Evidence map›Paper›PMID 24603166›Full record

ReviewNature reviews. Immunology2014

New roles for cyclin-dependent kinases in T cell biology: linking cell division and differentiation.

Andrew D Wells, Peter A Morawski

Registry-linked trialAbstract readReview
In one paragraph

Review in Nature reviews. Immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03220178 (PRECYCLE), which is not on this map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
–field-weighted citation impact
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.

NCT03220178 phase4terminatednot on this mapstarted 2017, after this paper: background citation

PRECYCLE: Multicenter, Randomized Phase IV Intergroup Trial to Evaluate the Impact of eHealth-based Patient Reported Outcome (PRO) Assessment on Quality of Life in Patients With Hormone Receptor Positive, HER2 Negative Locally Advanced or Metastatic Breast Cancer Treated With Palbociclib and an Aromatase Inhibitor- or Palbociclib and Fulvestrant

TypeinterventionalSponsorPalleos Healthcare GmbHRan2017 to 2021Enrolled532ConditionsBreast NeoplasmArmsPalbociclib, Fulvestrant, Anastrozole, Letrozole, Exemestane
3 · Its place in the literature

Who cites it

47 citing papers in PubMed.

  1. Presenting features and outcomes to standard systemic therapies in patients with MTAP-deleted advanced non-small cell lung cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Interferon Epsilon Loss Is Elusive 9p21 Link to Immune-Cold Tumors, Resistant to Immune Checkpoint Therapy, and Endogenous CXCL9/10 Induction.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2025
    Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Green tea EGCG inhibits naïve CD4Current research in food science · 2023
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors.

Andrew D WellsDepartment of Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, USA; and The Children's Hospital of Philadelphia Research Institute, Abramson Research Center, 3615 Civic Center Boulevard, Philadelphia, Pennsylvania 19104, USA.
Peter A MorawskiDepartment of Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, USA; and The Children's Hospital of Philadelphia Research Institute, Abramson Research Center, 3615 Civic Center Boulevard, Philadelphia, Pennsylvania 19104, USA.

Funding

Growth Factor Signaling, Cell Division and T cell AnergyR01AI054643 · NIAID · CHILDREN'S HOSP OF PHILADELPHIA · PI WELLS, ANDREW D · 2002 to 2020
$5.7M
Regulation of Foxp3 FunctionR01AI070807 · NIAID · CHILDREN'S HOSP OF PHILADELPHIA · PI WELLS, ANDREW D · 2008 to 2012
$2.0M
Cyclin-dependent kinases: Novel switches in anergy and targets for toleranceR56AI054643 · NIAID · CHILDREN'S HOSP OF PHILADELPHIA · PI WELLS, ANDREW D · 2014 to 2014
$293k
NIAID NIH HHS AI054643NIAID NIH HHS AI070807NIAID NIH HHS R01 AI054643NIAID NIH HHS R01 AI070807NIAID NIH HHS R56 AI054643
6 · The paper itself

Abstract

The proliferation of a few antigen-reactive lymphocytes into a large population of effector cells is a fundamental property of adaptive immunity. The cell division that fuels this process is driven by signals from antigen, co-stimulatory molecules and growth factor receptors, and is controlled by the cyclin-dependent kinase (CDK) cascade. In this Opinion article, we discuss how the CDK cascade provides one potential link between cell division and differentiation through the phosphorylation of immunologically relevant transcription factors, and how components of this pathway might ultimately participate in the decision between tolerance and immunity.

Indexed as

Adaptive ImmunityAnimalsCell Cycle CheckpointsCell DifferentiationCell DivisionCyclin-Dependent Kinase Inhibitor p27Cyclin-Dependent KinasesHumansImmune ToleranceImmunologic MemoryImmunotherapyModels, ImmunologicalSignal TransductionT-LymphocytesCyclin-Dependent Kinase Inhibitor p27Cyclin-Dependent Kinases

Identifiers

PMID24603166
PMCPMC10114933

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.