Evidence map›Paper›PMID 29700307›Full record

ArticleCell death & disease2018

ZBTB20 regulates EGFR expression and hepatocyte proliferation in mouse liver regeneration.

Hai Zhang, Jian-Hui Shi, Hui Jiang, Kejia Wang, Jun-Yu Lu, Xuchao Jiang, Xianhua Ma, Yu-Xia Chen, An-Jing Ren, Jianming Zheng and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-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

17 citing papers in PubMed, 28 citations in OpenAlex.

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  13. [Establishment of animal models of epidermal growth factor receptor inhibitor-related rashes].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 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

14 authors at 2 institutions in 2 countries.

Hai ZhangDepartment of Pathophysiology, Second Military Medical University, Shanghai, 200433, China.
Jian-Hui ShiDepartment of Pathophysiology, Second Military Medical University, Shanghai, 200433, China.
Hui JiangDepartment of Pathophysiology, Second Military Medical University, Shanghai, 200433, China.
Kejia WangDepartment of Pathophysiology, Second Military Medical University, Shanghai, 200433, China.
Jun-Yu LuDepartment of Pathophysiology, Second Military Medical University, Shanghai, 200433, China.
Xuchao JiangDepartment of Pathophysiology, Second Military Medical University, Shanghai, 200433, China.
Xianhua MaDepartment of Pathophysiology, Second Military Medical University, Shanghai, 200433, China.
Yu-Xia ChenDepartment of Pathophysiology, Second Military Medical University, Shanghai, 200433, China.
An-Jing RenDepartment of Pathophysiology, Second Military Medical University, Shanghai, 200433, China.
Jianming ZhengDepartment of Pathology, Changhai Hospital, Shanghai, 200433, China.
Zhifang XieDepartment of Pathophysiology, Second Military Medical University, Shanghai, 200433, China.
Shaodong GuoDepartment of Nutrition and Metabolism, Texas University of Agriculture and Mechanics, College Station, TX, 77843, USA.
Xiongfei XuDepartment of Pathophysiology, Second Military Medical University, Shanghai, 200433, China. xiongfeixu@126.com.
Weiping J ZhangDepartment of Pathophysiology, Second Military Medical University, Shanghai, 200433, China. wzhang@smmu.edu.cn.ORCID 0000-0003-4727-2380
Second Military Medical University · CNTexas College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver has a unique regenerative capacity, however, its regulatory mechanism is not fully defined. We have established the zinc-finger protein ZBTB20 as a key transcriptional repressor for alpha-fetoprotein (AFP) gene in liver. As a marker of hepatic differentiation, AFP expression is closely associated with hepatocyte proliferation. Unexpectedly, here we showed that ZBTB20 acts as a positive regulator of hepatic replication and is required for efficient liver regeneration. The mice specifically lacking ZBTB20 in hepatocytes exhibited a remarkable defect in liver regeneration after partial hepatectomy, which was characterized by impaired hepatocyte proliferation along with delayed cyclin D1 induction and diminished AKT activation. Furthermore, we found that epithelial growth factor receptor (EGFR) expression was dramatically reduced in the liver in the absence of ZBTB20, thereby substantially attenuating the activation of EGFR signaling pathway in regenerating liver. Adenovirus-mediated EGFR overexpression in ZBTB20-deficient hepatocytes could largely restore AKT activation in response to EGFR ligands in vitro, as well as hepatocyte replication in liver regeneration. Furthermore, ZBTB20 overexpression could significantly restore hepatic EGFR expression and cell proliferation after hepatectomy in ZBTB20-deficient liver. Taken together, our data point to ZBTB20 as a critical regulator of EGFR expression and hepatocyte proliferation in mouse liver regeneration, and may serve as a potential therapeutic target in clinical settings of liver regeneration.

Indexed as

Cell ProliferationGene Expression RegulationLiver RegenerationAnimalsErbB ReceptorsHepatocytesLiverMaleMiceMice, KnockoutSignal TransductionTranscription FactorsEGFR protein, mouseErbB ReceptorsTranscription FactorsZbtb20 protein, mouse

Identifiers

PMID29700307
PMCPMC5920068
OpenAlexW2800800032

What OpenQuestion holds

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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.