Evidence map›Paper›PMID 33635003›Full record

ReviewClinical and translational medicine2021

Understanding cell-cell communication and signaling in the colorectal cancer microenvironment.

Shaikha AlMusawi, Mehreen Ahmed, Abdolrahman S Nateri

Abstract readReview
In one paragraph

Review in Clinical and translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed, 1 pooled it
–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

89 citing papers in PubMed, 1 synthesis or guideline pooled it.

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29 more citing papers are in PubMed but not listed here.

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

3 authors.

Shaikha AlMusawiCancer Genetics & Stem Cell Group, BioDiscovery Institute, Division of Cancer & Stem Cells, School of Medicine, University of Nottingham, Nottingham, UK.
Mehreen AhmedCancer Genetics & Stem Cell Group, BioDiscovery Institute, Division of Cancer & Stem Cells, School of Medicine, University of Nottingham, Nottingham, UK.
Abdolrahman S NateriCancer Genetics & Stem Cell Group, BioDiscovery Institute, Division of Cancer & Stem Cells, School of Medicine, University of Nottingham, Nottingham, UK.ORCID 0000-0002-6422-6813

Funding

National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/P001793/1
6 · The paper itself

Abstract

Carcinomas are complex heterocellular systems containing epithelial cancer cells, stromal fibroblasts, and multiple immune cell-types. Cell-cell communication between these tumor microenvironments (TME) and cells drives cancer progression and influences response to existing therapies. In order to provide better treatments for patients, we must understand how various cell-types collaborate within the TME to drive cancer and consider the multiple signals present between and within different cancer types. To investigate how tissues function, we need a model to measure both how signals are transferred between cells and how that information is processed within cells. The interplay of collaboration between different cell-types requires cell-cell communication. This article aims to review the current in vitro and in vivo mono-cellular and multi-cellular cultures models of colorectal cancer (CRC), and to explore how they can be used for single-cell multi-omics approaches for isolating multiple types of molecules from a single-cell required for cell-cell communication to distinguish cancer cells from normal cells. Integrating the existing single-cell signaling measurements and models, and through understanding the cell identity and how different cell types communicate, will help predict drug sensitivities in tumor cells and between- and within-patients responses.

Indexed as

AnimalsCell CommunicationCell Culture TechniquesColorectal NeoplasmsDrosophilaHumansMiceSignal TransductionTumor MicroenvironmentCellPhoneDBCITE-seqColorectal cancer (CRC)CyTOFpatient-derived explant (PDE)patient-derived organoid (PDO)patient-derived xenografts (PDX)scRNA-seqTumor microenvironments (TME)

Identifiers

PMID33635003
PMCPMC7868082

What Socratic 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 Socratic graph.