Evidence map›Paper›PMID 28205613›Full record

ArticleScientific reports2017

PAK4 interacts with p85 alpha: implications for pancreatic cancer cell migration.

Helen King, Kiruthikah Thillai, Andrew Whale, Prabhu Arumugam, Hesham Eldaly, Hemant M Kocher, Claire M Wells

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 42 citations in OpenAlex.

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  8. The Role of PIK3R1 in Metabolic Function and Insulin Sensitivity.International journal of molecular sciences · 2023
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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

7 authors at 3 institutions in 1 country.

Helen KingDivision of Cancer Studies, King's College London, UK.
Kiruthikah ThillaiDivision of Cancer Studies, King's College London, UK.
Andrew WhaleDivision of Cancer Studies, King's College London, UK.
Prabhu ArumugamBarts Cancer Institute, a CRUK centre of Excellance, Queen Mary University of London, UK.
Hesham EldalyDept of Haematopathology Oncology Diagnostic Service, Addenbrooke's Hospital, Cambridge, UK.
Hemant M KocherBarts Cancer Institute, a CRUK centre of Excellance, Queen Mary University of London, UK.
Claire M WellsDivision of Cancer Studies, King's College London, UK.
King's College London · GBQueen Mary University of London · GBAddenbrooke's Hospital · GB

Funding

Cancer Research UK C51714/A18521Cancer Research UK C7125/A3847Wellcome Trust 104485/Z/14/Z
6 · The paper itself

Abstract

It has been reported that p21-activated kinase 4 (PAK4) is amplified in pancreatic cancer tissue. PAK4 is a member of the PAK family of serine/threonine kinases, which act as effectors for several small GTPases, and has been specifically identified to function downstream of HGF-mediated c-Met activation in a PI3K dependent manner. However, the functionality of PAK4 in pancreatic cancer and the contribution made by HGF signalling to pancreatic cancer cell motility remain to be elucidated. We now find that elevated PAK4 expression is coincident with increased expression levels of c-Met and the p85α subunit of PI3K. Furthermore, we demonstrate that pancreatic cancer cells have a specific motility response to HGF both in 2D and 3D physiomimetic organotypic assays; which can be suppressed by inhibition of PI3K. Significantly, we report a specific interaction between PAK4 and p85α and find that PAK4 deficient cells exhibit a reduction in Akt phosphorylation downstream of HGF signalling. These results implicate a novel role for PAK4 within the PI3K pathway via interaction with p85α. Thus, PAK4 could be an essential player in PDAC progression representing an interesting therapeutic opportunity.

Indexed as

Cell Line, TumorCell MovementClass Ia Phosphatidylinositol 3-KinaseGene Expression Regulation, NeoplasticHepatocyte Growth FactorHumansMultigene Familyp21-Activated KinasesPancreatic NeoplasmsPhosphorylationProtein BindingProtein Interaction Domains and MotifsProto-Oncogene Proteins c-aktras ProteinsSignal TransductionClass Ia Phosphatidylinositol 3-KinaseHepatocyte Growth FactorHGF protein, humanp21-Activated KinasesPAK4 protein, humanProto-Oncogene Proteins c-aktras Proteins

Identifiers

PMID28205613
PMCPMC5312077
OpenAlexW2588869397

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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.