Evidence map›Paper›PMID 20660630›Full record

ArticleThe Journal of cell biology2010

Ras-mediated activation of the TORC2-PKB pathway is critical for chemotaxis.

Huaqing Cai, Satarupa Das, Yoichiro Kamimura, Yu Long, Carole A Parent, Peter N Devreotes

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

90 citing papers in PubMed, 132 citations in OpenAlex.

  1. Article
  2. Article
  3. Loss of Copine D Leads to Ras Activation inbioRxiv : the preprint server for biology · 2026
    Article
  4. Signaling and actin waves at a glance.Journal of cell science · 2025
    Review
  5. Article
  6. Two endogenousProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
  8. Article
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  15. Article
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  17. Article
  18. Article
  19. Gradients of PI(4,5)PFrontiers in cell and developmental biology · 2022
    Article
  20. Article

30 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 1 country.

Huaqing CaiDepartment of Cell Biology, Johns Hopkins University, School of Medicine, Baltimore, MD 21205, USA.
Satarupa Das
Yoichiro Kamimura
Yu Long
Carole A Parent
Peter N Devreotes
Johns Hopkins Medicine · USCenter for Cancer Research · USJohns Hopkins University · USNational Institutes of Health · US

Funding

Temporal and Spatial Signaling in ChemotaxisR01GM034933 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI DEVREOTES, PETER N · 1987 to 2015
$8.8M
Signaling Networks in Chemotaxis and CytokinesisR37GM028007 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI DEVREOTES, PETER N · 2005 to 2014
$6.3M
Signaling Events Regulating ChemotaxisZIABC010418 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PARENT, CAROLE · 2009 to 2017
$4.6M
SIGNAL TRANSDUCTION AND DICTYOSTELIUM DEVELOPMENTR01GM028007 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI DEVREOTES, PETER N · 1985 to 2004
$2.4M
Intramural NIH HHSNIGMS NIH HHS GM 28007NIGMS NIH HHS GM 34933NIGMS NIH HHS R01 GM028007NIGMS NIH HHS R01 GM034933NIGMS NIH HHS R37 GM028007
6 · The paper itself

Abstract

In chemotactic cells, G protein-coupled receptors activate Ras proteins, but it is unclear how Ras-associated pathways link extracellular signaling to cell migration. We show that, in Dictyostelium discoideum, activated forms of RasC prolong the time course of TORC2 (target of rapamycin [Tor] complex 2)-mediated activation of a myristoylated protein kinase B (PKB; PKBR1) and the phosphorylation of PKB substrates, independently of phosphatidylinositol-(3,4,5)-trisphosphate. Paralleling these changes, the kinetics of chemoattractant-induced adenylyl cyclase activation and actin polymerization are extended, pseudopodial activity is increased and mislocalized, and chemotaxis is impaired. The effects of activated RasC are suppressed by deletion of the TORC2 subunit PiaA. In vitro RasC(Q62L)-dependent PKB phosphorylation can be rapidly initiated by the addition of a PiaA-associated immunocomplex to membranes of TORC2-deficient cells and blocked by TOR-specific inhibitor PP242. Furthermore, TORC2 binds specifically to the activated form of RasC. These results demonstrate that RasC is an upstream regulator of TORC2 and that the TORC2-PKB signaling mediates effects of activated Ras proteins on the cytoskeleton and cell migration.

Indexed as

AnimalsChemotaxisDictyosteliumEnzyme ActivationPhosphatidylinositol 3-KinasesPhosphorylationProtein Serine-Threonine KinasesProto-Oncogene Proteins c-aktProtozoan Proteinsras ProteinsRecombinant Fusion ProteinsSignal TransductionTranscription FactorsPhosphatidylinositol 3-KinasesPiaA protein, DictyosteliumPKBR-1 protein, DictyosteliumProtein Serine-Threonine KinasesProto-Oncogene Proteins c-aktProtozoan Proteinsras ProteinsRecombinant Fusion ProteinsTranscription Factors

Identifiers

PMID20660630
PMCPMC2930282
OpenAlexW2015273863

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.