Evidence map›Paper›PMID 30103712›Full record

ArticleBMC cancer2018

Hornerin promotes tumor progression and is associated with poor prognosis in hepatocellular carcinoma.

Shun-Jun Fu, Shun-Li Shen, Shao-Qiang Li, Yun-Peng Hua, Wen-Jie Hu, BeiChu Guo, Bao-Gang Peng

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

21 citing papers in PubMed, 42 citations in OpenAlex.

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  17. CDKN1A/p21American journal of cancer research · 2021
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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 4 institutions in 2 countries.

Shun-Jun FuDepartment of Liver Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Shun-Li ShenDepartment of Liver Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Shao-Qiang LiDepartment of Liver Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Yun-Peng HuaDepartment of Liver Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
Wen-Jie HuDepartment of Liver Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China.
BeiChu GuoDepartment of Microbiology and Immunology, Hollings Cancer Center, Medical University of South Carolina, Charleston, 29425, USA. guobe@musc.edu.
Bao-Gang PengDepartment of Liver Surgery, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510080, China. pengbaogang1963@163.com.
The First Affiliated Hospital, Sun Yat-sen University · CNSun Yat-sen University · CNMedical University of South Carolina · USSouthern Medical University · CN

Funding

the China Postdoctoral Science Foundation 2015M582474the National Natural Science Foundation of China 81702313the Natural Science of Guangdong Province 2016A030310177the Science and Technology Project of Guangdong Province 2016A020215184
6 · The paper itself

Abstract

backgroundThe function of hornerin (HRNR), a member of the S100 protein family, is poorly clarified in the development of human tumors. The role of HRNR in hepatocellular carcinoma (HCC) progression is investigated in the study.

methodsThe expression levels of HRNR were assessed in tumor samples from a cohort of 271 HCC patients. The effect of HRNR on proliferation, colony formation and invasion of tumor cells was examined. We further determined the role of HRNR in tumor growth in vivo by using xenograft HCC tumor models. The possible mechanism of the HRNR promotion of HCC progression was explored.

resultsWe found that HRNR was overexpressed in HCC tissues. The high expression of HRNR in HCCs was significantly associated with vascular invasion, poor tumor differentiation, and advanced TNM stage. The disease-free survival (DFS) and overall survival (OS) of HCC patients with high HRNR expression were poorer than those in the low HRNR expression group. HRNR expression was an independent risk factor linked to both poor DFS (HR = 2.209, 95% CI = 1.627-2.998,P <  0.001) and OS (HR = 2.459,95% CI = 1.736-3.484, P <  0.001). In addition, the knockdown of HRNR by shRNAs significantly inhibited the proliferation, colony formation, migration and invasion of HCC tumor cells. HRNR silencing led to the decreased phosphorylation of AKT signaling. Notably, tumor growth was markedly inhibited by HRNR silencing in a xenograft model of HCC.

conclusionsHRNR promotes tumor progression and is correlated with a poor HCC prognosis. HRNR may contribute to HCC progression via the regulation of the AKT pathway.

Indexed as

AdultAgedAnimalsCalcium-Binding ProteinsCarcinoma, HepatocellularCell MovementCell ProliferationDisease-Free SurvivalDisease ProgressionDNA MethylationFemaleGene Expression Regulation, NeoplasticHumansIntermediate Filament ProteinsLiver NeoplasmsMaleCalcium-Binding ProteinsHRNR protein, humanIntermediate Filament ProteinsOncogene Protein v-aktAKTHepatocellular carcinomaHornerinPrognosisTumor progression

Identifiers

PMID30103712
PMCPMC6090597
OpenAlexW2885392026

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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.