Evidence map›Paper›PMID 31311174›Full record

ArticleCancers2019

The Interplay between Colon Cancer Cells and Tumour-Associated Stromal Cells Impacts the Biological Clock and Enhances Malignant Phenotypes.

Luise Fuhr, Mónica Abreu, Annalucia Carbone, Rukeia El-Athman, Fabrizio Bianchi, Mikko O Laukkanen, Gianluigi Mazzoccoli, Angela Relógio

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

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  19. CBX4 Provides an Alternate Mode of Colon Cancer DevelopmentFrontiers in cell and developmental biology · 2021
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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 2 countries.

Luise FuhrInstitute for Theoretical Biology (ITB), Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, 10117 Berlin, Germany.
Mónica AbreuInstitute for Theoretical Biology (ITB), Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, 10117 Berlin, Germany.
Annalucia CarboneDivision of Internal Medicine and Chronobiology Unit, Fondazione IRCCS (Istituto di Ricerca a Carattere Clinico e Scientifico) Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo (FG), Italy.
Rukeia El-AthmanInstitute for Theoretical Biology (ITB), Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, 10117 Berlin, Germany.
Fabrizio BianchiUnit of Oncology Biomarkers, Fondazione IRCCS (Istituto di Ricerca a Carattere Clinico e Scientifico) Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo (FG), Italy.
Mikko O LaukkanenResearch laboratory, Pineta Grande, 80131 Caserta, Italy.
Gianluigi MazzoccoliDivision of Internal Medicine and Chronobiology Unit, Fondazione IRCCS (Istituto di Ricerca a Carattere Clinico e Scientifico) Casa Sollievo della Sofferenza, 71013 San Giovanni Rotondo (FG), Italy. g.mazzoccoli@operapadrepio.it.
Angela RelógioInstitute for Theoretical Biology (ITB), Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, 10117 Berlin, Germany. angela.relogio@charite.de.
Humboldt-Universität zu Berlin · DECasa Sollievo della Sofferenza · ITVilla Pineta Hospital · IT

Funding

"5x1000" voluntary contributionBerlin School of Integrative Oncology (BSIO) Charité - Universitätsmedizin BerlinDr. R. Schwiete Stiftung 09/2017German Federal Ministry of Education and Research (BMBF) eBio-CIRSPLICE - FKZ031A316Ricerca Corrente 2019
6 · The paper itself

Abstract

Cancer cells interrelate with the bordering host microenvironment that encompasses the extracellular matrix and a nontumour cellular component comprising fibroblasts and immune-competent cells. The tumour microenvironment modulates cancer onset and progression, but the molecular factors managing this interaction are not fully understood. Malignant transformation of a benign tumour is among the first crucial events in colorectal carcinogenesis. The role of tumour stroma fibroblasts is well-described in cancer, but less well-characterized in benign tumours. In the current work we utilized fibroblasts isolated from tubulovillous adenoma, which has high risk for malignant transformation, to study the interaction between benign tumour stroma and the circadian clock machinery. We explored the role of the biological clock in this interplay taking advantage of an experimental model, represented by the co-culture of colon cancer cells with normal fibroblasts or tumour-associated fibroblasts, isolated from human colorectal tumour specimens. When co-cultured with tumour-associated fibroblasts, colon cancer cells showed alterations in their circadian and metabolic parameters, with decreased apoptosis, increased colon cancer cell viability, and increased resistance to chemotherapeutic agents. In conclusion, the interactions among colon cancer cells and tumour-associated fibroblasts affect the molecular clockwork and seem to aggravate malignant cell phenotypes, suggesting a detrimental effect of this interplay on cancer dynamics.

Indexed as

biological clockcancercolorectaltumour stroma

Identifiers

PMID31311174
PMCPMC6678177
OpenAlexW2959761191

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.