Evidence map›Paper›PMID 33643799›Full record

ReviewAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2021

Proteinaceous Hydrogels for Bioengineering Advanced 3D Tumor Models.

Barbara Blanco-Fernandez, Vítor M Gaspar, Elisabeth Engel, João F Mano

Open access · goldAbstract readReview
In one paragraph

Review in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Pooled it
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  11. Revolutionizing bone healing: the role of 3D models.Cell regeneration (London, England) · 2025
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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

4 authors at 3 institutions in 2 countries.

Barbara Blanco-FernandezDepartment of Chemistry, CICECO - Aveiro Institute of Materials, University of Aveiro Campus Universitário de Santiago Aveiro 3810-193 Portugal.ORCID https://orcid.org/0000-0001-5050-9663
Vítor M GasparDepartment of Chemistry, CICECO - Aveiro Institute of Materials, University of Aveiro Campus Universitário de Santiago Aveiro 3810-193 Portugal.ORCID https://orcid.org/0000-0002-0372-2493
Elisabeth EngelInstitute for Bioengineering of Catalonia (IBEC) The Barcelona Institute of Science and Technology Baldiri Reixac 10-12 Barcelona 08028 Spain.ORCID https://orcid.org/0000-0003-4855-8874
João F ManoDepartment of Chemistry, CICECO - Aveiro Institute of Materials, University of Aveiro Campus Universitário de Santiago Aveiro 3810-193 Portugal.ORCID https://orcid.org/0000-0002-2342-3765
University of Aveiro · PTBiomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine · ESInstitute for Bioengineering of Catalonia · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The establishment of tumor microenvironment using biomimetic in vitro models that recapitulate key tumor hallmarks including the tumor supporting extracellular matrix (ECM) is in high demand for accelerating the discovery and preclinical validation of more effective anticancer therapeutics. To date, ECM-mimetic hydrogels have been widely explored for 3D in vitro disease modeling owing to their bioactive properties that can be further adapted to the biochemical and biophysical properties of native tumors. Gathering on this momentum, herein the current landscape of intrinsically bioactive protein and peptide hydrogels that have been employed for 3D tumor modeling are discussed. Initially, the importance of recreating such microenvironment and the main considerations for generating ECM-mimetic 3D hydrogel in vitro tumor models are showcased. A comprehensive discussion focusing protein, peptide, or hybrid ECM-mimetic platforms employed for modeling cancer cells/stroma cross-talk and for the preclinical evaluation of candidate anticancer therapies is also provided. Further development of tumor-tunable, proteinaceous or peptide 3D microtesting platforms with microenvironment-specific biophysical and biomolecular cues will contribute to better mimic the in vivo scenario, and improve the predictability of preclinical screening of generalized or personalized therapeutics.

Indexed as

3D in vitro modelscancershydrogelspeptidesproteins

Identifiers

PMID33643799
PMCPMC7887602
OpenAlexW3119032156

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.