Evidence map›Paper›PMID 36474267›Full record

ArticleInfectious agents and cancer2022

Construction and validation of prognostic signature for hepatocellular carcinoma basing on hepatitis B virus related specific genes.

Lei Wang, Manman Qiu, Lili Wu, Zexing Li, Xinyi Meng, Lu He, Bing Yang

Open access · goldAbstract read
In one paragraph

Article in Infectious agents and cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 22 citations in OpenAlex.

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  8. The role and therapeutic value of NUSAP1 in human cancers.Journal of translational medicine · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 1 country.

Lei Wang *Tianjin Second People's Hospital, Tianjin, 300192, China.
Manman Qiu *College of Life Sciences, Nankai University, Tianjin, 300071, China.
Lili WuLogistics University of People's Armed Police Force, Tianjin, 300000, China.
Zexing LiSchool of Life Sciences, Tianjin University, Tianjin, 300072, China.
Xinyi MengDepartment of Cell Biolopgy, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China.
Lu HeDepartment of Anatomy and Histology, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China.
Bing YangDepartment of Cell Biolopgy, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, 300070, China. bingyang@tmu.edu.cn.
Tianjin Medical University · CNLogistics University of People's Armed Police Force · CNNankai University · CNTianjin University · CNTianjin Vocational Institute · CN

Funding

Educational Committee Foundation of Tianjin City 2020KJ196Foundation of Logistics University of People's Armed Police Force WHJ202111Tianjin Natural Science Foundation 19JCQNJC08700
6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is a frequent primary liver cancer, and it is one of the leading cause of cancer-related deaths. Hepatitis B virus (HBV) infection is a crucial risk factor for HCC. Thus, this study aimed to explore the prognostic role of HBV-positive HCC related specific genes in HCC.

methodsThe HCC related data were downloaded from three databases, including The Cancer Genome Atlas (TCGA), International Cancer Genome Consortium (ICGC), and Gene Expression Omnibus (GEO). Univariate Cox regression analysis and LASSO Cox regression analysis were conducted to build the Risk score. Multivariate Cox regression analysis and survival analysis determined the independent prognostic indicators.

resultsAfter cross analysis of differentially expressed genes (DEGs), we have identified 106 overlapped DEGs, which were probably HBV-positive HCC related specific genes. These 106 DEGs were significantly enriched in 213 GO terms and 8 KEGG pathways. Among that, 11 optimal genes were selected to build a Risk score, and Risk score was an independent prognostic factor for HCC. High risk HCC patients had worse OS. Moreover, five kinds of immune cells were differentially infiltrated between high and low risk HCC patients.

conclusionThe prognostic signature, based on HMMR, MCM6, TPX2, KIF20A, CCL20, RGS2, NUSAP1, FABP5, FZD6, PBK, and STK39, is conducive to distinguish different prognosis of HCC patients.

Indexed as

Hepatitis B virus (HBV)Hepatocellular carcinoma (HCC)Overall survivalPrognostic signature

Identifiers

PMID36474267
PMCPMC9727957
OpenAlexW4310948043

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.