Evidence map›Paper›PMID 35774357›Full record

ArticleJournal of oncology2022

The Landscape of Using Glycosyltransferase Gene Signatures for Overall Survival Prediction in Hepatocellular Carcinoma.

Qiang Cai, Shizhe Yu, Jian Zhao, Duo Ma, Long Jiang, Xinyi Zhang, Zhiyong Yu

Open access · hybridAbstract read
In one paragraph

Article in Journal of oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 94% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 2 institutions in 1 country.

Qiang CaiDepartment of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Yunnan University, Kunming 650021, China.
Shizhe YuDepartment Surgery, First Affiliated Hospital of Zhengzhou University, Zhengzhou 400052, China.
Jian ZhaoDepartment of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Yunnan University, Kunming 650021, China.
Duo MaDepartment of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Yunnan University, Kunming 650021, China.
Long JiangDepartment of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Yunnan University, Kunming 650021, China.
Xinyi ZhangDepartment of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Yunnan University, Kunming 650021, China.
Zhiyong YuDepartment of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Yunnan University, Kunming 650021, China.ORCID https://orcid.org/0000-0002-6780-7875
Yunnan University · CNFirst Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a heterogeneous disease that occurs in the setting of chronic liver diseases. The role of glycosyltransferase (GT) genes has recently been the focus of research associated with tumor development. However, the prognostic value of GT genes in HCC remains unclear. Therefore, this study aimed to identify GT genes related to HCC prognosis through bioinformatics analysis. We firstly constructed a prognostic signature based on four GT genes using univariate and least absolute shrinkage and selection operator (LASSO) Cox regression analyses in The Cancer Genome Atlas (TCGA) dataset. Next, the risk score of each patient was calculated, and HCC patients were divided into high- and low-risk groups. Kaplan-Meier analysis showed that the survival rate of high-risk patients was significantly lower than that of low-risk patients. Receiver operating characteristic (ROC) curves assessed that risk scores calculated with a four-gene signature could predict 3- and 5-year overall survival (OS) of HCC patients, revealing the prognostic ability of this gene signature. Moreover, univariate and multivariate Cox regression analyses demonstrated that the risk score was an independent prognostic factor of HCC. Finally, functional analysis revealed that immune-related pathways were enriched and the immune status was different between the two risk groups in HCC. In summary, the novel GT gene signature could be used for prognostic prediction of HCC. Thus, targeting the GT genes may serve as an alternative treatment strategy for HCC.

Identifiers

PMID35774357
PMCPMC9239767
OpenAlexW4283384512

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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.