Evidence map›Paper›PMID 19603013›Full record

ArticleBritish journal of cancer2009

Newly characterised ex vivo colospheres as a three-dimensional colon cancer cell model of tumour aggressiveness.

L-B Weiswald, S Richon, P Validire, M Briffod, R Lai-Kuen, F P Cordelières, F Bertrand, D Dargere, G Massonnet, E Marangoni and 6 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

43 citing papers in PubMed, 78 citations in OpenAlex.

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  15. Overcoming biological barriers to improve solid tumor immunotherapy.Drug delivery and translational research · 2021
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  16. 3D Tumor Spheroid Models for In Vitro Therapeutic Screening of Nanoparticles.Advances in experimental medicine and biology · 2021
    Article
  17. Review
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  19. UNR/Journal of clinical medicine · 2019
    Article
  20. Article
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

16 authors at 6 institutions in 1 country.

L-B WeiswaldIFR71 Sciences du Médicament, Faculté des Sciences Pharmaceutiques et Biologiques, Université Paris Descartes, 4 avenue de l'Observatoire, F-75006 Paris, France.
S Richon
P Validire
M Briffod
R Lai-Kuen
F P Cordelières
F Bertrand
D Dargere
G Massonnet
E Marangoni
B Gayet
M Pocard
I Bieche
M-F Poupon
D Bellet
V Dangles-Marie
Délégation Paris 5 · FRHôpital René Huguenin · FRInstitut Curie · FRUniversité Paris Cité · FRInserm · FRInstitute Mutualiste Montsouris · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNew models continue to be required to improve our understanding of colorectal cancer progression. To this aim, we characterised in this study a three-dimensional multicellular tumour model that we named colospheres, directly obtained from mechanically dissociated colonic primary tumours and correlated with metastatic potential.

methodsColorectal primary tumours (n=203) and 120 paired non-tumoral colon mucosa were mechanically disaggregated into small fragments for short-term cultures. Features of tumours producing colospheres were analysed. Further characterisation was performed using colospheres, generated from a human colon cancer xenograft, and spheroids, formed on agarose by the paired cancer cell lines.

resultsColospheres, exclusively formed by viable cancer cells, were obtained in only 1 day from 98 tumours (47%). Inversely, non-tumoral colonic mucosa never generated colospheres. Colosphere-forming capacity was statistically significantly associated with tumour aggressiveness, according to AJCC stage analysis. Despite a close morphology, colospheres displayed higher invasivity than did spheroids. Spheroids and colospheres migrated into Matrigel but matrix metalloproteinase (MMP)-2 and MMP-9 activity was detected only in colospheres. Mouse subrenal capsule assay revealed the unique tumorigenic and metastatic phenotype of colospheres. Moreover, colospheres and parental xenograft reproduced similar CD44 and CD133 expressions in which CD44+ cells represented a minority subset of the CD133+ population.

conclusionThe present colospheres provide an ex vivo three-dimensional model, potentially useful for studying metastatic process.

Indexed as

AC133 AntigenAnimalsAntigens, CDCell Line, TumorCell MovementColorectal NeoplasmsFemaleGlycoproteinsHumansMiceNeoplasm InvasivenessNeoplastic Stem CellsPeptidesSpheroids, CellularAC133 AntigenAntigens, CDGlycoproteinsPeptidesPROM1 protein, humanProm1 protein, mouse

Identifiers

PMID19603013
PMCPMC2720229
OpenAlexW2090259160

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.