Evidence map›Paper›PMID 23576741›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Modeling Ewing sarcoma tumors in vitro with 3D scaffolds.

Eliza Li Shan Fong, Salah-Eddine Lamhamedi-Cherradi, Emily Burdett, Vandhana Ramamoorthy, Alexander J Lazar, F Kurtis Kasper, Mary C Farach-Carson, Deeksha Vishwamitra, Elizabeth G Demicco, Brian A Menegaz and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed
15.2field-weighted citation impact, top 1% 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

105 citing papers in PubMed, 240 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Exploring bone-tumor interactions through 3DJournal of bone oncology · 2025
    Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Small round cell sarcomas.Nature reviews. Disease primers · 2022
    Review
  19. Review
  20. Multiple Cell Cultures for MRI Analysis.International journal of molecular sciences · 2022
    Review

45 more citing papers are in PubMed but not listed here.

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

13 authors at 3 institutions in 1 country.

Eliza Li Shan FongDepartment of Bioengineering, Rice University, Houston, TX 77005, USA.
Salah-Eddine Lamhamedi-Cherradi
Emily Burdett
Vandhana Ramamoorthy
Alexander J Lazar
F Kurtis Kasper
Mary C Farach-Carson
Deeksha Vishwamitra
Elizabeth G Demicco
Brian A Menegaz
Hesham M Amin
Antonios G Mikos
Joseph A Ludwig
Rice University · USThe University of Texas MD Anderson Cancer Center · USMount Sinai Hospital · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Role of IGF-IR tyrosine kinase in NPM-ALK-expressing T-cell lymphomaR01CA151533 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI AMIN, HESHAM M · 2011 to 2015
$1.6M
Flow Perfusion Bioreactor Fabrication of Bioactive Polymer/ECM Hybrid ConstructsR01AR057083 · NIAMS · RICE UNIVERSITY · PI MIKOS, ANTONIOS G. · 2009 to 2013
$1.6M
NCI NIH HHS CA016672NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA151533NIAMS NIH HHS R01 AR057083
6 · The paper itself

Abstract

The pronounced biological influence of the tumor microenvironment on cancer progression and metastasis has gained increased recognition over the past decade, yet most preclinical antineoplastic drug testing is still reliant on conventional 2D cell culture systems. Although monolayer cultures recapitulate some of the phenotypic traits observed clinically, they are limited in their ability to model the full range of microenvironmental cues, such as ones elicited by 3D cell-cell and cell-extracellular matrix interactions. To address these shortcomings, we established an ex vivo 3D Ewing sarcoma model that closely mimics the morphology, growth kinetics, and protein expression profile of human tumors. We observed that Ewing sarcoma cells cultured in porous 3D electrospun poly(ε-caprolactone) scaffolds not only were more resistant to traditional cytotoxic drugs than were cells in 2D monolayer culture but also exhibited remarkable differences in the expression pattern of the insulin-like growth factor-1 receptor/mammalian target of rapamycin pathway. This 3D model of the bone microenvironment may have broad applicability for mechanistic studies of bone sarcomas and exhibits the potential to augment preclinical evaluation of antineoplastic drug candidates for these malignancies.

Indexed as

Tissue ScaffoldsAnimalsBlotting, WesternBone NeoplasmsCaproatesCell Line, TumorComputational BiologyFlow CytometryHumansImmunohistochemistryLactonesMiceMice, KnockoutMice, SCIDMicroscopy, Electron, ScanningReceptors, SomatomedinCaproatescaprolactoneLactonesReceptors, Somatomedin

Identifiers

PMID23576741
PMCPMC3631678
OpenAlexW2037221338

What OpenQuestion holds

Textmetadata
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.