Evidence map›Paper›PMID 35576868›Full record

ArticleClinics (Sao Paulo, Brazil)2022

CLEC14A was up-regulated in hepatocellular carcinoma and may function as a potential diagnostic biomarker.

Lang Yan, Xiang Li, Yunfeng Yuan

Open access · goldAbstract read
In one paragraph

Article in Clinics (Sao Paulo, Brazil), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 48% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. A novel methylation marker on theFrontiers in oncology · 2026
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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

3 authors at 1 institution in 1 country.

Lang YanChongqing University Three Gorges Hospital, Chongqing, China.
Xiang LiChongqing University Three Gorges Hospital, Chongqing, China.
Yunfeng YuanChongqing University Three Gorges Hospital, Chongqing, China. Electronic address: yyf666180@hotmail.com.
Chongqing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe current work aimed to investigate the expression and potential clinical significance of C-type Lectin domain family 14 (CLEC14A) in hepatocellular carcinoma.

methodsThe relative expressions of CLEC14A in the Hepatocellular Carcinoma (HCC) tissue and adjacent normal tissue of 105 HCC patients were examined using RT-qPCR methods. Furthermore, Receiver Operating Characteristic (ROC) curve was drawn for exploring the diagnostic value of CLEC14A. Next, the expressions of CLEC14A in HCC cell lines and normal liver epithelial cells were compared, and the effects of knockdown of CLEC14A on the growth and apoptosis of HCC cells were examined.

resultsThe authors found that the expression of CLEC14A was markedly increased in hepatocellular carcinoma tumors in comparison with the adjacent tissue, and the expression level of CLEC14A was positively correlated with the size and differentiation of the tumor. Moreover, results of ROC analysis showed CLEC14A might function as a sensitive diagnostic biomarker for HCC. Furthermore, CLEC14A was up-regulated in HCC cell lines, and transient over-expression of CLEC14A decreased the proliferation and increased the apoptosis of HCC cells in vitro.

conclusionsOur results suggested that CLEC14A was up-regulated in HCC and might function as a potential diagnostic marker.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsApoptosisBiomarkersBiomarkers, TumorCell Adhesion MoleculesGene Expression Regulation, NeoplasticHumansLectins, C-TypeROC CurveBiomarkersBiomarkers, TumorCell Adhesion MoleculesCLEC14A protein, humanLectins, C-TypeCLEC14ADiagnosisHepatocellular carcinomaROC

Identifiers

PMID35576868
PMCPMC9118534
OpenAlexW4285193251

What OpenQuestion holds

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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.