Evidence map›Paper›PMID 37243593›Full record

ArticleCell reports2023

PhosY-secretome profiling combined with kinase-substrate interaction screening defines active c-Src-driven extracellular signaling.

Sarah J Backe, SarahBeth D Votra, Matthew P Stokes, Endre Sebestyén, Matteo Castelli, Luca Torielli, Giorgio Colombo, Mark R Woodford, Mehdi Mollapour, Dimitra Bourboulia

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2023. 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
3.6field-weighted citation impact, top 7% 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, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Analysis of Limited Proteolysis-Coupled Mass Spectrometry Data.Molecular & cellular proteomics : MCP · 2025
    Article
  4. Hsp90: Bringing it all together.Cell stress & chaperones · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. 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

10 authors at 4 institutions in 2 countries.

Sarah J BackeDepartment of Urology, SUNY Upstate Medical University, Syracuse, NY 13210, USA; Upstate Cancer Center, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
SarahBeth D VotraDepartment of Urology, SUNY Upstate Medical University, Syracuse, NY 13210, USA; Upstate Cancer Center, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
Matthew P StokesCell Signaling Technology, Inc., Danvers, MA 01923, USA.
Endre SebestyénThe Bioinformatics CRO, Inc., Orlando, FL, USA.
Matteo CastelliDipartimento di Chimica, Università di Pavia, 27100 Pavia, Italy.
Luca TorielliDipartimento di Chimica, Università di Pavia, 27100 Pavia, Italy.
Giorgio ColomboDipartimento di Chimica, Università di Pavia, 27100 Pavia, Italy.
Mark R WoodfordDepartment of Urology, SUNY Upstate Medical University, Syracuse, NY 13210, USA; Department of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, NY 13210, USA; Upstate Cancer Center, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
Mehdi MollapourDepartment of Urology, SUNY Upstate Medical University, Syracuse, NY 13210, USA; Department of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, NY 13210, USA; Upstate Cancer Center, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
Dimitra BourbouliaDepartment of Urology, SUNY Upstate Medical University, Syracuse, NY 13210, USA; Department of Biochemistry and Molecular Biology, SUNY Upstate Medical University, Syracuse, NY 13210, USA; Upstate Cancer Center, SUNY Upstate Medical University, Syracuse, NY 13210, USA. Electronic address: bourmpod@upstate.edu.
SUNY Upstate Medical University · USUniversity of Pavia · ITCell Signaling Technology (United States) · USOrlando Immunology Center · US

Funding

Regulation of the extracellular HSP90 chaperone machineryR01GM139932 · NIGMS · UPSTATE MEDICAL UNIVERSITY · PI BOURBOULIA, DIMITRA · 2021 to 2024
$1.3M
NIGMS NIH HHS R01 GM139932
6 · The paper itself

Abstract

c-Src tyrosine kinase is a renowned key intracellular signaling molecule and a potential target for cancer therapy. Secreted c-Src is a recent observation, but how it contributes to extracellular phosphorylation remains elusive. Using a series of domain deletion mutants, we show that the N-proximal region of c-Src is essential for its secretion. The tissue inhibitor of metalloproteinases 2 (TIMP2) is an extracellular substrate of c-Src. Limited proteolysis-coupled mass spectrometry and mutagenesis studies verify that the Src homology 3 (SH3) domain of c-Src and the P

Indexed as

Protein-Tyrosine KinasesSecretomeCell CommunicationPhosphorylationPhosphotransferasesSignal Transductionsrc-Family Kinasessrc Homology DomainsPhosphotransferasesProtein-Tyrosine Kinasessrc-Family Kinasesblocking antibodiesCP: CancerCP: Molecular biologyphosphoproteomicpost-translational modificationPxxP motifsecretomeSrc tyrosine kinaseTIMP2tissue inhibitors of metalloproteinasestumor growth inhibition

Identifiers

PMID37243593
PMCPMC10569185
OpenAlexW4378192091

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.