Evidence map›Paper›PMID 23363630›Full record

ReviewProceedings. Biological sciences2013

Cutting through the complexity of cell collectives.

Carey D Nadell, Vanni Bucci, Knut Drescher, Simon A Levin, Bonnie L Bassler, João B Xavier

Abstract readReview
In one paragraph

Review in Proceedings. Biological sciences, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing 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

71 citing papers in PubMed.

  1. Temperate phages limit their own propagation under spatial constraint in biofilms on chitin.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. Multiplicity of type 6 secretion system toxins limits the evolution of resistance.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Open problems in synthetic multicellularity.NPJ systems biology and applications · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Fluid flow structures gut microbiota biofilm communities by distributing public goods.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  11. Article
  12. Review
  13. Morphological instability and roughening of growing 3D bacterial colonies.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  14. Social evolution of shared biofilm matrix components.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Tempos and modes of collectivity in the history of life.Theory in biosciences = Theorie in den Biowissenschaften · 2021
    Review
  20. Article

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

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

6 authors.

Carey D NadellDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA. cnadell@princeton.edu
Vanni Bucci
Knut Drescher
Simon A Levin
Bonnie L Bassler
João B Xavier

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Elisa de Stanchina · 1985 to 2026
$347.4M
Variability of Cellular Responses to Growth Factors and Drugs During TumorgenesisU54CA148967 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SANDER, CHRIS · 2010 to 2014
$13.8M
Intra-and Inter-Species Communication in BacteriaR01GM065859 · NIGMS · PRINCETON UNIVERSITY · PI BASSLER, BONNIE L · 2002 to 2015
$4.2M
Engineering microbial social interactions: Towards new anti-biofilm therapiesDP2OD008440 · OD · SLOAN-KETTERING INST CAN RESEARCH · PI XAVIER, JOAO · 2011 to 2015
$2.9M
Howard Hughes Medical InstituteNCI NIH HHS 1-U54-CA148967-01NCI NIH HHS P30 CA008748NCI NIH HHS U54 CA148967NIGMS NIH HHS 5R01GM065859NIGMS NIH HHS R01 GM065859NIH HHS DP2 OD008440NIH HHS DP2OD008440
6 · The paper itself

Abstract

Via strength in numbers, groups of cells can influence their environments in ways that individual cells cannot. Large-scale structural patterns and collective functions underpinning virulence, tumour growth and bacterial biofilm formation are emergent properties of coupled physical and biological processes within cell groups. Owing to the abundance of factors influencing cell group behaviour, deriving general principles about them is a daunting challenge. We argue that combining mechanistic theory with theoretical ecology and evolution provides a key strategy for clarifying how cell groups form, how they change in composition over time, and how they interact with their environments. Here, we review concepts that are critical for dissecting the complexity of cell collectives, including dimensionless parameter groups, individual-based modelling and evolutionary theory. We then use this hybrid modelling approach to provide an example analysis of the evolution of cooperative enzyme secretion in bacterial biofilms.

Indexed as

Bacterial Physiological PhenomenaBiofilmsSelection, GeneticBacteriaBiological EvolutionModels, BiologicalQuorum Sensing

Identifiers

PMID23363630
PMCPMC3574390

What OpenQuestion holds

Textmetadata
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.