Decreased Expression of TMEM173 Predicts Poor Prognosis in Patients with Hepatocellular Carcinoma

被引:49
作者
Bu, Yang [1 ]
Liu, Fang [2 ]
Jia, Qing-An [3 ]
Yu, Song-Ning [1 ]
机构
[1] Ningxia Med Univ, Gen Hosp, Hepatobiliary Surg, Yinchuan, Peoples R China
[2] Ningxia Med Univ, Gen Hosp, Med Examinat Ctr, Yinchuan, Peoples R China
[3] Xi An Jiao Tong Univ, Affiliated Hosp 1, Hepatobiliary Surg, Xian, Peoples R China
来源
PLOS ONE | 2016年 / 11卷 / 11期
基金
中国国家自然科学基金;
关键词
CYCLIC-DI-GMP; I IFN; CANCER; SENSOR; CELLS; ACTIVATION; IMMUNITY; AMP; DNA;
D O I
10.1371/journal.pone.0165681
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
Hepatocellular carcinoma (HCC) is one of the most lethal cancer types, and chronic infection with Hepatitis B Virus (HBV) is identified as the strongest risk factor for HCC. Transmembrane Protein 173 (TMEM173) is a pattern recognition receptor which functions as a major regulator of the innate immune response to viral and bacterial infections. However, the prognostic value of TMEM173 in HCC remains elusive. Thus, we aimed to evaluate the potential prognostic significance of TMEM173 expression in HCC patients following curative resection. Immunohistochemistry was used to detect TMEM173 expression in 96 HCC patients. We found that TMEM173 protein expression was remarkably decreased in tumor tissues compared to non-tumor tissues, and that TMEM173 staining intensity was inversely correlated with tumor size, tumor invasion TNM stage and overall survival (OS) in HCC patients. Multivariate analysis supported TMEM173 as an independent prognostic factor, and identified that combining TMEM173 expression with TNM stage showed better prognostic efficiency for OS in HCC patients. In summary, TMEM173 was discovered having an independent prognostic value and may serve as a potential immunotherapeutic target for HCC.
引用
收藏
页数:11
相关论文
共 23 条
[11]  
Karimi-Googheri M, 2015, ARCH IRAN MED, V18, P351, DOI 015186/AIM.005
[12]   Novel monogenic diseases causing human autoimmunity [J].
Melkil, Isabelle ;
Crow, Yanick J. .
CURRENT OPINION IN IMMUNOLOGY, 2015, 37 :1-5
[13]   Liposomes loaded with a STING pathway ligand, cyclic di-GMP, enhance cancer immunotherapy against metastatic melanoma [J].
Nakamura, Takashi ;
Miyabe, Hiroko ;
Hyodo, Mamoru ;
Sato, Yusuke ;
Hayakawa, Yoshihiro ;
Harashima, Hideyoshi .
JOURNAL OF CONTROLLED RELEASE, 2015, 216 :149-157
[14]   Regulation of the innate immune response by threonine-phosphatase of Eyes absent [J].
Okabe, Yasutaka ;
Sano, Teruyuki ;
Nagata, Shigekazu .
NATURE, 2009, 460 (7254) :520-U99
[15]   The N-Ethyl-N-Nitrosourea-Induced Goldenticket Mouse Mutant Reveals an Essential Function of Sting in the In Vivo Interferon Response to Listeria monocytogenes and Cyclic Dinucleotides [J].
Sauer, John-Demian ;
Sotelo-Troha, Katia ;
von Moltke, Jakob ;
Monroe, Kathryn M. ;
Rae, Chris S. ;
Brubaker, Sky W. ;
Hyodo, Mamoru ;
Hayakawa, Yoshihiro ;
Woodward, Joshua J. ;
Portnoy, Daniel A. ;
Vance, Russell E. .
INFECTION AND IMMUNITY, 2011, 79 (02) :688-694
[16]   Discriminating self from non-self in nucleic acid sensing [J].
Schlee, Martin ;
Hartmann, Gunther .
NATURE REVIEWS IMMUNOLOGY, 2016, 16 (09) :566-580
[17]   Crystallization studies of the murine c-di-GMP sensor protein STING [J].
Su, Yi-Che ;
Tu, Zhi-Le ;
Yang, Chao-Yu ;
Chin, Ko-Hsin ;
Chuah, Mary Lay-Cheng ;
Liang, Zhao-Xun ;
Chou, Shan-Ho .
ACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY COMMUNICATIONS, 2012, 68 :906-910
[18]   The multifaceted biology of plasmacytoid dendritic cells [J].
Swiecki, Melissa ;
Colonna, Marco .
NATURE REVIEWS IMMUNOLOGY, 2015, 15 (08) :471-485
[19]   Agonist-Mediated Activation of STING Induces Apoptosis in Malignant B Cells [J].
Tang, Chih-Hang Anthony ;
Zundell, Joseph A. ;
Ranatunga, Sujeewa ;
Lin, Cindy ;
Nefedova, Yulia ;
Del Valle, Juan R. ;
Hu, Chih-Chi Andrew .
CANCER RESEARCH, 2016, 76 (08) :2137-2152
[20]   Neoangiogenesis-related genes are hallmarks of fast-growing hepatocellular carcinomas and worst survival. Results from a prospective study [J].
Villa, Erica ;
Critelli, Rosina ;
Lei, Barbara ;
Marzocchi, Guido ;
Camma, Calogero ;
Giannelli, Gianluigi ;
Pontisso, Patrizia ;
Cabibbo, Giuseppe ;
Enea, Marco ;
Colopi, Stefano ;
Caporali, Cristian ;
Pollicino, Teresa ;
Milosa, Fabiola ;
Karampatou, Aimilia ;
Todesca, Paola ;
Bertolini, Elena ;
Maccio, Livia ;
Luz Martinez-Chantar, Maria ;
Turola, Elena ;
Del Buono, Mariagrazia ;
De Maria, Nicola ;
Ballestri, Stefano ;
Schepis, Filippo ;
Loria, Paola ;
Gerunda, Giorgio Enrico ;
Losi, Luisa ;
Cillo, Umberto .
GUT, 2016, 65 (05) :861-869