Evidence map›Paper›PMID 30136190›Full record

ArticleMolecular and cellular biochemistry2019

HGF promotes HTR-8/SVneo cell migration through activation of MAPK/PKA signaling leading to up-regulation of WNT ligands and integrins that target β-catenin.

Piyush Chaudhary, Sudha Saryu Malhotra, Gosipatala Sunil Babu, Ranbir Chander Sobti, Satish Kumar Gupta

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In one paragraph

Article in Molecular and cellular biochemistry, 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 32% 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, 15 citations in OpenAlex.

  1. Article
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  7. Review
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  9. Oxidative stress activated by Keap-1/Nrf2 signaling pathway in pathogenesis of preeclampsia.International journal of clinical and experimental pathology · 2020
    Article
  10. Article
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 2 institutions in 1 country.

Piyush ChaudharyReproductive Cell Biology Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi, 110 067, India.
Sudha Saryu MalhotraReproductive Cell Biology Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi, 110 067, India.
Gosipatala Sunil BabuDepartment of Biotechnology, Babasaheb Bhimrao Ambedkar University, Vidya Vihar, Lucknow, 226 025, India.
Ranbir Chander SobtiBabasaheb Bhimrao Ambedkar University, Vidya Vihar, Lucknow, 226 025, India.
Satish Kumar GuptaReproductive Cell Biology Laboratory, National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi, 110 067, India. skgupta@nii.ac.in.ORCID http://orcid.org/0000-0003-3717-0436
Babasaheb Bhimrao Ambedkar University · INNational Institute of Immunology · IN

Funding

Department of Biotechnology, Ministry of Science and Technology BT/PR12312/MED/30/1424/2014Department of Health Research GIA/28/2014Science and Engineering Research Board SB/S2/JCB-040/2015
6 · The paper itself

Abstract

Inadequate migration and invasion of the trophoblast cells during embryo implantation is one of the reasons for pregnancy-related complications such as intrauterine growth restriction and preeclampsia. In the present study, relevance of WNT ligands and integrins associated with hepatocyte growth factor (HGF)-mediated migration of HTR-8/SVneo trophoblastic cells has been investigated. Treatment of HTR-8/SVneo cells with HGF led to a dose-dependent increase in their migration. RT-PCR studies revealed a significant increase in the transcripts of WNT4, WNT11, ITGA2, and ITGAV, which was further confirmed at protein level by Western blotting. HGF treatment also led to increased expression of integrin α2β1 and αVβ5 in HTR-8/SVneo cells. Silencing of WNT4, WNT11, ITGA2, and ITGAV by siRNA led to a significant decrease in HGF-mediated migration of cells. Treatment of cells with HGF led to activation of mitogen-activated protein kinases (MAPK) and protein kinase A (PKA) signaling pathways. Inhibition of MAPK/PKA, by selective inhibitors, led to decrease in the expression of above WNT ligands and integrins. Silencing of WNT4/WNT11 led to concomitant decrease in the expression of ITGA2 and ITGAV and vice versa. HGF treatment also led to significant increase in β-catenin expression, a downstream target of both WNT ligands and integrins. Silencing of β-catenin led to decrease in HGF-mediated migration. β-catenin expression was also down-regulated in WNT4/WNT11/ITGA2/ITGAV silenced cells suggesting a possible cross-communication of WNT ligands and integrins via β-catenin. These studies have established the significance of WNT4/WNT11 as well as ITGA2/ITGAV during HGF-mediated migration of HTR-8/SVneo trophoblastic cells.

Indexed as

beta CateninCell LineCell MovementCyclic AMP-Dependent Protein KinasesExtracellular Signal-Regulated MAP KinasesHepatocyte Growth FactorHumansIntegrinsMAP Kinase Signaling SystemTrophoblastsWnt4 ProteinWnt Proteinsbeta CateninCyclic AMP-Dependent Protein KinasesExtracellular Signal-Regulated MAP KinasesHepatocyte Growth FactorHGF protein, humanIntegrinsWnt11 protein, humanWnt4 ProteinWNT4 protein, humanWnt ProteinsCell migrationHepatocyte growth factorIntegrinsTrophoblastWNT ligandsβ-catenin

Identifiers

PMID30136190
OpenAlexW2888166221

What OpenQuestion holds

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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.