Evidence map›Paper›PMID 31493275›Full record

ArticleClinical and experimental medicine2019

MAT2B mediates invasion and metastasis by regulating EGFR signaling pathway in hepatocellular carcinoma.

Lijun Wu, Ping Chen, Jun Ying, Qi Zhang, Fuchen Liu, Bin Lv, Zhihui Che, Wenli Zhang, Mengmeng Wu, Jun Zhang and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Clinical and experimental medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Lijun WuDepartment of Digestive Diseases of Huashan Hosptial, Fudan University, Shanghai, 200040, China.
Ping ChenInstitutes of Biomedical Sciences, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Jun YingFudan University Library, Shanghai, 200433, China.
Qi ZhangInstitutes of Biomedical Sciences, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Fuchen LiuThe Third Department of Hepatic Surgery of Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, 200438, China.
Bin LvDepartment of Digestive Diseases of Huashan Hosptial, Fudan University, Shanghai, 200040, China.
Zhihui CheDepartment of Digestive Diseases of Huashan Hosptial, Fudan University, Shanghai, 200040, China.
Wenli ZhangDepartment of Digestive Diseases of Huashan Hosptial, Fudan University, Shanghai, 200040, China.
Mengmeng WuDepartment of Digestive Diseases of Huashan Hosptial, Fudan University, Shanghai, 200040, China.
Jun ZhangDepartment of Digestive Diseases of Huashan Hosptial, Fudan University, Shanghai, 200040, China.
Dongqin YangDepartment of Digestive Diseases of Huashan Hosptial, Fudan University, Shanghai, 200040, China. kobesakura@fudan.edu.cn.ORCID http://orcid.org/0000-0003-0126-5898
Jie LiuDepartment of Digestive Diseases of Huashan Hosptial, Fudan University, Shanghai, 200040, China. jieliu@fudan.edu.cn.
Fudan University · CNShanghai Medical College of Fudan University · CNSecond Military Medical University · CN

Funding

National Natural Science Foundation of China 81401980Natural Science Foundation and Major Basic Research Program of Shanghai 16JC1420104the Development Fund for Shanghai Talents 201660
6 · The paper itself

Abstract

The poor prognosis of hepatocellular carcinoma (HCC) patients is mainly due to cancer metastasis. Methionine adenosyltransferase 2β (MAT2B) encodes a regulatory subunit (β) for methionine adenosyltransferase. Previous studies reveal that MAT2B provides a growth advantage for HCC, but its role in metastasis is unknown. This study showed that both in the xenograft zebra fish model and in the lung metastasis model in nude mice, the stable inhibition of MAT2B could suppress the metastasis of HCC cancer cells. Silencing of MAT2B in HCC cell lines could remarkably inhibit migration and invasion. By analysis of human phospho-kinase array membranes, we found several differentially expressed proteins, including phosphor-AKT, phospho-EGFR, phospho-Src family, phospho-FAK, phospho-STAT3 and phospho-ERK. We further confirmed the change of these EGFR pathway-related proteins was in accordance with MAT2B expression pattern through immunoblotting test. Finally, we found that MAT2B was overexpressed in HCC caner tissues and correlated with poor prognosis for HCC patients in clinical manifestation. Our study demonstrated that silencing of MAT2B could suppress liver cancer cell migration and invasion through the inhibition of EGFR signaling, which suggested that MAT2B might serve as a new prognostic marker and therapeutic target for HCC.

Indexed as

AnimalsCarcinoma, HepatocellularCell MovementCell ProliferationErbB ReceptorsFemaleGene Expression Regulation, NeoplasticHep G2 CellsHumansLiver NeoplasmsLung NeoplasmsMaleMethionine AdenosyltransferaseMiceNeoplasm InvasivenessNeoplasm TransplantationEGFR protein, humanErbB ReceptorsMAT2B protein, humanMethionine AdenosyltransferaseEGFRHepatocellular carcinomaInvasionMAT2BMigration

Identifiers

PMID31493275
OpenAlexW2971571621

What OpenQuestion holds

Textmetadata
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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.