Evidence map›Paper›PMID 28922551›Full record

ArticleJournal of cellular and molecular medicine2018

Lectin BS-I inhibits cell migration and invasion via AKT/GSK-3β/β-catenin pathway in hepatocellular carcinoma.

Qiang Jian, Zhao Yang, Jian Shu, Xiawei Liu, Jing Zhang, Zheng Li

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

11 citing papers in PubMed, 13 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

6 authors at 1 institution in 1 country.

Qiang JianLaboratory for Functional Glycomics, College of Life Sciences, Northwest University, Xi'an, Shaanxi Province, China.
Zhao YangLaboratory for Functional Glycomics, College of Life Sciences, Northwest University, Xi'an, Shaanxi Province, China.
Jian ShuLaboratory for Functional Glycomics, College of Life Sciences, Northwest University, Xi'an, Shaanxi Province, China.
Xiawei LiuLaboratory for Functional Glycomics, College of Life Sciences, Northwest University, Xi'an, Shaanxi Province, China.
Jing ZhangLaboratory of Tissue Engineering, Faculty of Life Science, Northwest University, Xi'an, Shaanxi Province, China.
Zheng LiLaboratory for Functional Glycomics, College of Life Sciences, Northwest University, Xi'an, Shaanxi Province, China.ORCID 0000-0002-1839-3450
Northwest University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is most common malignant cancer worldwide; however, the mortality rate of HCC remains high due to the invasion and metastasis of HCC. Thus, exploring novel treatments to prevent the invasion of HCC is needed for improving clinical outcome of this fatal disease. In this study, we identified lectin from Bandeiraea simplicifolia seeds (BS-I) binds to metastasis-associated HCC cell surface glycans by a lectin microarray and inhibits HCC cell migration and invasion through downregulating the matrix metalloproteinase 2 (MMP2), matrix metalloproteinase 9 (MMP9) and urokinase-type plasminogen activator (uPA) production. These effects of BS-I were mediated by inhibiting the activation of AKT/GSK-3β/β-catenin pathway and depended on specificity of lectin BS-I binding to GalNAc. GSK3β inhibitors rescued BS-I-mediated inhibition of migration and invasion of HCC cell. Further, we identified that lectin BS-I interacts with sGrp78, affects membrane localization of sGrp78 and attenuates the binding of sGrp78 and p85 to inhibit the activation of AKT/GSK-3β/β-catenin pathway. Overexpression of Grp78 or P85 rescues BS-I-mediated inhibition of migration and invasion of HCC cell. These findings demonstrated for the first time that BS-I can act as a novel potential drug to prevent the invasion of HCC.

Indexed as

Acetylgalactosaminebeta CateninCarcinoma, HepatocellularCell Line, TumorCell MovementEndoplasmic Reticulum Chaperone BiPGlycogen Synthase Kinase 3 betaHeat-Shock ProteinsHumansLectinsLiver NeoplasmsMembrane GlycoproteinsNeoplasm InvasivenessNeoplasm MetastasisProto-Oncogene Proteins c-aktSignal TransductionAcetylgalactosaminebeta CateninEndoplasmic Reticulum Chaperone BiPGlycogen Synthase Kinase 3 betaHeat-Shock ProteinsHSPA5 protein, humanLectinsMembrane GlycoproteinsProto-Oncogene Proteins c-aktAKT/GSK-3β/β-catenin pathwayGlycosylationGRP78hepatocellular carcinomalectin microarray

Identifiers

PMID28922551
PMCPMC5742741
OpenAlexW2755042304

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.