Evidence map›Paper›PMID 33924238›Full record

ArticleInternational journal of molecular sciences2021

Tissue-Engineering the Fibrous Pancreatic Tumour Stroma Capsule in 3D Tumouroids to Demonstrate Paclitaxel Response.

Judith Pape, Katerina Stamati, Rawiya Al Hosni, Ijeoma F Uchegbu, Andreas G Schatzlein, Marilena Loizidou, Mark Emberton, Umber Cheema

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 14 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

8 authors at 2 institutions in 1 country.

Judith PapeCentre for 3D Models of Health and Disease, Department of Targeted Intervention, Division of Surgery and Interventional Science, University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TS, UK.ORCID 0000-0002-4225-5568
Katerina StamatiResearch Department of Surgical Biotechnology, Division of Surgery and Interventional Sciences, University College London, Royal Free Hospital Campus, Rowland Hill Street, London NW3 2PF, UK.ORCID 0000-0003-1815-7076
Rawiya Al HosniCentre for 3D Models of Health and Disease, Department of Targeted Intervention, Division of Surgery and Interventional Science, University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TS, UK.ORCID 0000-0001-8803-4317
Ijeoma F UchegbuDepartment of Pharmaceutical and Biological Chemistry, School of Pharmacy, University College London, 29-39 Brunswick Square, London WC1N 1AX, UK.
Andreas G SchatzleinDepartment of Pharmaceutical and Biological Chemistry, School of Pharmacy, University College London, 29-39 Brunswick Square, London WC1N 1AX, UK.
Marilena LoizidouResearch Department of Surgical Biotechnology, Division of Surgery and Interventional Sciences, University College London, Royal Free Hospital Campus, Rowland Hill Street, London NW3 2PF, UK.ORCID 0000-0002-0900-9795
Mark EmbertonFaculty of Medical Sciences, University College London, Maple House, 149 Tottenham Court Road, London W1T 7TNF, UK.
Umber CheemaCentre for 3D Models of Health and Disease, Department of Targeted Intervention, Division of Surgery and Interventional Science, University College London, Charles Bell House, 43-45 Foley Street, London W1W 7TS, UK.ORCID 0000-0002-4366-3897
University College London · GBThe Royal Free Hospital · GB

Funding

EPSRC EP/M507970/1 Project Code: 524590
6 · The paper itself

Abstract

Pancreatic cancer is a unique cancer in that up to 90% of its tumour mass is composed of a hypovascular and fibrotic stroma. This makes it extremely difficult for chemotherapies to be delivered into the core of the cancer mass. We tissue-engineered a biomimetic 3D pancreatic cancer ("tumouroid") model comprised of a central artificial cancer mass (ACM), containing MIA Paca-2 cells, surrounded by a fibrotic stromal compartment. This stromal compartment had a higher concentration of collagen type I, fibronectin, laminin, and hyaluronic acid (HA) than the ACM. The incorporation of HA was validated with alcian blue staining. Response to paclitaxel was determined in 2D MIA Paca-2 cell cultures, the ACMs alone, and in simple and complex tumouroids, in order to demonstrate drug sensitivity within pancreatic tumouroids of increasing complexity. The results showed that MIA Paca-2 cells grew into the complex stroma and invaded as cell clusters with a maximum distance of 363.7 µm by day 21. In terms of drug response, the IC

Indexed as

Tissue EngineeringCell Line, TumorCell ProliferationDose-Response Relationship, DrugDrug Resistance, NeoplasmFluorescent Antibody TechniqueHumansImmunohistochemistryPaclitaxelPancreatic NeoplasmsSpheroids, CellularStromal CellsTumor Cells, CulturedTumor MicroenvironmentPaclitaxel3D tumour modelschemoresistancedesmoplasiahyaluronic acidpancreatic cancer

Identifiers

PMID33924238
PMCPMC8074746
OpenAlexW3153505444

What OpenQuestion holds

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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.