Evidence map›Paper›PMID 29922854›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2018

fMLP-dependent activation of Akt and ERK1/2 through ROS/Rho A pathways is mediated through restricted activation of the FPRL1 (FPR2) receptor.

Wissam H Faour, Hussein Fayyad-Kazan, Nabil El Zein

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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. VIP modulates human macrophages phenotype via FPRL1 via activation of RhoA-GTPase and PLC pathways.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2021
    Article
  9. Review
  10. Review
  11. Aberrant DNA methylation levels of theAmerican journal of translational research · 2020
    Article
  12. The Role of Rho GTPases in Motility and Invasion of Glioblastoma Cells.Analytical cellular pathology (Amsterdam) · 2020
    Review
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

3 authors at 2 institutions in 1 country.

Wissam H FaourSchool of Medicine, Lebanese American University, P.O. Box 36, Byblos, Lebanon.
Hussein Fayyad-KazanFaculty of Sciences, Branch 1, Lebanese University, Rafic Hariri University Campus, Hadath, Lebanon.
Nabil El ZeinFaculty of Sciences, Branch 1, Lebanese University, Rafic Hariri University Campus, Hadath, Lebanon. nabilzein@hotmail.fr.
Lebanese University · LBLebanese American University · LB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

OBJECTIVE AND

designThe objective of this study is to uncover the signal transduction pathways of N-formyl methionyl-leucyl-phenylalanine (fMLP) in monocyte. MATERIALS OR SUBJECTS: Freshly isolated human peripheral blood monocytes (PBMC) were used for in vitro assessment of signal transduction pathways activated by fMLP. TREATMENT: Time-course and dose-response experiments were used to evaluate the effect of fMLP along with the specific inhibitors/stimulators on the activation of downstream signaling kinases.

methodsFreshly isolated human PBMC were stimulated with fMLP for the desired time. Western blot and siRNA analysis were used to evaluate the activated intracellular signaling kinases, and flow analysis was performed to assess the levels of CD11b. Furthermore, luminescence spectrometry was performed to measure the levels of released hydrogen peroxide in the media.

resultsfMLP strongly stimulated the activation of AKT and ERK1/2 through a RhoA-GTPase-dependent manner and also induced H

conclusionCollectively, these data suggested that fMLP-activated ERK1/2 and Akt pathways through specific activation of the FPRL1/ROS/RoA-GTPase pathway.

Indexed as

AnimalsCells, CulturedHumansHydrogen PeroxideLeukocytes, MononuclearMAP Kinase Signaling SystemN-Formylmethionine Leucyl-PhenylalanineProto-Oncogene Proteins c-aktRatsReceptors, Formyl PeptideReceptors, LipoxinrhoA GTP-Binding ProteinFPR2 protein, humanHydrogen PeroxideN-Formylmethionine Leucyl-PhenylalanineProto-Oncogene Proteins c-aktReceptors, Formyl PeptideReceptors, LipoxinrhoA GTP-Binding ProteinRHOA protein, humanFMLPFPRL1MonocytesRhoA-GTPase

Identifiers

PMID29922854
OpenAlexW2809647622

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.