Evidence map›Paper›PMID 26133367›Full record

ReviewTheoretical biology & medical modelling2015

Proposal of a hybrid approach for tumor progression and tumor-induced angiogenesis.

Patricio Cumsille, Aníbal Coronel, Carlos Conca, Cristóbal Quiñinao, Carlos Escudero

Abstract readReview
In one paragraph

Review in Theoretical biology & medical modelling, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. The Antitumor Activities ofFrontiers in oncology · 2018
    Review
  10. Review
  11. 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

5 authors.

Patricio CumsilleDepartment of Basic Sciences, Faculty of Sciences, Universidad del Bío-Bío, Campus Fernando May, Av. Andrés Bello s/n, Casilla 447 Chillán, Chile. pcumsille@ubiobio.cl.
Aníbal CoronelDepartment of Basic Sciences, Faculty of Sciences, Universidad del Bío-Bío, Campus Fernando May, Av. Andrés Bello s/n, Casilla 447 Chillán, Chile. acoronel@ubiobio.cl.
Carlos ConcaCentre for Biotechnology and Bioengineering, University of Chile, Beaucheff 851, Santiago, Chile. cconca@dim.uchile.cl.
Cristóbal QuiñinaoLaboratoire Jacques-Louis Lions, Université Pierre et Marie Curie and Mathematical Neuroscience Team, CIRB, Collège de France, (UMR CNRS 7598), 4 place de Jussieu, Paris, F-75005, France. cristobal.quininao@college-de-france.fr.
Carlos EscuderoDepartment of Basic Sciences, Faculty of Sciences, Universidad del Bío-Bío, Campus Fernando May, Av. Andrés Bello s/n, Casilla 447 Chillán, Chile. cescudero@ubiobio.cl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the main challenges in cancer modelling is to improve the knowledge of tumor progression in areas related to tumor growth, tumor-induced angiogenesis and targeted therapies efficacy. For this purpose, incorporate the expertise from applied mathematicians, biologists and physicians is highly desirable. Despite the existence of a very wide range of models, involving many stages in cancer progression, few models have been proposed to take into account all relevant processes in tumor progression, in particular the effect of systemic treatments and angiogenesis. Composite biological experiments, both in vitro and in vivo, in addition with mathematical modelling can provide a better understanding of theses aspects. In this work we proposed that a rational experimental design associated with mathematical modelling could provide new insights into cancer progression. To accomplish this task, we reviewed mathematical models and cancer biology literature, describing in detail the basic principles of mathematical modelling. We also analyze how experimental data regarding tumor cells proliferation and angiogenesis in vitro may fit with mathematical modelling in order to reconstruct in vivo tumor evolution. Additionally, we explained the mathematical methodology in a comprehensible way in order to facilitate its future use by the scientific community.

Indexed as

Neovascularization, PathologicHumansModels, BiologicalNeoplasms

Identifiers

PMID26133367
PMCPMC4509478

What OpenQuestion holds

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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.