Evidence map›Paper›PMID 32849813›Full record

ArticleFrontiers in genetics2020

Integrated Bioinformatics Analysis Reveals Key Candidate Genes and Pathways Associated With Clinical Outcome in Hepatocellular Carcinoma.

Yubin Li, Runzhe Chen, Jian Yang, Shaowei Mo, Kelly Quek, Chung H Kok, Xiang-Dong Cheng, Saisai Tian, Weidong Zhang, Jiang-Jiang Qin

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

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  14. Network Pharmacology Integrated with Transcriptomics Deciphered the Potential Mechanism ofEvidence-based complementary and alternative medicine : eCAM · 2022
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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

10 authors at 6 institutions in 3 countries.

Yubin LiSchool of Pharmacy, Naval Medical University, Shanghai, China.
Runzhe ChenDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Jian YangSchool of Pharmacy, Naval Medical University, Shanghai, China.
Shaowei MoThe First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.
Kelly QuekDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Chung H KokPrecision Medicine Theme, South Australian Health and Medical Research Institute, Adelaide, SA, Australia.
Xiang-Dong ChengInstitute of Cancer and Basic Medicine, Chinese Academy of Sciences, Hangzhou, China.
Saisai TianSchool of Pharmacy, Naval Medical University, Shanghai, China.
Weidong ZhangSchool of Pharmacy, Naval Medical University, Shanghai, China.
Jiang-Jiang QinThe First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.
Second Military Medical University · CNThe University of Texas MD Anderson Cancer Center · USChinese Academy of Sciences · CNSouth Australian Health and Medical Research Institute · AUZhejiang Cancer Hospital · CNZhejiang Chinese Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) accounts for approximately 85-90% of all liver cancer cases and has poor relapse-free survival. There are many gene expression studies that have been performed to elucidate the genetic landscape and driver pathways leading to HCC. However, existing studies have been limited by the sample size and thus the pathogenesis of HCC is still unclear. In this study, we performed an integrated characterization using four independent datasets including 320 HCC samples and 270 normal liver tissues to identify the candidate genes and pathways in the progression of HCC. A total of 89 consistent differentially expression genes (DEGs) were identified. Gene-set enrichment analysis revealed that these genes were significantly enriched for cellular response to zinc ion in biological process group, collagen trimer in the cellular component group, extracellular matrix (ECM) structural constituent conferring tensile strength in the molecular function group, protein digestion and absorption, mineral absorption and ECM-receptor interaction. Network system biology based on the protein-protein interaction (PPI) network was also performed to identify the most connected and important genes based on our DEGs. The top five hub genes including osteopontin (

Indexed as

differentially expression genesenrichment analysishepatocellular carcinomaprognosissurvival analysis

Identifiers

PMID32849813
PMCPMC7396661
OpenAlexW3044854927

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.