Evidence map›Paper›PMID 30291268›Full record

ArticleScientific reports2018

Technology Transfer of the Microphysiological Systems: A Case Study of the Human Proximal Tubule Tissue Chip.

Courtney Sakolish, Elijah J Weber, Edward J Kelly, Jonathan Himmelfarb, Roula Mouneimne, Fabian A Grimm, John S House, Terry Wade, Arum Han, Weihsueh A Chiu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. 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
4.7field-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, 77 citations in OpenAlex.

  1. Review
  2. Beyond monolayers: a comparative analysis of 2D cell cultures and 3DFrontiers in bioengineering and biotechnology · 2026
    Review
  3. Review
  4. Article
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  9. Review
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  11. Article
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  14. Multivariate Pharma Technology Transfer Analysis: Civilization Diseases and COVID-19 Perspective.International journal of environmental research and public health · 2023
    Article
  15. Review
  16. Microphysiological Systems Evaluation: Experience of TEX-VAL Tissue Chip Testing Consortium.Toxicological sciences : an official journal of the Society of Toxicology · 2022
    Article
  17. Review
  18. Emerging technologies and their impact on regulatory science.Experimental biology and medicine (Maywood, N.J.) · 2022
    Review
  19. Review
  20. Review
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

11 authors at 3 institutions in 1 country.

Courtney SakolishDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX, USA.
Elijah J WeberDepartment of Pharmaceutics, University of Washington, Seattle, WA, USA.
Edward J KellyDepartment of Pharmaceutics, University of Washington, Seattle, WA, USA.
Jonathan HimmelfarbDivision of Nephrology, University of Washington Kidney Research Institute, Seattle, WA, USA.
Roula MouneimneDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX, USA.
Fabian A GrimmDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX, USA.
John S HouseBioinformatics Research Center, North Carolina State University, Raleigh, NC, USA.ORCID http://orcid.org/0000-0002-8447-7871
Terry WadeGeochemical and Environmental Research Group, Texas A&M University, College Station, TX, USA.
Arum HanDepartment of Electrical and Computer Engineering, Texas A&M University, College Station, TX, USA.
Weihsueh A ChiuDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX, USA.
Ivan RusynDepartment of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX, USA. irusyn@tamu.edu.
Texas A&M University · USUniversity of Washington · USNorth Carolina State University · US

Funding

XENOBIOTIC BIOTRANSFORMATION AND DISPOSITIONP30ES007033 · NIEHS · UNIVERSITY OF WASHINGTON · PI ALI SHOJAIE · 1995 to 2026
$42.5M
Using iPSCs to model patient outcomes in nephrotic syndromeUH3TR000504 · NCATS · UNIVERSITY OF WASHINGTON · PI HIMMELFARB, JONATHAN · 2014 to 2016
$6.1M
TEX-VAL: Texas A&M Tissue Chip Validation CenterU24TR001950 · NCATS · TEXAS A&M UNIVERSITY · PI RUSYN, IVAN · 2016 to 2017
$4.2M
Regulatory Science in Environmental Health and ToxicologyT32ES026568 · NIEHS · TEXAS A&M UNIVERSITY · PI Weihsueh A Chiu, Natalie M Johnson · 2016 to 2026
$3.8M
A Tissue Engineered Human Kidney Microphysiological SystemUH2TR000504 · NCATS · UNIVERSITY OF WASHINGTON · PI HIMMELFARB, JONATHAN · 2012 to 2013
$2.1M
NCATS NIH HHS U24 TR001950NCATS NIH HHS UH2 TR000504NCATS NIH HHS UH3 TR000504NIEHS NIH HHS P30 ES007033NIEHS NIH HHS T32 ES026568
6 · The paper itself

Abstract

The adoption of a new technology into basic research, and industrial and clinical settings requires rigorous testing to build confidence in the reproducibility, reliability, robustness, and relevance of these models. Tissue chips are promising new technology, they have the potential to serve as a valuable tool in biomedical research, as well as pharmaceutical development with regards to testing for efficacy and safety. The principal goals of this study were to validate a previously established proximal tubule tissue chip model in an independent laboratory and to extend its utility to testing of nephrotoxic compounds. Here, we evaluated critical endpoints from the tissue chip developer laboratory, focusing on biological relevance (long-term viability, baseline protein and gene expression, ammoniagenesis, and vitamin D metabolism), and toxicity biomarkers. Tissue chip experiments were conducted in parallel with traditional 2D culture conditions using two different renal proximal tubule epithelial cell sources. The results of these studies were then compared to the findings reported by the tissue chip developers. While the overall transferability of this advanced tissue chip platform was a success, the reproducibility with the original report was greatly dependent on the cell source. This study demonstrates critical importance of developing microphysiological platforms using renewable cell sources.

Indexed as

Lab-On-A-Chip DevicesAnti-Bacterial AgentsCell Culture TechniquesCell LineCell SurvivalDrug DevelopmentDrug Evaluation, PreclinicalHumansKidney Tubules, ProximalPolymyxin BTechnology TransferVitamin DAnti-Bacterial AgentsPolymyxin BVitamin D

Identifiers

PMID30291268
PMCPMC6173737
OpenAlexW2895351357

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.