Evidence map›Paper›PMID 24746967›Full record

ArticleBiomaterials2014

Bioengineered human tumor within a bone niche.

Aranzazu Villasante, Alessandro Marturano-Kruik, Gordana Vunjak-Novakovic

Abstract read
In one paragraph

Article in Biomaterials, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 64 citations in OpenAlex.

  1. Exploring bone-tumor interactions through 3DJournal of bone oncology · 2025
    Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Engineering complexity in human tissue models of cancer.Advanced drug delivery reviews · 2022
    Review
  8. Article
  9. Article
  10. Journal of bone oncology · 2021
    Review
  11. Human Serum Enhances Biomimicry of Engineered Tissue Models of Bone and Cancer.Frontiers in bioengineering and biotechnology · 2021
    Article
  12. Article
  13. Article
  14. Modeling neoplastic disease with spheroids and organoids.Journal of hematology & oncology · 2020
    Review
  15. Review
  16. Tissue-Engineered Bone Tumor as a Reproducible Human in Vitro Model for Studies of Anticancer Drugs.Toxicological sciences : an official journal of the Society of Toxicology · 2020
    Article
  17. Review
  18. Review
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Aranzazu VillasanteDepartment of Biomedical Engineering, Columbia University, 622 West 168th Street, VC12-234, New York, NY 10032, USA. Electronic address: av2499@columbia.edu.
Alessandro Marturano-KruikDepartment of Biomedical Engineering, Columbia University, 622 West 168th Street, VC12-234, New York, NY 10032, USA. Electronic address: am3934@columbia.edu.
Gordana Vunjak-NovakovicDepartment of Biomedical Engineering, Columbia University, 622 West 168th Street, VC12-234, New York, NY 10032, USA. Electronic address: gv2131@columbia.edu.
Columbia University · US

Funding

Translational Bioreactors - Engineering Complex TissuesP41EB002520 · NIBIB · TUFTS UNIVERSITY MEDFORD · PI KAPLAN, DAVID L. · 2004 to 2018
$16.7M
NIBIB NIH HHS EB002520NIBIB NIH HHS P41 EB002520
6 · The paper itself

Abstract

Monolayer cultures of tumor cells and animal studies have tremendously advanced our understanding of cancer biology. However, we often lack animal models for human tumors, and cultured lines of human cells quickly lose their cancer signatures. In recent years, simple 3D models for cancer research have emerged, including cell culture in spheroids and on biomaterial scaffolds. Here we describe a bioengineered model of human Ewing's sarcoma that mimics the native bone tumor niche with high biological fidelity. In this model, cancer cells that have lost their transcriptional profiles after monolayer culture re-express genes related to focal adhesion and cancer pathways. The bioengineered model recovers the original hypoxic and glycolytic tumor phenotype, and enables re-expression of angiogenic and vasculogenic mimicry features that favor tumor adaptation. We propose that differentially expressed genes between the monolayer cell culture and native tumor environment are potential therapeutic targets that can be explored using the bioengineered tumor model.

Indexed as

AnimalsBone NeoplasmsCell Culture TechniquesCell Line, TumorGene Expression Regulation, NeoplasticGenetic EngineeringHEK293 CellsHumansSarcoma, EwingSpheroids, CellularTranscription, GeneticTumor Cells, CulturedTumor MicroenvironmentCancerEwing's sarcomaMicroenvironmentTherapeutic targetsTissue engineeringTumor niche

Identifiers

PMID24746967
PMCPMC4048837
OpenAlexW2049426260

What OpenQuestion holds

Textmetadata
LicenceTDM
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.