Evidence map›Paper›PMID 28831039›Full record

ArticleNature communications2017

Exit from quiescence displays a memory of cell growth and division.

Xia Wang, Kotaro Fujimaki, Geoffrey C Mitchell, Jungeun Sarah Kwon, Kimiko Della Croce, Chris Langsdorf, Hao Helen Zhang, Guang Yao

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.8field-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

31 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Quiescence Multiverse.Biomolecules · 2025
    Review
  3. Biomaterials science · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. The molecular architecture of cell cycle arrest.Molecular systems biology · 2022
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Measuring Endocytosis During Proliferative Cell Quiescence.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  16. Cellular quiescence in budding yeast.Yeast (Chichester, England) · 2021
    Review
  17. Septins in Stem Cells.Frontiers in cell and developmental biology · 2021
    Review
  18. Review
  19. Article
  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

8 authors at 4 institutions in 2 countries.

Xia WangDepartment of Molecular and Cellular Biology, University of Arizona, Tucson, AZ, 85721, USA.
Kotaro FujimakiDepartment of Molecular and Cellular Biology, University of Arizona, Tucson, AZ, 85721, USA.
Geoffrey C MitchellDepartment of Molecular and Cellular Biology, University of Arizona, Tucson, AZ, 85721, USA.
Jungeun Sarah KwonDepartment of Molecular and Cellular Biology, University of Arizona, Tucson, AZ, 85721, USA.
Kimiko Della CroceDepartment of Molecular and Cellular Biology, University of Arizona, Tucson, AZ, 85721, USA.
Chris LangsdorfMolecular Probes, Thermo Fisher Scientific, Eugene, OR, 97402, USA.
Hao Helen ZhangDepartment of Mathematics, University of Arizona, Tucson, AZ, 85721, USA.
Guang YaoDepartment of Molecular and Cellular Biology, University of Arizona, Tucson, AZ, 85721, USA. guangyao@email.arizona.edu.
University of Arizona · USHefei University of Technology · CNThermo Fisher Scientific (United States) · USWofford College · US

Funding

Integrative Cancer Scholars Training GrantT32CA009213 · NCI · UNIVERSITY OF ARIZONA · PI CAREW, JENNIFER S, CURIEL-LEWANDROWSKI, CLARA · 1985 to 2024
$8.6M
Computational and Mathematical Modeling of Biomedical SystemsT32GM084905 · NIGMS · UNIVERSITY OF ARIZONA · PI SECOMB, TIMOTHY W. · 2009 to 2018
$2.2M
NCI NIH HHS T32 CA009213NIGMS NIH HHS T32 GM084905
6 · The paper itself

Abstract

Reactivating quiescent cells to proliferate is critical to tissue repair and homoeostasis. Quiescence exit is highly noisy even for genetically identical cells under the same environmental conditions. Deregulation of quiescence exit is associated with many diseases, but cellular mechanisms underlying the noisy process of exiting quiescence are poorly understood. Here we show that the heterogeneity of quiescence exit reflects a memory of preceding cell growth at quiescence induction and immediate division history before quiescence entry, and that such a memory is reflected in cell size at a coarse scale. The deterministic memory effects of preceding cell cycle, coupled with the stochastic dynamics of an Rb-E2F bistable switch, jointly and quantitatively explain quiescence-exit heterogeneity. As such, quiescence can be defined as a distinct state outside of the cell cycle while displaying a sequential cell order reflecting preceding cell growth and division variations.The quiescence-exit process is noisy even in genetically identical cells under the same environmental conditions. Here the authors show that the heterogeneity of quiescence exit reflects a memory of preceding cell growth at quiescence induction and immediate division history prior to quiescence entry.

Indexed as

AlgorithmsModels, BiologicalAnimalsCell CycleCell DivisionCell LineCell ProliferationCell SizeCulture MediaCulture Media, Serum-FreeE2F Transcription FactorsRatsRetinoblastoma ProteinTime FactorsCulture MediaCulture Media, Serum-FreeE2F Transcription FactorsRetinoblastoma Protein

Identifiers

PMID28831039
PMCPMC5567331
OpenAlexW2749580584

What OpenQuestion 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 OpenQuestion graph.