Evidence map›Paper›PMID 35053521›Full record

ReviewCancers2022

Decellularized Colorectal Cancer Matrices as Bioactive Scaffolds for Studying Tumor-Stroma Interactions.

Ângela Marques-Magalhães, Tânia Cruz, Ângela Margarida Costa, Diogo Estêvão, Elisabete Rios, Pedro Amoroso Canão, Sérgia Velho, Fátima Carneiro, Maria José Oliveira, Ana Patrícia Cardoso

Abstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–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

18 citing papers in PubMed.

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  12. Iron metabolism in colorectal cancer: a balancing act.Cellular oncology (Dordrecht, Netherlands) · 2023
    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

10 authors.

Ângela Marques-Magalhãesi3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0000-0001-8961-5324
Tânia Cruzi3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.
Ângela Margarida Costai3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.
Diogo Estêvãoi3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0000-0001-6457-2356
Elisabete Riosi3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.
Pedro Amoroso CanãoDepartment of Pathology, Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal.
Sérgia Velhoi3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.
Fátima Carneiroi3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0000-0002-1964-1006
Maria José Oliveirai3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0000-0002-0724-0272
Ana Patrícia Cardosoi3S-Institute for Research and Innovation in Health, University of Porto, 4200-135 Porto, Portugal.ORCID 0000-0003-1987-0316

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

More than a physical structure providing support to tissues, the extracellular matrix (ECM) is a complex and dynamic network of macromolecules that modulates the behavior of both cancer cells and associated stromal cells of the tumor microenvironment (TME). Over the last few years, several efforts have been made to develop new models that accurately mimic the interconnections within the TME and specifically the biomechanical and biomolecular complexity of the tumor ECM. Particularly in colorectal cancer, the ECM is highly remodeled and disorganized and constitutes a key component that affects cancer hallmarks, such as cell differentiation, proliferation, angiogenesis, invasion and metastasis. Therefore, several scaffolds produced from natural and/or synthetic polymers and ceramics have been used in 3D biomimetic strategies for colorectal cancer research. Nevertheless, decellularized ECM from colorectal tumors is a unique model that offers the maintenance of native ECM architecture and molecular composition. This review will focus on innovative and advanced 3D-based models of decellularized ECM as high-throughput strategies in colorectal cancer research that potentially fill some of the gaps between in vitro 2D and in vivo models. Our aim is to highlight the need for strategies that accurately mimic the TME for precision medicine and for studying the pathophysiology of the disease.

Indexed as

colorectal cancerextracellular matrixpatient-derived scaffolds

Identifiers

PMID35053521
PMCPMC8773780

What OpenQuestion holds

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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.