Evidence map›Paper›PMID 32232163›Full record

ArticleScience advances2020

Role of mechanical cues and hypoxia on the growth of tumor cells in strong and weak confinement: A dual in vitro-in silico approach.

V Le Maout, K Alessandri, B Gurchenkov, H Bertin, P Nassoy, G Sciumè

Abstract read
In one paragraph

Article in Science advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. The Applications and Challenges of the Development ofCellular and molecular bioengineering · 2023
    Review
  6. Article
  7. Review
  8. 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

6 authors.

V Le MaoutI2M, Institute of Mechanics and Mechanical Engineering, Univ. Bordeaux, CNRS, ENSAM, Bordeaux INP, Talence, France.ORCID 0000-0002-2366-1632
K AlessandriLP2N, Laboratoire Photonique Numérique et Nanosciences, Univ. Bordeaux, F-33400 Talence, France.ORCID 0000-0002-1986-3493
B GurchenkovInstitut du Cerveau et de la Moëlle épinière (ICM), INSERM U 1127, CNRS UMR 7225, Sorbonne Université, F-75013 Paris, France.
H BertinI2M, Institute of Mechanics and Mechanical Engineering, Univ. Bordeaux, CNRS, ENSAM, Bordeaux INP, Talence, France.
P NassoyLP2N, Laboratoire Photonique Numérique et Nanosciences, Univ. Bordeaux, F-33400 Talence, France.ORCID 0000-0003-4615-9431
G SciumèI2M, Institute of Mechanics and Mechanical Engineering, Univ. Bordeaux, CNRS, ENSAM, Bordeaux INP, Talence, France.ORCID 0000-0001-5231-7374

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Characterization of tumor growth dynamics is of major importance for cancer understanding. By contrast with phenomenological approaches, mechanistic modeling can facilitate disclosing underlying tumor mechanisms and lead to identification of physical factors affecting proliferation and invasive behavior. Current mathematical models are often formulated at the tissue or organ scale with the scope of a direct clinical usefulness. Consequently, these approaches remain empirical and do not allow gaining insight into the tumor properties at the scale of small cell aggregates. Here, experimental and numerical studies of the dynamics of tumor aggregates are performed to propose a physics-based mathematical model as a general framework to investigate tumor microenvironment. The quantitative data extracted from the cellular capsule technology microfluidic experiments allow a thorough quantitative comparison with in silico experiments. This dual approach demonstrates the relative impact of oxygen and external mechanical forces during the time course of tumor model progression.

Indexed as

Mechanical PhenomenaModels, TheoreticalAlgorithmsHumansHypoxiaNeoplasms

Identifiers

PMID32232163
PMCPMC7096162

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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.