Evidence map›Paper›PMID 37795818›Full record

ArticleJournal of cell science2023

'Chip'-ing away at morphogenesis - application of organ-on-chip technologies to study tissue morphogenesis.

Matthew J White, Tania Singh, Eric Wang, Quinton Smith, Matthew L Kutys

Abstract read
In one paragraph

Article in Journal of cell science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Matthew J WhiteDepartment of Cell and Tissue Biology, University of California San Francisco, San Francisco, CA 94143, USA.
Tania SinghDepartment of Cell and Tissue Biology, University of California San Francisco, San Francisco, CA 94143, USA.
Eric WangDepartment of Chemical and Biomolecular Engineering, University of California Irvine, Irvine, CA 92697, USA.ORCID 0000-0001-9903-2640
Quinton SmithDepartment of Chemical and Biomolecular Engineering, University of California Irvine, Irvine, CA 92697, USA.ORCID 0000-0001-7079-1176
Matthew L KutysDepartment of Cell and Tissue Biology, University of California San Francisco, San Francisco, CA 94143, USA.ORCID 0000-0002-0752-649X

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
Physicochemical control of multilineage emergenceR35GM151099 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI Quinton Smith · 2023 to 2026
$1.5M
Decoding cortical Notch signaling and morphogenic instruction at cell-cell interfacesR35GM150987 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KUTYS, MATTHEW L · 2023 to 2025
$1.3M
Non-canonical Notch1 regulation of proliferation and adherens junctions in breast cancerR00CA226366 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KUTYS, MATTHEW L · 2020 to 2022
$667k
Notch1 and APP signaling in cerebral microvascular dysfunctionR21AG072232 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JUN, YOUNG-WOOK, KUTYS, MATTHEW L · 2021 to 2021
$439k
Non-canonical Notch1 regulation of proliferation and adherens junctions in breast cancerK99CA226366 · NCI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI KUTYS, MATTHEW L · 2018 to 2019
$323k
Howard Hughes Medical InstituteNCI NIH HHS K99 CA226366NCI NIH HHS P30 CA062203NCI NIH HHS R00 CA226366NIA NIH HHS R21 AG072232NIGMS NIH HHS R35 GM150987NIGMS NIH HHS R35 GM151099
6 · The paper itself

Abstract

Emergent cell behaviors that drive tissue morphogenesis are the integrated product of instructions from gene regulatory networks, mechanics and signals from the local tissue microenvironment. How these discrete inputs intersect to coordinate diverse morphogenic events is a critical area of interest. Organ-on-chip technology has revolutionized the ability to construct and manipulate miniaturized human tissues with organotypic three-dimensional architectures in vitro. Applications of organ-on-chip platforms have increasingly transitioned from proof-of-concept tissue engineering to discovery biology, furthering our understanding of molecular and mechanical mechanisms that operate across biological scales to orchestrate tissue morphogenesis. Here, we provide the biological framework to harness organ-on-chip systems to study tissue morphogenesis, and we highlight recent examples where organ-on-chips and associated microphysiological systems have enabled new mechanistic insight in diverse morphogenic settings. We further highlight the use of organ-on-chip platforms as emerging test beds for cell and developmental biology.

Indexed as

Microphysiological SystemsTissue EngineeringHumansMorphogenesisCell and developmental biologyMicrophysiological systemsOrganoidsOrgan-on-chipTissue morphogenesis

Identifiers

PMID37795818
PMCPMC10565497

What Socratic 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 Socratic graph.