Evidence map›Paper›PMID 12138200›Full record

ArticleMolecular and cellular biology2002

Site-directed perturbation of protein kinase C- integrin interaction blocks carcinoma cell chemotaxis.

Maddy Parsons, Melanie D Keppler, Adam Kline, Anthea Messent, Martin J Humphries, Ruth Gilchrist, Ian R Hart, Corinne Quittau-Prevostel, William E Hughes, Peter J Parker and 1 more

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

41 citing papers in PubMed, 101 citations in OpenAlex.

  1. Review
  2. The complexities of PKCα signaling in cancer.Advances in biological regulation · 2021
    Review
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  11. Time-domain microfluidic fluorescence lifetime flow cytometry for high-throughput Förster resonance energy transfer screening.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2015
    Article
  12. Review
  13. Review
  14. Article
  15. Involvement of PKCα activation in TF/VIIa/PAR2-induced proliferation, migration, and survival of colon cancer cell SW620.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013
    Article
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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

11 authors at 4 institutions in 2 countries.

Maddy ParsonsRichard Dimbleby/Cancer Research UK Department of Cancer Research, GKT School of Medicine, St. Thomas' Hospital, London SE1 7EH, United Kingdom.
Melanie D Keppler
Adam Kline
Anthea Messent
Martin J Humphries
Ruth Gilchrist
Ian R Hart
Corinne Quittau-Prevostel
William E Hughes
Peter J Parker
Tony Ng
Cancer Research UK · GBSt Thomas' Hospital · GBWellcome Centre for Cell-Matrix Research · GBUniversity of Manchester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polarized cell movement is an essential requisite for cancer metastasis; thus, interference with the tumor cell motility machinery would significantly modify its metastatic behavior. Protein kinase C alpha (PKC alpha) has been implicated in the promotion of a migratory cell phenotype. We report that the phorbol ester-induced cell polarization and directional motility in breast carcinoma cells is determined by a 12-amino-acid motif (amino acids 313 to 325) within the PKC alpha V3 hinge domain. This motif is also required for a direct association between PKC alpha and beta 1 integrin. Efficient binding of beta 1 integrin to PKC alpha requires the presence of both NPXY motifs (Cyto-2 and Cyto-3) in the integrin distal cytoplasmic domains. A cell-permeant inhibitor based on the PKC-binding sequence of beta 1 integrin was shown to block both PKC alpha-driven and epidermal growth factor (EGF)-induced chemotaxis. When introduced as a minigene by retroviral transduction into human breast carcinoma cells, this inhibitor caused a striking reduction in chemotaxis towards an EGF gradient. Taken together, these findings identify a direct link between PKC alpha and beta 1 integrin that is critical for directed tumor cell migration. Importantly, our findings outline a new concept as to how carcinoma cell chemotaxis is enhanced and provide a conceptual basis for interfering with tumor cell dissemination.

Indexed as

Nuclear ProteinsTranscription FactorsAmino Acid MotifsAntennapedia Homeodomain ProteinApoptosisBinding SitesBreast NeoplasmsChemotaxisFemaleHomeodomain ProteinsHumansIn Situ Nick-End LabelingIntegrin beta1IsoenzymesMicroscopy, FluorescencePeptidesAntennapedia Homeodomain ProteinHomeodomain ProteinsIntegrin beta1IsoenzymesNuclear ProteinsPeptidesPRKCA protein, humanProtein Kinase CProtein Kinase C-alphaRecombinant Fusion ProteinsTranscription Factors

Identifiers

PMID12138200
PMCPMC133968
OpenAlexW2122404551

What OpenQuestion holds

Textmetadata
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.