Evidence map›Paper›PMID 34359593›Full record

ArticleCancers2021

Is There

Antoine M Dujon, Jean-Pascal Capp, Joel S Brown, Pascal Pujol, Robert A Gatenby, Beata Ujvari, Catherine Alix-Panabières, Frédéric Thomas

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
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

20 citing papers in PubMed, 38 citations in OpenAlex.

  1. The Pro-Metastatic Roles of ROS.Antioxidants (Basel, Switzerland) · 2026
    Review
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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

8 authors at 3 institutions in 3 countries.

Antoine M DujonCREEC/CANECEV, MIVEGEC (CREES), University of Montpellier, CNRS, IRD, 34172 Montpellier, France.ORCID 0000-0002-1579-9156
Jean-Pascal CappToulouse Biotechnology Institute, INSA, CNRS, INRAE, University of Toulouse, 31555 Toulouse, France.ORCID 0000-0002-6470-079X
Joel S BrownDepartment of Integrated Mathematical Oncology, Moffitt Cancer Center, Tampa, FL 33601, USA.
Pascal PujolCREEC/CANECEV, MIVEGEC (CREES), University of Montpellier, CNRS, IRD, 34172 Montpellier, France.ORCID 0000-0001-8315-4715
Robert A GatenbyDepartment of Integrated Mathematical Oncology, Moffitt Cancer Center, Tampa, FL 33601, USA.
Beata UjvariCentre for Integrative Ecology, School of Life and Environmental Sciences, Deakin University, Waurn Ponds, VIC 3216, Australia.
Catherine Alix-PanabièresCREEC/CANECEV, MIVEGEC (CREES), University of Montpellier, CNRS, IRD, 34172 Montpellier, France.ORCID 0000-0002-6401-2903
Frédéric ThomasCREEC/CANECEV, MIVEGEC (CREES), University of Montpellier, CNRS, IRD, 34172 Montpellier, France.ORCID 0000-0003-2238-1978
Centre National de la Recherche Scientifique · FRMoffitt Cancer Center · USUniversity of Tasmania · AU

Funding

ERA-NET EU/TRANSCAN 2 JTC 2016 PROLIPSYMarie Skłodowska-Curie 765492SIRIC Montpellier Cancer Grant INCa_Inserm_DGOS_12553
6 · The paper itself

Abstract

The majority of cancer-related deaths are the result of metastases (i.e., dissemination and establishment of tumor cells at distant sites from the origin), which develop through a multi-step process classically termed the metastatic cascade. The respective contributions of each step to the metastatic process are well described but are also currently not completely understood. Is there, for example, a critical phase that disproportionately affects the probability of the development of metastases in individual patients? Here, we address this question using a modified Drake equation, initially formulated by the astrophysicist Frank Drake to estimate the probability of the emergence of intelligent civilizations in the Milky Way. Using simulations based on realistic parameter values obtained from the literature for breast cancer, we examine, under the linear progression hypothesis, the contribution of each component of the metastatic cascade. Simulations demonstrate that the most critical parameter governing the formation of clinical metastases is the survival duration of circulating tumor cells (CTCs).

Indexed as

circulating tumor cellsDrake equationmetastasismetastatic process

Identifiers

PMID34359593
PMCPMC8345184
OpenAlexW3184021749

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.