Evidence map›Paper›PMID 32155897›Full record

ArticleInternational journal of molecular sciences2020

In Vitro Vascular Network Modified to Function as Culture Platform and Angiogenic Induction Potential Test for Cancer Cells.

Outi Huttala, Synnöve Staff, Tuula Heinonen, Johanna Mäenpää, Minna Tanner, Timo Ylikomi

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Medicinal Plant-rich Diet: A Potential Therapeutic Role in Colorectal Cancer.Cardiovascular & hematological agents in medicinal chemistry · 2024
    Review
  2. Article
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 2 institutions in 1 country.

Outi HuttalaCell Biology, Faculty of Medicine and Health Technology, Tampere University, FI-33014 Tampere, Finland.ORCID 0000-0002-9052-7230
Synnöve StaffTays Cancer Center, Tampere University Hospital, FI-33520 Tampere, Finland.
Tuula HeinonenFICAM, Faculty of Medicine and Health Technology, Tampere University, FI-33014 Tampere, Finland.
Johanna MäenpääTays Cancer Center, Tampere University Hospital, FI-33520 Tampere, Finland.
Minna TannerTays Cancer Center, Tampere University Hospital, FI-33520 Tampere, Finland.
Timo YlikomiCell Biology, Faculty of Medicine and Health Technology, Tampere University, FI-33014 Tampere, Finland.
Tampere University · FITampere University Hospital · FI

Funding

Business Finland Dnro 3985/31/15City of Tampere Science Foundation 2017Juliana von Wendtin Säätiö 2018
6 · The paper itself

Abstract

Drug treatments have been designed to inhibit tumor angiogenesis in hope of stopping tumor growth. However, not all tumor types respond to this type of treatment. A screening method which identifies angiogenesis inducing cancer types would help predict the efficacy of angiogenesis-inhibiting drugs for the patients. Our goal is to develop (1) a cell assay to assess the angiogenic induction potential of patient-derived tumor cells, and (2) a protocol for culturing cancer cells on a vascular platform. We optimized the media composition and seeding density of cells (hASC, HUVEC, and cancer cells) to 48-, 96-, and even 384-well plate sizes to allow vascular formation and cancer cell proliferation and subsequent analysis with high throughput. The angiogenic induction potential of patient-derived cancer cells was investigated by quantifying the formation of tubular structures and the drug response of cancer cells grown on a vascular platform was evaluated using gene expression and cell viability (WST-1) assay. Immunocytochemistry was performed with von Willebrand factor, collagen IV, CD44, cytokeratin 19 and ALDH1A1. The angiogenic induction potential test was shown to be responsive to the induction of angiogenesis by cancer cells. The responses of cancer cells were different when grown on a vascular platform or on plastic, seen in gene expression level and viability results. These two protocols are promising novel tools for aiding the selection of efficient cancer drugs for personalized medicine and as an alternative cancer cell culture platform.

Indexed as

Cell MovementCell ProliferationNeovascularization, PathologicNeovascularization, PhysiologicBiological AssayCells, CulturedCoculture TechniquesHumansHuman Umbilical Vein Endothelial CellsIn Vitro TechniquesMesenchymal Stem CellsNeoplasmsangiogenesiscancerfunctional assayhuman adipose stromal cellshuman umbilical vein endothelial cellsin vitro assaypatient-derived cancer cellspatient-specificpersonalized medicine

Identifiers

PMID32155897
PMCPMC7084873
OpenAlexW3009600816

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.