Evidence map›Paper›PMID 23748611›Full record

ArticleNature cell biology2013

A screen for morphological complexity identifies regulators of switch-like transitions between discrete cell shapes.

Zheng Yin, Amine Sadok, Heba Sailem, Afshan McCarthy, Xiaofeng Xia, Fuhai Li, Mar Arias Garcia, Louise Evans, Alexis R Barr, Norbert Perrimon and 3 more

Abstract read
In one paragraph

Article in Nature cell biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing 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

105 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Systematic data analysis pipeline for quantitative morphological cell phenotyping.Computational and structural biotechnology journal · 2024
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Cell state transitions: catch them if you can.Development (Cambridge, England) · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

45 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Zheng YinNCI Center for Modeling Cancer Development, The Methodist Hospital Research Institute, Weill Cornell Medical College, 6670 Bertner Avenue, R6 South, Houston, Texas 77030, USA.
Amine Sadok
Heba Sailem
Afshan McCarthy
Xiaofeng Xia
Fuhai Li
Mar Arias Garcia
Louise Evans
Alexis R Barr
Norbert Perrimon
Christopher J Marshall
Stephen T C Wong
Chris Bakal

Funding

New collections of dsRNAs and overexpression miRNA constructs to supplement RNAiR01GM067761 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI PERRIMON, NORBERT · 2003 to 2019
$15.5M
The Core of the Computational BiologyU54CA149196 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WONG, STEPHEN TC · 2010 to 2015
$10.6M
Network analysis of Signal TransductionR01DK088718 · NIDDK · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2010 to 2014
$2.5M
High-content Image Analysis and Modeling for RANigenome-wide ScreeningR01CA121225 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI WONG, STEPHEN TC · 2008 to 2011
$1.2M
Cancer Research UK 13478Cancer Research UK 16512Cancer Research UK A13478Cancer Research UK C107/A10433Howard Hughes Medical InstituteNCI NIH HHS R01CA121225NCI NIH HHS U54 CA149196NCI NIH HHS U54CA149196NIDDK NIH HHS R01 DK088718NIGMS NIH HHS R01 GM067761Wellcome Trust 088452
6 · The paper itself

Abstract

The way in which cells adopt different morphologies is not fully understood. Cell shape could be a continuous variable or restricted to a set of discrete forms. We developed quantitative methods to describe cell shape and show that Drosophila haemocytes in culture are a heterogeneous mixture of five discrete morphologies. In an RNAi screen of genes affecting the morphological complexity of heterogeneous cell populations, we found that most genes regulate the transition between discrete shapes rather than generating new morphologies. In particular, we identified a subset of genes, including the tumour suppressor PTEN, that decrease the heterogeneity of the population, leading to populations enriched in rounded or elongated forms. We show that these genes have a highly conserved function as regulators of cell shape in both mouse and human metastatic melanoma cells.

Indexed as

Cell ShapeGenes, Tumor SuppressorGenetic TestingRNA InterferenceAnimalsDrosophila melanogasterHumansMelanomaMicePhenotypePTEN PhosphohydrolaseTumor Cells, CulturedPTEN Phosphohydrolase

Identifiers

PMID23748611
PMCPMC3712499

What OpenQuestion holds

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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.