Evidence map›Paper›PMID 36874381›Full record

ArticleHemaSphere2023

The CKS1/CKS2 Proteostasis Axis Is Crucial to Maintain Hematopoietic Stem Cell Function.

William Grey, Samantha Atkinson, Beatrice Rix, Pedro Casado, Linda Ariza-McNaughton, Cathy Hawley, Miriam L Sopoena, Katherine S Bridge, David Kent, Pedro R Cutillas and 1 more

Open access · goldAbstract read
In one paragraph

Article in HemaSphere, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.9field-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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
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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

11 authors at 3 institutions in 1 country.

William GreyYork Biomedical Research Institute, Department of Biology, University of York, United Kingdom.
Samantha AtkinsonHematopoietic Stem Cell Laboratory, The Francis Crick Institute, London, United Kingdom.
Beatrice RixYork Biomedical Research Institute, Department of Biology, University of York, United Kingdom.
Pedro CasadoCell Signalling and Proteomics Group, Centre for Genomics and Computational Biology, Bart's Cancer Institute, London, United Kingdom.
Linda Ariza-McNaughtonHematopoietic Stem Cell Laboratory, The Francis Crick Institute, London, United Kingdom.
Cathy HawleyYork Biomedical Research Institute, Department of Biology, University of York, United Kingdom.
Miriam L SopoenaBioinformatics Core, The Francis Crick Institute, London, United Kingdom.
Katherine S BridgeYork Biomedical Research Institute, Department of Biology, University of York, United Kingdom.
David KentYork Biomedical Research Institute, Department of Biology, University of York, United Kingdom.
Pedro R CutillasCell Signalling and Proteomics Group, Centre for Genomics and Computational Biology, Bart's Cancer Institute, London, United Kingdom.
Dominique BonnetHematopoietic Stem Cell Laboratory, The Francis Crick Institute, London, United Kingdom.
University of York · GBThe Francis Crick Institute · GBGenomics England · GB

Funding

Cancer Research UK FC001045Medical Research Council MR/X007146/1
6 · The paper itself

Abstract

Long-term hematopoietic stem cells are rare, highly quiescent stem cells of the hematopoietic system with life-long self-renewal potential and the ability to transplant and reconstitute the entire hematopoietic system of conditioned recipients. Most of our understanding of these rare cells has relied on cell surface identification, epigenetic, and transcriptomic analyses. Our knowledge of protein synthesis, folding, modification, and degradation-broadly termed protein homeostasis or "proteostasis"-in these cells is still in its infancy, with very little known about how the functional state of the proteome is maintained in hematopoietic stem cells. We investigated the requirement of the small phospho-binding adaptor proteins, the cyclin-dependent kinase subunits (CKS1 and CKS2), for maintaining ordered hematopoiesis and long-term hematopoietic stem cell reconstitution. CKS1 and CKS2 are best known for their roles in p27 degradation and cell cycle regulation, and by studying the transcriptome and proteome of

Identifiers

PMID36874381
PMCPMC9977483
OpenAlexW4322625392

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.