Evidence map›Paper›PMID 26722507›Full record

ArticleInternational journal of clinical and experimental pathology2015

The role of C/EBP-α expression in human liver and liver fibrosis and its relationship with autophagy.

Li-Li Tao, Yin-Zhen Zhai, Di Ding, Wei-Hua Yin, Xiu-Ping Liu, Guang-Yin Yu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

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  10. [Role of PPAR-γ-regulated autophagy in genistein-induced inhibition of hepatic stellate cell activation].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2019
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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

6 authors at 1 institution in 1 country.

Li-Li TaoDepartment of Pathology, Peking University, Shenzhen Hospital China.
Yin-Zhen ZhaiDepartment of Pathology, School of Basic Medical Sciences, Fudan University Shanghai 200032, China.
Di DingDepartment of Pathology, Fudan University Affliated Zhongshan Hospital Shanghai 200032, China.
Wei-Hua YinDepartment of Pathology, Peking University, Shenzhen Hospital China.
Xiu-Ping LiuDepartment of Pathology, School of Basic Medical Sciences, Fudan University Shanghai 200032, China.
Guang-Yin YuDepartment of Pathology, Peking University, Shenzhen Hospital China.
Shanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate the expression of CCAAT enhancer binding protein-α (C/EBP-α) in normal human liver and liver fibrosis and its probable association with autophagy.

methodsDouble label immunohistochemistry was used to detect the location of C/EBP-α in hepatocytes and hepatic stellate cells (HSCs). The expression of C/EBP-α, Atg5, and Atg6 was also evaluated by immunohistochemistry in paraffin sections of human liver. HSC-T6 cells were treated with rapamycin and 3-methyladenine (3MA) to induce or inhibit autophagy, and the expression of C/EBP-α protein was detected by Western blotting.

resultsDouble label immunohistochemistry showed that C/EBP-α was predominantly located in hepatocytes and that its expression was significantly decreased in fibrosis compared with normal liver. Atg5 expression was increased in fibrosis but was located primarily in liver septa and peri-vascular areas, which was consistent with the distribution of HSCs. In contrast, Atg6 was not expressed in normal or fibrotic liver. Treatment of HSC-T6 cells in culture with rapamycin or 3MA decreased or increased C/EBP-α expression, respectively, as shown by Western blotting.

conclusionC/EBP-α was primarily expressed in hepatocytes in normal liver, but its expression decreased significantly in liver fibrosis. Autophagy might play a role in liver fibrosis through its association with C/EBP-α, but this hypothesis warrants further investigation.

Indexed as

AutophagyBlotting, WesternCCAAT-Enhancer-Binding Protein-alphaHepatic Stellate CellsHepatocytesHumansImmunohistochemistryLiverLiver CirrhosisCCAAT-Enhancer-Binding Protein-alphaautophagyC/EBP-αhepatic stellate cellshepatocytes

Identifiers

PMID26722507
PMCPMC4680452
OpenAlexW2417480590

What OpenQuestion holds

Textmetadata
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.