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RETRACTED: Identification and Validation of an Inflammatory Response-Related Polygenic Risk Score as a Prognostic Marker in Hepatocellular Carcinoma (Retracted Article)
被引:1
|作者:
Xiaochun, Huang
[1
,2
]
Feixiong, Pang
[1
,2
]
Shengsong, Ou
[1
,2
]
Xiaojiao, Wei
[1
,2
]
Yuju, Xu
[1
,2
]
Yanhua, Lai
[1
,2
]
机构:
[1] Guangxi Acad Med Sci, Nanning, Guangxi, Peoples R China
[2] Peoples Hosp Guangxi Zhuang Autonomous Reg, Dept Transplantat, Nanning, Guangxi, Peoples R China
来源:
关键词:
ALPHA-FETOPROTEIN;
EARLY-STAGE;
LIVER;
CANCER;
METASTASIS;
CELLS;
GENES;
HSP70;
VEGFA;
D O I:
10.1155/2022/1739995
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Aims. We hypothesized that the expression patterns of inflammatory response-related genes may be a potential tool for hepatocellular carcinoma (HCC) risk scoring. Background. Inflammatory response plays a pivotal role in the pathogenesis of HCC. Objective. To establish and validate a hallmark inflammatory response gene-based polygenic risk score as a prognostic tool in HCC. Methods. We screened differentially expressed inflammatory response genes and established an inflammatory response-related polygenic risk score (IRPRS) in an HCC-related dataset. Patients with HCC were categorized into high- and low-risk groups according to the median IRPRS, and the overall survival between the two groups was compared. The IRPRS was validated in an independent external dataset. Tumor-infiltrating lymphocytes (TILs) in high- and low-risk groups were compared, and gene set enrichment analysis was performed to characterize high-risk HCC identified using this IRPRS. Results. Four differentially expressed hallmark inflammatory response genes (CD14, AQP9, SERPINE1, and ITGA5) were identified to construct the IRPRS. Patients in the high-risk group had significantly shorter overall survival than those in the low-risk group in both the training set and the test set. Furthermore, the IRPRS remained an independent prognostic factor compared to the routine clinicopathological characteristics. Many cancer-related hallmark gene sets and TILs were significantly enriched in the high-risk group. Conclusions. We established and validated a four-hallmark inflammatory response gene-based polygenic risk score, which could successfully divide patients with HCC into high-risk and low-risk groups. These two risk groups of HCC possess significantly distinct prognostic and biological characteristics.
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