Evidence map›Paper›PMID 26365200›Full record

ArticleScientific reports2015

A spheroid toxicity assay using magnetic 3D bioprinting and real-time mobile device-based imaging.

Hubert Tseng, Jacob A Gage, Tsaiwei Shen, William L Haisler, Shane K Neeley, Sue Shiao, Jianbo Chen, Pujan K Desai, Angela Liao, Chris Hebel and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

65 citing papers in PubMed, 145 citations in OpenAlex.

  1. Review
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  3. Article
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  8. Review
  9. Article
  10. Article
  11. Bioprinted research models of urological malignancy.Exploration (Beijing, China) · 2024
    Review
  12. Review
  13. The Antiproliferative Effect of Chloroform Fraction ofPharmaceuticals (Basel, Switzerland) · 2023
    Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Three-dimensional models: a novel approach for lymphoma research.Journal of cancer research and clinical oncology · 2022
    Review
  20. Article

5 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 2 institutions in 1 country.

Hubert TsengNano3D Biosciences (n3D), Houston, TX 77030 USA.
Jacob A GageNano3D Biosciences (n3D), Houston, TX 77030 USA.
Tsaiwei ShenLC Sciences, Houston, TX 77054 USA.
William L HaislerNano3D Biosciences (n3D), Houston, TX 77030 USA.
Shane K NeeleyNano3D Biosciences (n3D), Houston, TX 77030 USA.
Sue ShiaoNano3D Biosciences (n3D), Houston, TX 77030 USA.
Jianbo ChenDepartment of Physics, Rice University, Houston, TX 77005 USA.
Pujan K DesaiNano3D Biosciences (n3D), Houston, TX 77030 USA.
Angela LiaoNano3D Biosciences (n3D), Houston, TX 77030 USA.
Chris HebelLC Sciences, Houston, TX 77054 USA.
Robert M RaphaelDepartment of Bioengineering, Rice University, Houston, TX 77005 USA.
Jeanne L BeckerNano3D Biosciences (n3D), Houston, TX 77030 USA.
Glauco R SouzaNano3D Biosciences (n3D), Houston, TX 77030 USA.
Nano3D Biosciences (United States) · USRice University · US

Funding

Novel 3D high-content/throughput assay with mobile device-based data acquisitionR43ES024644 · NIEHS · NANO3D BIOSCIENCES, INC. · PI SOUZA, GLAUCO RANNA, TSENG, HUBERT · 2014 to 2014
$150k
NIEHS NIH HHS R43 ES024644NIEHS NIH HHS R43ES024644
6 · The paper itself

Abstract

An ongoing challenge in biomedical research is the search for simple, yet robust assays using 3D cell cultures for toxicity screening. This study addresses that challenge with a novel spheroid assay, wherein spheroids, formed by magnetic 3D bioprinting, contract immediately as cells rearrange and compact the spheroid in relation to viability and cytoskeletal organization. Thus, spheroid size can be used as a simple metric for toxicity. The goal of this study was to validate spheroid contraction as a cytotoxic endpoint using 3T3 fibroblasts in response to 5 toxic compounds (all-trans retinoic acid, dexamethasone, doxorubicin, 5'-fluorouracil, forskolin), sodium dodecyl sulfate (+control), and penicillin-G (-control). Real-time imaging was performed with a mobile device to increase throughput and efficiency. All compounds but penicillin-G significantly slowed contraction in a dose-dependent manner (Z' = 0.88). Cells in 3D were more resistant to toxicity than cells in 2D, whose toxicity was measured by the MTT assay. Fluorescent staining and gene expression profiling of spheroids confirmed these findings. The results of this study validate spheroid contraction within this assay as an easy, biologically relevant endpoint for high-throughput compound screening in representative 3D environments.

Indexed as

3T3 CellsAnimalsAnti-Bacterial AgentsAntineoplastic AgentsCell Culture TechniquesHigh-Throughput Screening AssaysMagneticsMiceMicroscopy, FluorescencePenicillin GSodium Dodecyl SulfateSpheroids, CellularTranscriptomeAnti-Bacterial AgentsAntineoplastic AgentsPenicillin GSodium Dodecyl Sulfate

Identifiers

PMID26365200
PMCPMC4568483
OpenAlexW2411123878

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.