Evidence map›Paper›PMID 38307492›Full record

ReviewCellular and molecular gastroenterology and hepatology2024

Fibroblasts in Orchestrating Colorectal Tumorigenesis and Progression.

Subinuer Abudukelimu, Noel F C C de Miranda, Lukas J A C Hawinkels

Open access · goldAbstract readReview
In one paragraph

Review in Cellular and molecular gastroenterology and hepatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.9field-weighted citation impact, top 3% 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, 21 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Subinuer AbudukelimuDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
Noel F C C de MirandaDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Lukas J A C HawinkelsDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands. Electronic address: l.j.a.c.hawinkels@lumc.nl.
Leiden University Medical Center · NL

Funding

European Research Council 852832
6 · The paper itself

Abstract

Cancer-associated fibroblasts (CAFs) are an abundant component of the tumor microenvironment and have been shown to possess critical functions in tumor progression. Although their roles predominantly have been described as tumor-promoting, more recent findings have identified subsets of CAFs with tumor-restraining functions. Accumulating evidence underscores large heterogeneity in fibroblast subsets in which distinct subsets differentially impact the initiation, progression, and metastasis of colorectal cancer. In this review, we summarize and discuss the evolving role of CAFs in colorectal cancer, highlighting the ongoing controversies regarding their distinct origins and multifaceted functions. In addition, we explore how CAFs can confer resistance to current therapies and the challenges of developing effective CAF-directed therapies. Taken together, we believe that, in this rapidly evolving field, it is crucial first to understand CAF dynamics comprehensively, and to bridge existing knowledge gaps regarding CAF heterogeneity and plasticity before further exploring the clinical targeting of CAFs.

Indexed as

Cancer-Associated FibroblastsColorectal NeoplasmsCarcinogenesisCell Transformation, NeoplasticFibroblastsHumansTumor MicroenvironmentAdenoma-to-Carcinoma TransitionCancer-Associated FibroblastColorectal CancerHeterogeneity

Identifiers

PMID38307492
PMCPMC10966773
OpenAlexW4391482025

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.