Evidence map›Paper›PMID 35014847›Full record

ArticleJournal of proteome research2022

SILAC Phosphoproteomics Reveals Unique Signaling Circuits in CAR-T Cells and the Inhibition of B Cell-Activating Phosphorylation in Target Cells.

Alijah A Griffith, Kenneth P Callahan, Nathan Gordo King, Qian Xiao, Xiaolei Su, Arthur R Salomon

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Single-Cell Proteomics: The Critical Role of Nanotechnology.International journal of molecular sciences · 2022
    Review
  13. 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

6 authors at 2 institutions in 1 country.

Alijah A GriffithDepartment of Molecular Biology, Cell Biology & Biochemistry, Brown University, Providence, Rhode Island 02912, United States.
Kenneth P CallahanDepartment of Molecular Biology, Cell Biology & Biochemistry, Brown University, Providence, Rhode Island 02912, United States.
Nathan Gordo KingDepartment of Molecular Biology, Cell Biology & Biochemistry, Brown University, Providence, Rhode Island 02912, United States.
Qian XiaoDepartment of Cell Biology, Yale School of Medicine, Yale University, New Haven, Connecticut 06520, United States.
Xiaolei SuDepartment of Cell Biology, Yale School of Medicine, Yale University, New Haven, Connecticut 06520, United States.
Arthur R SalomonDepartment of Molecular Biology, Cell Biology & Biochemistry, Brown University, Providence, Rhode Island 02912, United States.ORCID 0000-0002-7223-8996
Brown University · USYale University · US

Funding

Yale SPORE in Skin CancerP50CA121974 · NCI · YALE UNIVERSITY · PI MARCUS W BOSENBERG, Harriet M. Kluger · 2006 to 2026
$43.9M
Understand the metabolic fitness of naïve T cellsP01AI091580 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JEROEN ROOSE · 2011 to 2026
$31.1M
Translational Regulation in Normal Erythropoiesis and Diamond Blackfan AnemiaP20GM121293 · NIGMS · ARKANSAS CHILDREN'S HOSPITAL RES INST · PI Alan Tackett · 2017 to 2026
$27.6M
Supplement for Google cloud build-outR24GM137786 · NIGMS · UNIV OF ARKANSAS FOR MED SCIS · PI Alan Tackett · 2020 to 2026
$15.4M
Predoctoral Training in Molecular, Cellular, and Biochemical SciencesT32GM136566 · NIGMS · BROWN UNIVERSITY · PI Mark Aikens Johnson, Erica Nicole Larschan · 2020 to 2026
$3.1M
Spatial Organization of Membrane SignalingR35GM138299 · NIGMS · YALE UNIVERSITY · PI SU, XIAOLEI · 2020 to 2024
$2.3M
NCI NIH HHS P50 CA121974NIAID NIH HHS P01 AI091580NIGMS NIH HHS P20 GM121293NIGMS NIH HHS R24 GM137786NIGMS NIH HHS R35 GM138299NIGMS NIH HHS T32 GM136566
6 · The paper itself

Abstract

Chimeric antigen receptor (CAR) is a single-pass transmembrane receptor designed to specifically target and eliminate cancers. While CARs prove highly efficacious against B cell malignancies, the intracellular signaling events which promote CAR T cell activity remain elusive. To gain further insight into both CAR T cell signaling and the potential signaling response of cells targeted by CAR, we analyzed phosphopeptides captured by two separate phosphoenrichment strategies from third generation CD19-CAR T cells cocultured with SILAC labeled Raji B cells by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Here, we report that CD19-CAR T cells upregulated several key phosphorylation events also observed in canonical T cell receptor (TCR) signaling, while Raji B cells exhibited a significant decrease in B cell receptor-signaling related phosphorylation events in response to coculture. Our data suggest that CD19-CAR stimulation activates a mixture of unique CD19-CAR-specific signaling pathways and canonical TCR signaling, while global phosphorylation in Raji B cells is reduced after association with the CD19-CAR T cells.

Indexed as

Tandem Mass SpectrometryT-LymphocytesChromatography, LiquidPhosphorylationReceptors, Antigen, T-CellSignal TransductionReceptors, Antigen, T-Cellchimeric antigen receptorimmunotherapySILAC cell cocultureSrc SH2 superbinderT cell signalingtumor associated antigen

Identifiers

PMID35014847
PMCPMC8830406
OpenAlexW4221032946

What OpenQuestion holds

Textmetadata
LicenceTDM
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.