The long noncoding RNA lnc-EGFR stimulates T-regulatory cells differentiation thus promoting hepatocellular carcinoma immune evasion

被引:288
|
作者
Jiang, Runqiu [1 ,2 ]
Tang, Junwei [1 ,2 ]
Chen, Yun [3 ]
Deng, Lei [1 ,2 ]
Ji, Jie [1 ,2 ]
Xie, Yu [1 ,2 ]
Wang, Ke [1 ,2 ]
Jia, Wei [4 ]
Chu, Wen-Ming [5 ]
Sun, Beicheng [1 ,2 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Liver Transplantat Ctr, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Collaborat Innovat Ctr Canc Personalized Med, Nanjing 210029, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Dept Microbiol & Immunol, Nanjing 210029, Jiangsu, Peoples R China
[4] Univ Hawaii, Canc Ctr, Metabol Shared Resource, 701 Ilalo St, Honolulu, HI 96813 USA
[5] Univ Hawaii, Canc Ctr, Canc Biol Program, 701 Ilalo St, Honolulu, HI 96813 USA
来源
NATURE COMMUNICATIONS | 2017年 / 8卷
关键词
TUMOR-INFILTRATING LYMPHOCYTES; GROWTH-FACTOR RECEPTOR; B-VIRUS INFECTION; NF-KAPPA-B; PERIPHERAL-BLOOD; VENOUS METASTASES; OVARIAN-CANCER; LUNG-CANCER; PROGNOSIS; MICROENVIRONMENT;
D O I
10.1038/ncomms15129
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Long noncoding RNAs play a pivotal role in T-helper cell development but little is known about their roles in Treg differentiation and functions during the progression of hepatocellular carcinoma (HCC). Here, we show that lnc-epidermal growth factor receptor (EGFR) upregulation in Tregs correlates positively with the tumour size and expression of EGFR/Foxp3, but negatively with IFN-gamma expression in patients and xenografted mouse models. Lnc-EGFR stimulates Treg differentiation, suppresses CTL activity and promotes HCC growth in an EGFR-dependent manner. Mechanistically, lnc-EGFR specifically binds to EGFR and blocks its interaction with and ubiquitination by c-CBL, stabilizing it and augmenting activation of itself and its downstream AP-1/NF-AT1 axis, which in turn elicits EGFR expression. Lnc-EGFR links an immunosuppressive state to cancer by promoting Treg cell differentiation, thus offering a potential therapeutic target for HCC.
引用
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页数:15
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    Nature Communications, 8
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