Evidence map›Paper›PMID 29188802›Full record

ArticleActa pharmacologica Sinica2018

The LPI/GPR55 axis enhances human breast cancer cell migration via HBXIP and p-MLC signaling.

Xiao-Lei Zhou, Xin Guo, Yu-Pin Song, Chong-Yue Zhu, Wei Zou

Open access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

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  19. A Guide to Targeting the Endocannabinoid System in Drug Design.International journal of molecular sciences · 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

5 authors at 3 institutions in 2 countries.

Xiao-Lei ZhouPublic R&D Center of Bio-Manufacture, Hebei University of Science and Technology, Shijiazhuang 050018, China.
Xin GuoDepartment of Molecular and Cellular Pathology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8544, Japan.
Yu-Pin SongCollege of Chemical Engineering, Shijiazhuang University, Shijiazhuang 050035, China.
Chong-Yue ZhuPublic R&D Center of Bio-Manufacture, Hebei University of Science and Technology, Shijiazhuang 050018, China.
Wei ZouPublic R&D Center of Bio-Manufacture, Hebei University of Science and Technology, Shijiazhuang 050018, China.
Hebei University of Science and Technology · CNKagoshima University · JPShijiazhuang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The G protein-coupled receptor 55 (GPR55) is expressed in multiple tissues, and has been implicated in cancer pathogenesis, but little is known about its role in the migratory behavior of cancer cells, particularly breast cancer cells. In this study we first showed that GPR55 expression levels in 38 metastatic lymph nodes of breast cancer patients were profoundly elevated, and were positively associated in human breast cancer cells with their migratory ability. Moreover, the plasma levels of GPR55 endogenous agonist L-a-lysophosphatidylinositol (LPI) were significantly increased in breast cancer patients compared with healthy individuals. In human breast cancer LM-MCF-7 and MDA-MB-231 cells, treatment with LPI (2.5 μmol/L) significantly increased filopodia formation and resulted in cell migration, which could be blocked either by the GPR55 antagonist CID16020046 or by siRNA-mediated GPR55 knockdown. Furthermore, dual-luciferase report gene assays showed that GPR55 upregulated HBXIP at the promoter; GPR55 expression levels were positively correlated with HBXIP expression levels in breast cancer tissues and 8 breast cancer cell lines. We also showed that the LPI/GPR55 axis promoted the migration of breast cancer cells via two mutually exclusive pathways - the HBXIP/p-ERK1/2/Capn4 and MLCK/MLC signaling pathways. In xenograft nude mouse model, loss of GPR55 mainly affected breast cancer cell metastasis and the formation of metastatic foci. Thus, GPR55 is involved in the migratory behavior of human breast cancer cells and could serve as a pharmacological target for preventing metastasis.

Indexed as

Signal TransductionAdaptor Proteins, Signal TransducingAnimalsAzabicyclo CompoundsBenzoatesBreast NeoplasmsCell Line, TumorCell MovementFemaleHumansLysophospholipidsMiceReceptors, CannabinoidReceptors, G-Protein-CoupledRNA, Small InterferingUp-Regulation4-(4-(3-hydroxyphenyl)-3-(4-methylphenyl)-6-oxo-1H,4H,5H,6H-pyrrolo(3,4-c)pyrazol-5-yl)benzoic acidAdaptor Proteins, Signal TransducingAzabicyclo CompoundsBenzoatesGPR55 protein, humanLAMTOR5 protein, humanlysophosphatidylinositolLysophospholipidsReceptors, CannabinoidReceptors, G-Protein-CoupledRNA, Small Interfering

Identifiers

PMID29188802
PMCPMC5843836
OpenAlexW2773114504

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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.