Evidence map›Paper›PMID 32727598›Full record

ArticleJournal of experimental & clinical cancer research : CR2020

CD147 promotes collective invasion through cathepsin B in hepatocellular carcinoma.

Shi-Jie Wang, Dong Chao, Wei Wei, Gang Nan, Jia-Yue Li, Fen-Ling Liu, Ling Li, Jian-Li Jiang, Hong-Yong Cui, Zhi-Nan Chen

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

34 citing papers in PubMed, 51 citations in OpenAlex.

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  13. Acta pharmacologica Sinica · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Shi-Jie WangNational Translational Science Center for Molecular Medicine, Department of Cell Biology, Fourth Military Medical University, Xi'an, 710032, P. R. China.
Dong ChaoDepartment of thoracic surgery, the 940th hospital of joint logistics support force of Chinese People's Liberation Army, Lanzhou, 730050, P. R. China.
Wei WeiNational Translational Science Center for Molecular Medicine, Department of Cell Biology, Fourth Military Medical University, Xi'an, 710032, P. R. China.
Gang NanNational Translational Science Center for Molecular Medicine, Department of Cell Biology, Fourth Military Medical University, Xi'an, 710032, P. R. China.
Jia-Yue LiNational Translational Science Center for Molecular Medicine, Department of Cell Biology, Fourth Military Medical University, Xi'an, 710032, P. R. China.
Fen-Ling LiuNational Translational Science Center for Molecular Medicine, Department of Cell Biology, Fourth Military Medical University, Xi'an, 710032, P. R. China.
Ling LiNational Translational Science Center for Molecular Medicine, Department of Cell Biology, Fourth Military Medical University, Xi'an, 710032, P. R. China.
Jian-Li JiangNational Translational Science Center for Molecular Medicine, Department of Cell Biology, Fourth Military Medical University, Xi'an, 710032, P. R. China. jiangjl@fmmu.edu.cn.
Hong-Yong CuiNational Translational Science Center for Molecular Medicine, Department of Cell Biology, Fourth Military Medical University, Xi'an, 710032, P. R. China. cui-hongyong@163.com.ORCID https://orcid.org/0000-0003-0051-2666
Zhi-Nan ChenNational Translational Science Center for Molecular Medicine, Department of Cell Biology, Fourth Military Medical University, Xi'an, 710032, P. R. China. znchen@fmmu.edu.cn.
Air Force Medical University · CNChinese People's Liberation Army · CN

Funding

China Postdoctoral Science Foundation 2019M653970National Key Research and Development Program of China 2018YFA0109000National Natural Science Foundation of China 31601127National Natural Science Foundation of China 81602521National Postdoctoral Program for Innovative Talents BX20180376National Science and Technology Major Project 2017ZX10203205-004-002
6 · The paper itself

Abstract

backgroundMounting evidence suggests that solid tumors display the features of collective invasion, however, the molecular mechanisms are far from clear. This study aims to verify the role and the underlying mechanisms of CD147 in collective invasion in hepatocellular carcinoma.

methodsImmunostaining was used to analyze human hepatocellular carcinoma specimens and three-dimensional cultures. Three-dimensional invasion model was established to mimic in vivo invasion. RNA-sequencing was used to identify downstream effectors.

resultsHuman hepatocellular carcinoma underwent collective invasion and CD147 was observed to be upregulated at the invasive front of tumor cell groups. CD147 was demonstrated to promote collective invasion using the modified three-dimensional invasion model, which recapitulated the main features of collective invasion. Through transcriptome analysis and enzyme activity assay, we found that CD147 enhanced cathepsin B expression and activity. Upregulated cathepsin B in hepatocellular carcinoma cells facilitated migration and invasion, which mediated CD147-induced invasive phenotype in hepatocellular carcinoma. In terms of mechanism, we found that CD147 promoted cathepsin B transcription by activating β-catenin signaling as a result of reduced GSK-3β expression. Furthermore, we found that elevated expression of CD147 as well as cathepsin B were correlated with poor prognosis in patients with hepatocellular carcinoma.

conclusionsCD147 promotes hepatocellular carcinoma cells collective invasion via upregulating cathepsin B expression and targeting CD147 would be valuable for the development of novel therapeutic modalities against invasion and metastasis of cancer.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisBasiginBiomarkers, TumorCarcinoma, HepatocellularCathepsin BCell ProliferationHumansLiver NeoplasmsMiceMice, Inbred BALB CMice, NudeNeoplasm InvasivenessPrognosisSurvival RateBasiginBiomarkers, TumorBSG protein, humanCathepsin BCTSB protein, humanCathepsin BCD147Collective invasionHepatocellular carcinoma

Identifiers

PMID32727598
PMCPMC7391525
OpenAlexW3045997262

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.