Evidence map›Paper›PMID 17118337›Full record

ArticleBiochemical and biophysical research communications2007

Peptide modulators of Src activity in G1 regulate entry into S phase and proliferation of NIH 3T3 cells.

Vidya Mamidipudi, Laura D Miller, Daria Mochly-Rosen, Christine A Cartwright

Open access · greenAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.1field-weighted citation impact, top 47% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Rack1 maintains intestinal homeostasis by protecting the integrity of the epithelial barrier.American journal of physiology. Gastrointestinal and liver physiology · 2018
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. RACK1, A multifaceted scaffolding protein: Structure and function.Cell communication and signaling : CCS · 2011
    Article
  7. Article
  8. Structure of a signal transduction regulator, RACK1, from Arabidopsis thaliana.Protein science : a publication of the Protein Society · 2008
    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

4 authors at 1 institution in 1 country.

Vidya MamidipudiDepartment of Medicine, Stanford University School of Medicine, Stanford, CA 94305-5187, USA.
Laura D Miller
Daria Mochly-Rosen
Christine A Cartwright
Stanford University · US

Funding

INTESTINAL CELL GROWTH CONTROL: ROLE OF TYROSINE KINASESR01DK043743 · NIDDK · STANFORD UNIVERSITY · PI CARTWRIGHT, CHRISTINE ANN · 1996 to 2015
$4.3M
INTESTINAL CELL GROWTH CONTROL--ROLE OF TYROSINE KINASER29DK043743 · NIDDK · STANFORD UNIVERSITY · PI CARTWRIGHT, CHRISTINE ANN · 1991 to 1995
–
NIDDK NIH HHS DK43743NIDDK NIH HHS DK65339NIDDK NIH HHS R01 DK043743
6 · The paper itself

Abstract

Cascades of kinases and phosphatases are regulated by selective protein-protein interactions that are essential for signal transduction. Peptide modulators of these interactions have been used to dissect the function of individual components of the signaling cascade, without relying on either the over- or underexpression of proteins. Previously, we identified RACK1 as an endogenous substrate, binding partner and inhibitor of Src tyrosine kinases. Here, we utilized cell-permeable peptides that selectively disrupt or enhance the interaction of RACK1 and Src to further examine the function of RACK1. Our results provide direct physiologic evidence that RACK1 regulates growth of NIH3T3 cells by suppressing the activity of Src and other cell cycle regulators in G1, and delaying entry into S phase. They also demonstrate the potential for using peptide modulators of Src activity as a tool for regulating cell growth, and for designing new strategies for cancer therapy that target specific protein-protein interactions.

Indexed as

AnimalsCell ProliferationG1 PhaseMiceNeuropeptidesNIH 3T3 CellsPeptidesProto-Oncogene Proteins pp60(c-src)Receptors for Activated C KinaseS PhaseNeuropeptidesPeptidesProto-Oncogene Proteins pp60(c-src)RACK1 protein, mouseReceptors for Activated C Kinase

Identifiers

PMID17118337
PMCPMC1850988
OpenAlexW2083138744

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.