Prognostic Value of Phosphotyrosine Phosphatases in Hepatocellular Carcinoma

被引:22
|
作者
Zhangyuan, Guangyan [1 ,2 ]
Yin, Yin [1 ,2 ]
Zhang, Wenjie [3 ,4 ]
Yu, WeiWei [1 ,2 ]
Jin, Kangpeng [1 ,2 ]
Wang, Fei [1 ,2 ]
Huang, Ruyi [1 ,2 ]
Shen, Haiyuan [1 ,2 ]
Wang, Xiaochen [1 ,2 ]
Sun, Beicheng [1 ,2 ,3 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Liver Transplantat Ctr, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Dept Hepatobilliary Surg, Drum Tower Clin Med Coll, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Dept Hepatobilliary Surg, Affiliated Drum Tower Hosp, Sch Med, Nanjing, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Dept Gen Surg, Affiliated Hosp 1, Nanjing, Jiangsu, Peoples R China
关键词
Hepatocellular carcinoma; TCGA; Phosphotyrosine phosphatase; Cancer specific survival; PROTEIN-TYROSINE PHOSPHATASES; HEPATITIS-B-VIRUS; TUMOR-SUPPRESSOR; BREAST-CANCER; LIVER-CANCER; PTPN12; EPIDEMIOLOGY; BIOMARKER; RESECTION; CELLS;
D O I
10.1159/000489625
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background/Aims: During the occurrence and progression of hepatocellular carcinoma (HCC), phosphotyrosine phosphatases (PTPs) are usually described as tumor suppressors or proto-oncogenes, and to some degree are correlated with the prognosis of HCC. Methods: A total of 321 patients from the Cancer Genome Atlas (TCGA) database and 180 patients from our validated cohort with hepatocellular carcinoma were recruited in this study. Kaplan-Meier, univariate and multivariate Cox proportional hazards model were used to evaluate the risk factors for survival. Quantitative real-time PCR (qRT-PCR) and immunohistochemistry (IHC) were applied to detect the expression levels of PTP genes. Results: After screening the data of TCGA, we identified five PTPs as HCC overall survival related PTP genes, among which only three (PTPN12, PTPRN, PTPN18) exhibited differential expression levels in our 180 paired HCC and adjacent tissues (P< 0.001). Further analysis revealed that expression of PTPN18 was positively, but PTPRN was negatively associated with prognosis of HCC both in TCGA cohort and our own cohort. As to PTPN12, results turned out to be opposite according to HBV status. In detail, higher expression of PTPN12 was associated with better outcome in HBV group but worse prognosis in Non-HBV group. Conclusion: Our results suggested that PTPN12, PTPRN and PTPN18 were independent prognostic factors in HCC. (C) 2018 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:2335 / 2346
页数:12
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