Evidence map›Paper›PMID 31639124›Full record

ArticlePloS one2019

Structure establishment of three-dimensional (3D) cell culture printing model for bladder cancer.

Myeong Joo Kim, Byung Hoon Chi, James J Yoo, Young Min Ju, Young Mi Whang, In Ho Chang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

38 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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  5. Article
  6. Review
  7. Review
  8. Bioprinted research models of urological malignancy.Exploration (Beijing, China) · 2024
    Review
  9. Article
  10. Review
  11. Review
  12. Article
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  14. Review
  15. Article
  16. Review
  17. 3D Tumor Models in Urology.International journal of molecular sciences · 2023
    Review
  18. Review
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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

6 authors at 2 institutions in 2 countries.

Myeong Joo KimDepartment of Urology, College of Medicine, Chung-Ang University, Seoul, Republic of Korea.
Byung Hoon ChiDepartment of Urology, College of Medicine, Chung-Ang University, Seoul, Republic of Korea.
James J YooWake Forest Institute for Regenerative Medicine, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, United States of America.
Young Min JuWake Forest Institute for Regenerative Medicine, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC, United States of America.
Young Mi WhangDepartment of Urology, College of Medicine, Chung-Ang University, Seoul, Republic of Korea.
In Ho ChangDepartment of Urology, College of Medicine, Chung-Ang University, Seoul, Republic of Korea.ORCID 0000-0003-0240-1310
Chung-Ang University · KRForest Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTwo-dimensional (2D) cell culture is a valuable method for cell-based research but can provide unpredictable, misleading data about in vivo responses. In this study, we created a three-dimensional (3D) cell culture environment to mimic tumor characteristics and cell-cell interactions to better characterize the tumor formation response to chemotherapy. MATERIALS AND

methodsWe fabricated the 3D cell culture samples using a 3D cell bio printer and the bladder cancer cell line 5637. T24 cells were used for 2D cell culture. Then, rapamycin and Bacillus Calmette-Guérin (BCG) were used to examine their cancer inhibition effects using the two bladder cancer cell lines. Cell-cell interaction was measured by measuring e-cadherin and n-cadherin secreted via the epithelial-mesenchymal transition (EMT).

resultsWe constructed a 3D cell scaffold using gelatin methacryloyl (GelMA) and compared cell survival in 3D and 2D cell cultures. 3D cell cultures showed higher cancer cell proliferation rates than 2D cell cultures, and the 3D cell culture environment showed higher cell-to-cell interactions through the secretion of E-cadherin and N-cadherin. Assessment of the effects of drugs for bladder cancer such as rapamycin and BCG showed that the effect in the 2D cell culture environment was more exaggerated than that in the 3D cell culture environment.

conclusionsWe fabricated 3D scaffolds with bladder cancer cells using a 3D bio printer, and the 3D scaffolds were similar to bladder cancer tissue. This technique can be used to create a cancer cell-like environment for a drug screening platform.

Indexed as

Cell Culture TechniquesPrinting, Three-DimensionalSpheroids, CellularTumor Cells, CulturedCell CommunicationCell Line, TumorCell ProliferationCell SurvivalCytokinesHumansUrinary Bladder NeoplasmsCytokines

Identifiers

PMID31639124
PMCPMC6804961
OpenAlexW2981735527

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.