Evidence map›Paper›PMID 30366681›Full record

ReviewKidney international2018

Kidney-on-a-chip: untapped opportunities.

Nureddin Ashammakhi, Katherine Wesseling-Perry, Anwarul Hasan, Elmahdi Elkhammas, Yu Shrike Zhang

Open access · bronzeAbstract readReview
In one paragraph

Review in Kidney international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

79 citing papers in PubMed, 163 citations in OpenAlex.

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19 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

5 authors at 5 institutions in 4 countries.

Nureddin AshammakhiDivision of Plastic Surgery, Department of Surgery, Oulu University Hospital, Oulu, Finland; Biotechnology Research Center, Libyan Authority for Research, Science and Technology, Tripoli, Libya. Electronic address: nureddin.ashammakhi@oulu.fi.
Katherine Wesseling-PerryDivision of Nephrology, Department of Pediatrics, David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
Anwarul HasanDepartment of Mechanical and Industrial Engineering, College of Engineering, Qatar University, Doha, Qatar. Electronic address: ahasan@qu.edu.qa.
Elmahdi ElkhammasDivision of Transplantation Surgery, Department of Surgery, The Ohio State University Wexner Medical Center, Comprehensive Transplant Center, Columbus, Ohio, USA.
Yu Shrike ZhangDivision of Engineering in Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Cambridge, Massachusetts, USA.
Harvard University · USOulu University Hospital · FIQatar University · QAThe Ohio State University Wexner Medical Center · USUniversity of California, Los Angeles · US

Funding

Multiscale Stereolithogrphic Bioprinting of Stage-Matching Vascularized Tumor ModelsR21EB025270 · NIBIB · BRIGHAM AND WOMEN'S HOSPITAL · PI ZHANG, Y. SHRIKE · 2018 to 2020
$726k
Recapitulating Ductal Carcinoma on a Chip for Personalized Breast Cancer TherapyK99CA201603 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI ZHANG, Y. SHRIKE · 2016 to 2017
$356k
NCI NIH HHS K99 CA201603NIBIB NIH HHS R21 EB025270
6 · The paper itself

Abstract

The organs-on-a-chip technology has shown strong promise in mimicking the complexity of native tissues in vitro and ex vivo, and recently significant advances have been made in applying this technology to studies of the kidney and its diseases. Individual components of the nephron, including the glomerulus, proximal tubule, and distal tubule/medullary collecting duct, have been successfully mimicked using organs-on-a-chip technology and yielding strong promises in advancing the field of ex vivo drug toxicity testing and augmenting renal replacement therapies. Although these models show promise over 2-dimensional cell systems in recapitulating important nephron features in vitro, nephron functions, such as tubular secretion, intracellular metabolism, and renin and vitamin D production, as well as prostaglandin synthesis are still poorly recapitulated in on-chip models. Moreover, construction of multiple-renal-components-on-a-chip models, in which various structures and cells of the renal system interact with each other, has remained a challenge. Overall, on-chip models show promise in advancing models of normal and pathological renal physiology, in predicting nephrotoxicity, and in advancing treatment of chronic kidney diseases.

Indexed as

BioreactorsLab-On-A-Chip DevicesMicrochip Analytical ProceduresRenal Replacement TherapyAnimalsDrug DevelopmentEquipment DesignHumansKidneyKidney DiseasesToxicity Testskidneymicrofluidicsmicrophysiological systemsorgan-on-a-chiptissue engineering

Identifiers

PMID30366681
PMCPMC6408139
OpenAlexW2897146184

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.