Evidence map›Paper›PMID 29595474›Full record

ArticleeLife2018

Size uniformity of animal cells is actively maintained by a p38 MAPK-dependent regulation of G1-length.

Shixuan Liu, Miriam Bracha Ginzberg, Nish Patel, Marc Hild, Bosco Leung, Zhengda Li, Yen-Chi Chen, Nancy Chang, Yuan Wang, Ceryl Tan and 6 more

Abstract read
In one paragraph

Article in eLife, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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.

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

43 citing papers in PubMed.

  1. Review
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  3. Review
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  7. Review
  8. A GeneralizedbioRxiv : the preprint server for biology · 2024
    Article
  9. Review
  10. Article
  11. The role ofJournal of pharmaceutical analysis · 2023
    Review
  12. Article
  13. Article
  14. Cell growth and the cell cycle: New insights about persistent questions.BioEssays : news and reviews in molecular, cellular and developmental biology · 2022
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Scaling of biosynthesis and metabolism with cell size.Molecular biology of the cell · 2022
    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

16 authors.

Shixuan Liu *Cell Biology Program, The Hospital for Sick Children, Toronto, Canada.
Miriam Bracha Ginzberg *Cell Biology Program, The Hospital for Sick Children, Toronto, Canada.
Nish PatelCell Biology Program, The Hospital for Sick Children, Toronto, Canada.
Marc HildNovartis Institutes for BioMedical Research, Cambridge, United States.
Bosco LeungCell Biology Program, The Hospital for Sick Children, Toronto, Canada.
Zhengda LiDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, United States.
Yen-Chi ChenDepartment of Statistics, University of Washington, Seattle, United States.ORCID 0000-0002-4485-306X
Nancy ChangCell Biology Program, The Hospital for Sick Children, Toronto, Canada.
Yuan WangNovartis Institutes for BioMedical Research, Cambridge, United States.
Ceryl TanCell Biology Program, The Hospital for Sick Children, Toronto, Canada.
Shulamit DienaCell Biology Program, The Hospital for Sick Children, Toronto, Canada.
William TrimbleCell Biology Program, The Hospital for Sick Children, Toronto, Canada.
Larry WassermanDepartment of Statistics, Carnegie Mellon University, Pittsburgh, United States.
Jeremy L JenkinsNovartis Institutes for BioMedical Research, Cambridge, United States.
Marc W KirschnerDepartment of Systems Biology, Harvard Medical School, Boston, United States.ORCID 0000-0001-6540-6130
Ran KafriCell Biology Program, The Hospital for Sick Children, Toronto, Canada.ORCID 0000-0002-9656-0189

Funding

BIOCHEMICAL STUDIES OF MITOSISR01GM026875 · NIGMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI KIRSCHNER, MARC WALLACE · 1985 to 2019
$18.2M
BIOCHEMICAL STUDIES OF MITOSISR37GM026875 · NIGMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI KIRSCHNER, MARC W · 1986 to 1995
–
CIHR FRN-343437NIGMS NIH HHS GM26875NIGMS NIH HHS R01 GM026875
6 · The paper itself

Abstract

Animal cells within a tissue typically display a striking regularity in their size. To date, the molecular mechanisms that control this uniformity are still unknown. We have previously shown that size uniformity in animal cells is promoted, in part, by size-dependent regulation of G1 length. To identify the molecular mechanisms underlying this process, we performed a large-scale small molecule screen and found that the p38 MAPK pathway is involved in coordinating cell size and cell cycle progression. Small cells display higher p38 activity and spend more time in G1 than larger cells. Inhibition of p38 MAPK leads to loss of the compensatory G1 length extension in small cells, resulting in faster proliferation, smaller cell size and increased size heterogeneity. We propose a model wherein the p38 pathway responds to changes in cell size and regulates G1 exit accordingly, to increase cell size uniformity.

Indexed as

Cell SizeG1 PhaseSignal TransductionCell LineEpithelial CellsHumansp38 Mitogen-Activated Protein KinasesSocial Control, Formalp38 Mitogen-Activated Protein Kinasescell biologycell cyclecell growth controlcell sizecomputational biologyhigh-content screeninghumanp38 MAPK pathwaysystems biology

Identifiers

PMID29595474
PMCPMC5876018

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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.