Evidence map›Paper›PMID 24335650›Full record

ArticleNature cell biology2014

Stem cell quiescence acts as a tumour suppressor in squamous tumours.

A C White, J K Khuu, C Y Dang, J Hu, K V Tran, A Liu, S Gomez, Z Zhang, R Yi, P Scumpia and 2 more

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
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  3. How much do we know about the metastatic process?Clinical & experimental metastasis · 2024
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  5. The journey from melanocytes to melanoma.Nature reviews. Cancer · 2023
    Review
  6. Review
  7. MicroRNA-205 promotes hair regeneration by modulating mechanical properties of hair follicle stem cells.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Effects of UV Induced-Photoaging on the Hair Follicle Cycle of C57BL6/J Mice.Clinical, cosmetic and investigational dermatology · 2021
    Article
  16. Review
  17. Article
  18. OncogenicLife science alliance · 2020
    Article
  19. Review
  20. Review
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

12 authors at 3 institutions in 1 country.

A C White1] Department of Molecular Cell and Developmental Biology, UCLA, California 90095, USA [2] Eli and Edythe Broad Center for Regenerative Medicine, UCLA, California 90095, USA.
J K Khuu1] Department of Molecular Cell and Developmental Biology, UCLA, California 90095, USA [2] Eli and Edythe Broad Center for Regenerative Medicine, UCLA, California 90095, USA.
C Y Dang1] Department of Molecular Cell and Developmental Biology, UCLA, California 90095, USA [2] Eli and Edythe Broad Center for Regenerative Medicine, UCLA, California 90095, USA.
J Hu1] Department of Molecular Cell and Developmental Biology, UCLA, California 90095, USA [2] Eli and Edythe Broad Center for Regenerative Medicine, UCLA, California 90095, USA.
K V Tran1] Department of Molecular Cell and Developmental Biology, UCLA, California 90095, USA [2] Eli and Edythe Broad Center for Regenerative Medicine, UCLA, California 90095, USA.
A Liu1] Department of Molecular Cell and Developmental Biology, UCLA, California 90095, USA [2] Eli and Edythe Broad Center for Regenerative Medicine, UCLA, California 90095, USA.
S Gomez1] Department of Molecular Cell and Developmental Biology, UCLA, California 90095, USA [2] Eli and Edythe Broad Center for Regenerative Medicine, UCLA, California 90095, USA.
Z ZhangDepartment of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, Colorado 80309, USA.
R YiDepartment of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder, Colorado 80309, USA.
P ScumpiaDepartment of Medicine, Division of Dermatology, David Geffen School of Medicine, UCLA, California 90095, USA.
M Grigorian1] Department of Molecular Cell and Developmental Biology, UCLA, California 90095, USA [2] Eli and Edythe Broad Center for Regenerative Medicine, UCLA, California 90095, USA.
W E Lowry1] Department of Molecular Cell and Developmental Biology, UCLA, California 90095, USA [2] Eli and Edythe Broad Center for Regenerative Medicine, UCLA, California 90095, USA [3] Jonsson Cancer Research Center, UCLA, California 90095, USA [4] Molecular Biology Institute, UCLA, California 90095, USA.
Broad Center · USUniversity of Colorado Boulder · USUniversity of California, Los Angeles · US

Funding

TUMOR CELL SURFACES AND CHROMOSOMEST32CA009056 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Gay M Crooks, David A. Nathanson · 1985 to 2026
$10.5M
MicroRNA-mediated Regulation in Mammalian SkinR01AR059697 · NIAMS · UNIVERSITY OF COLORADO · PI YI, RUI · 2010 to 2020
$3.9M
Identification and characterization of cancer cells of origin in the epidermisR01AR057409 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LOWRY, WILLIAM E · 2010 to 2014
$1.7M
NCI NIH HHS T32 CA009056NIAMS NIH HHS 5R01AR057409-03NIAMS NIH HHS R01 AR057409NIAMS NIH HHS R01 AR059697
6 · The paper itself

Abstract

In some organs, adult stem cells are uniquely poised to serve as cancer cells of origin. It is unclear, however, whether tumorigenesis is influenced by the activation state of the adult stem cell. Hair follicle stem cells (HFSCs) act as cancer cells of origin for cutaneous squamous cell carcinoma and undergo defined cycles of quiescence and activation. The data presented here show that HFSCs are unable to initiate tumours during the quiescent phase of the hair cycle, indicating that the mechanisms that keep HFSCs dormant are dominant over the gain of oncogenes (such as Ras) or the loss of tumour suppressors (such as p53). Furthermore, Pten activity is necessary for quiescence-based tumour suppression, as its deletion alleviates tumour suppression without affecting proliferation. These data demonstrate that stem cell quiescence is a form of tumour suppression in HFSCs, and that Pten plays a role in maintaining quiescence in the presence of tumorigenic stimuli.

Indexed as

Cell CycleAdultAnimalsCarcinoma, Squamous CellCell ProliferationDisease ProgressionFlow CytometryGene DeletionGene Expression ProfilingGene Expression Regulation, NeoplasticHair FollicleHumansHyperplasiaIntegrasesMiceMutant ProteinsCre recombinaseHras protein, mouseIntegrasesKRAS protein, humanMutant ProteinsProto-Oncogene ProteinsProto-Oncogene Proteins p21(ras)PTEN Phosphohydrolaseras ProteinsTranscription FactorsTumor Suppressor Protein p53

Identifiers

PMID24335650
PMCPMC3874399
OpenAlexW1964818845

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.