Evidence map›Paper›PMID 33008910›Full record

ArticleScience advances2020

Peptide-protein coassembling matrices as a biomimetic 3D model of ovarian cancer.

Clara Louise Hedegaard, Carlos Redondo-Gómez, Bee Yi Tan, Kee Woei Ng, Daniela Loessner, Alvaro Mata

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.0field-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

34 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Biomimetic Scaffold-Based 3D Models for Decoding Cancer Biology and Advancing Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  17. Making In Vitro Tumor Models Whole Again.Advanced healthcare materials · 2023
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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

6 authors at 4 institutions in 4 countries.

Clara Louise HedegaardSchool of Engineering and Materials Science, Queen Mary University of London, Mile End Road, E1 4NS London, UK.ORCID 0000-0003-3096-1980
Carlos Redondo-GómezSchool of Engineering and Materials Science, Queen Mary University of London, Mile End Road, E1 4NS London, UK.ORCID 0000-0002-6610-5652
Bee Yi TanSchool of Materials Science and Engineering, Nanyang Technological University, Singapore 639798, Singapore.
Kee Woei NgSchool of Materials Science and Engineering, Nanyang Technological University, Singapore 639798, Singapore.ORCID 0000-0002-7276-3563
Daniela LoessnerCentre for Tumour Microenvironment, Barts Cancer Institute, Queen Mary University of London, EC1M 6BQ London, UK.ORCID 0000-0001-5891-3441
Alvaro MataSchool of Engineering and Materials Science, Queen Mary University of London, Mile End Road, E1 4NS London, UK. a.mata@nottingham.ac.uk.ORCID 0000-0002-6739-9111
Queen Mary University of London · GBNanyang Technological University · SGNational Skin Centre · SGUniversity of Nottingham · GB

Funding

Medical Research Council MR/R015651/1
6 · The paper itself

Abstract

Bioengineered three-dimensional (3D) matrices expand our experimental repertoire to study tumor growth and progression in a biologically relevant, yet controlled, manner. Here, we used peptide amphiphiles (PAs) to coassemble with and organize extracellular matrix (ECM) proteins producing tunable 3D models of the tumor microenvironment. The matrix was designed to mimic physical and biomolecular features of tumors present in patients. We included specific epitopes, PA nanofibers, and ECM macromolecules for the 3D culture of human ovarian cancer, endothelial, and mesenchymal stem cells. The multicellular constructs supported the formation of tumor spheroids with extensive F-actin networks surrounding the spheroids, enabling cell-cell communication, and comparative cell-matrix interactions and encapsulation response to those observed in Matrigel. We conducted a proof-of-concept study with clinically used chemotherapeutics to validate the functionality of the multicellular constructs. Our study demonstrates that peptide-protein coassembling matrices serve as a defined model of the multicellular tumor microenvironment of primary ovarian tumors.

Indexed as

BiomimeticsOvarian NeoplasmsCell Line, TumorExtracellular MatrixHumansPeptidesTumor MicroenvironmentPeptides

Identifiers

PMID33008910
PMCPMC7852381
OpenAlexW3091301386

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.