Evidence map›Paper›PMID 30677226›Full record

ArticleJournal of cellular and molecular medicine2019

Knockdown of Golgi phosphoprotein 73 blocks the trafficking of matrix metalloproteinase-2 in hepatocellular carcinoma cells and inhibits cell invasion.

Yiming Liu, Xiaodi Zhang, Sining Zhou, Jieyao Shi, Yun Xu, Jia He, Feng Lin, Anbang Wei, Linfu Zhou, Zhi Chen

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 24% 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

22 citing papers in PubMed, 27 citations in OpenAlex.

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  16. Assessment of liver cancer biomarkers.Gastroenterology and hepatology from bed to bench · 2020
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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

10 authors at 2 institutions in 1 country.

Yiming LiuState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Disease, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xiaodi ZhangState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Disease, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Sining ZhouDepartment of Biochemistry and Molecular Biology, Zhejiang University School of Medicine, Hangzhou, China.
Jieyao ShiDepartment of Biochemistry and Molecular Biology, Zhejiang University School of Medicine, Hangzhou, China.
Yun XuDepartment of Pathology and Pathophysiology Program in Molecular Cell Biology, Zhejiang University School of Medicine, Hangzhou, China.
Jia HeInstitute of Immunology, Zhejiang University School of Medicine, Hangzhou, China.
Feng LinInstitute of Immunology, Zhejiang University School of Medicine, Hangzhou, China.
Anbang WeiState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Disease, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Linfu ZhouDepartment of Biochemistry and Molecular Biology, Zhejiang University School of Medicine, Hangzhou, China.
Zhi ChenState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Disease, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Zhejiang University · CNFirst Affiliated Hospital Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Golgi phosphoprotein 73 (GP73) has been regarded as a novel serum biomarker for the diagnosis of hepatocellular carcinoma (HCC) in recent years. It has been reported that the upregulation of GP73 may promote the carcinogenesis and metastasis of HCC; however, the mechanisms remain poorly understood. In this study, GP73 correlates positively with matrix metalloproteinase-2 (MMP-2) in HCC-related cells and tissues. Further studies indicate that the knockdown of GP73 blocks MMP-2 trafficking and secretion, resulting in cell invasion inhibition. Additionally, the knockdown of GP73 induces the accumulation of intracellular MMP-2, which inhibits the phosphorylation of Src at Y416 and triggers the inhibition of SAPK/JNK and p53-p21 signalling pathways through a negative feedback loop. Finally, the transactivation of MMP2 was inhibited by the reduction in E2F1. This study reveals that GP73 plays functional roles in the trafficking and equilibrium of epithelial-mesenchymal transition (EMT)-related secretory proteins and that GP73 serves as a new potential target for combating the metastasis of HCC.

Indexed as

Carcinoma, HepatocellularCell Line, TumorE2F1 Transcription FactorEpithelial-Mesenchymal TransitionFeedback, PhysiologicalFemaleGene Expression Regulation, NeoplasticHumansLiver NeoplasmsMaleMatrix Metalloproteinase 2Membrane ProteinsNeoplasm InvasivenessPhosphorylationProtein TransportE2F1 protein, humanE2F1 Transcription FactorGOLM1 protein, humanMatrix Metalloproteinase 2Membrane ProteinsGP73hepatocellular carcinomaintrahepatic metastasisMMP-2negative feedback loopprotein trafficking

Identifiers

PMID30677226
PMCPMC6433683
OpenAlexW2914406967

What OpenQuestion holds

Textmetadata
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.