Evidence map›Paper›PMID 35591857›Full record

ArticleFrontiers in genetics2022

A Panel of E2F Target Gene Signature Predicting the Prognosis of Hepatocellular Carcinoma.

Wenmin Hu, Yongmei Shi, Tongqin Han, Caiyun Liu, Xipeng Cao, Guangjun Shi, Wenjing Zhu

Abstract read
In one paragraph

Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

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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.

Wenmin HuSchool of Medicine and Pharmacy, Ocean University of China, Department of Pulmonary and Critical Care Medicine, Qingdao Municipal Hospital, Qingdao, China.
Yongmei ShiDepartment of Gynecology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, Qingdao, China.
Tongqin HanDepartment of General Practice, Qingdao Municipal Hospital, School of Medicine, Qingdao University, Qingdao, China.
Caiyun LiuDepartment of Hepatobiliary Surgery, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
Xipeng CaoClinical Research Center, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
Guangjun ShiDepartment of Hepatobiliary Surgery, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.
Wenjing ZhuClinical Research Center, Qingdao Municipal Hospital, Qingdao University, Qingdao, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma is one of the most malignant tumors, and the therapeutic effects of traditional treatments are poor. It is urgent to explore and identify new biomarkers and therapeutic targets to develop novel treatments which are individualized and effective. Three hallmarks, including E2F targets, G2M checkpoint and DNA repair, were collected by GSEA analysis. The panel of E2F-related gene signature consisted of five genes: HN1, KIF4A, CDCA3, CDCA8 and SSRP1. They had various mutation rates ranging from 0.8 to 5% in hepatocellular carcinoma, and patients with gene mutation had poorer prognosis. Among these genes, HN1 has the greatest mutation rate, and SSRP1 has the greatest impact on the model with a B (COX) value of 0.8842. Patients with higher expression of these genes had poorer prognosis. Kaplan-Meier curves in stratified survival analysis confirmed that patients with high risk scores had poor prognosis (

Indexed as

E2F target genegene signaturehepatocellular carcinomaprognosisrisk

Identifiers

PMID35591857
PMCPMC9110819

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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.