1;
TRAIL;
TRAIL-INDUCED APOPTOSIS;
METASTASIS SUPPRESSOR;
DOWN-REGULATION;
NDRG1;
PROLIFERATION;
CELLS;
EXPRESSION;
MIGRATION;
PROTEINS;
INVASION;
D O I:
10.18632/oncotarget.19658
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
The aim of this study was to evaluate the clinical significance of N-myc downstream-regulated gene 1 (NDRG1) in colorectal cancer (CRC) patients and to explore the mechanisms governing the role of NDRG1 in apoptosis of CRC cells. In the current study, we found that NDRG1 was a prognostic marker of CRC patients. Moreover, NDRG1 expression negatively correlated to tumor size and clinical TNM stage, suggesting that NDRG1 might act as a tumor suppressor by inhibiting proliferation or inducing apoptosis in CRC. Consistently, substantial apoptosis was observed in vitro and in vivo in the presence of NDRG1. From a mechanistic standpoint, we discovered that NDRG1 was able to prevent death receptor 4 from degradation induced by MARCH-8, a member of the membrane-associated RING-CH (MARCH) ubiquitin ligase family. As a consequence, CRC cells expressing NDRG1 were more sensitive to reagents targeting death receptors such as tumor necrosis factor-related apoptosis-inducing ligands (TRAIL). Additionally, the pro-apoptotic effect of NDRG1 was also validated in mouse xenograft model. In conclusion, our results provided further insights of the pivotal role of NDRG1 in apoptosis initiated by death receptors and demonstrated a novel marker to predict the sensitivity of CRC to TRAIL treatment in future clinical study.
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页码:82593 / 82608
页数:16
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