Evidence map›Paper›PMID 40161596›Full record

ArticlebioRxiv : the preprint server for biology2025

Methods for Processing and Analyzing Images of Vascularized Micro-Organ and Tumor Systems.

Stephanie J Hachey, Christopher J Hatch, Daniela Gaebler, Alexander G Forsythe, Makena L Ewald, Alexander L Chopra, Jennifer S Fang, Christopher C W Hughes

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

5 · Who and what money

Authors and funding

8 authors.

Stephanie J HacheyUniversity of California, Irvine, Molecular Biology and Biochemistry, Irvine, CA, USA.
Christopher J HatchUniversity of California, Irvine, Biomedical Engineering, Irvine, CA, USA.
Daniela GaeblerUniversity of California, Irvine, Molecular Biology and Biochemistry, Irvine, CA, USA.
Alexander G ForsytheSimon Fraser University, Burnaby, British Columbia, Canada.ORCID 0000-0002-5185-0705
Makena L EwaldUniversity of California, Irvine, Molecular Biology and Biochemistry, Irvine, CA, USA.
Alexander L ChopraUniversity of California, Irvine, Molecular Biology and Biochemistry, Irvine, CA, USA.
Jennifer S FangTulane University, Cell and Molecular Biology, New Orleans, LA, USA.
Christopher C W HughesUniversity of California, Irvine, Molecular Biology and Biochemistry, Irvine, CA, USA.

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
Shared Resource Core: Single Cell AnalysisU54CA217378 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI LANDER, ARTHUR D · 2018 to 2022
$9.7M
NRSA Training CoreTL1TR001415 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI CAIOZZO, VINCENT JAMES, HEAD, ELIZABETH · 2015 to 2023
$4.2M
Identifying Therapeutic Targets for Stage III MelanomaR01CA244571 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI GANESAN, ANAND K · 2020 to 2024
$2.4M
A Vascularized Micro-Organ platform for the study of Brain-BBB-Blood interactionR33HL154307 · NHLBI · UNIVERSITY OF CALIFORNIA-IRVINE · PI HUGHES, CHRISTOPHER C. W., THOMPSON, LESLIE MICHELS · 2022 to 2024
$1.9M
Molecular basis for defective pericyte-endothelial cell interactions regulating vascular malformationsR01HL149748 · NHLBI · UNIVERSITY OF SOUTH FLORIDA · PI DAVIS, GEORGE E · 2020 to 2023
$1.5M
A Vascularized Micro-Organ platform for the study of Brain-BBB-Blood interactionR61HL154307 · NHLBI · UNIVERSITY OF CALIFORNIA-IRVINE · PI HUGHES, CHRISTOPHER C. W., THOMPSON, LESLIE MICHELS · 2020 to 2021
$1.3M
NCATS NIH HHS TL1 TR001415NCI NIH HHS P30 CA062203NCI NIH HHS R01 CA244571NCI NIH HHS U54 CA217378NHLBI NIH HHS R01 HL149748NHLBI NIH HHS R33 HL154307NHLBI NIH HHS R61 HL154307
6 · The paper itself

Abstract

Our group has developed and validated an advanced microfluidic platform to improve preclinical modeling of healthy and disease states, enabling extended culture and detailed analysis of tissue-engineered miniaturized organ constructs, or "organs-on-chips." Within this system, diverse cell types self-organize into perfused microvascular networks under dynamic flow within tissue chambers, effectively mimicking the structure and function of native tissues. This setup facilitates physiological intravascular delivery of nutrients, immune cells, and therapeutic agents, and creates a realistic microenvironment to study cellular interactions and tissue responses. Known as the vascularized micro-organ (VMO), this adaptable platform can be customized to represent various organ systems or tumors, forming a vascularized micro-tumor (VMT) for cancer studies. The VMO/VMT system closely simulates in vivo nutrient exchange and drug delivery within a 3D microenvironment, establishing a high-fidelity model for drug screening and mechanistic studies in vascular biology, cancer, and organ-specific pathologies. Furthermore, the optical transparency of the device supports high-resolution, real-time imaging of fluorescently labeled cells and molecules within the tissue construct, providing key insights into drug responses, cell interactions, and dynamic processes such as epithelial-mesenchymal transition. To manage the extensive imaging data generated, we created standardized, high-throughput workflows for image analysis. This manuscript presents our image processing and analysis pipeline, utilizing a suite of tools in Fiji/ImageJ to streamline data extraction from the VMO/VMT model, substantially reducing manual processing time. Additionally, we demonstrate how these tools can be adapted for analyzing imaging data from traditional

Indexed as

bioengineeringimage processingmicrofluidicmicrophysiological systemtherapeutic developmenttumor microenvironmenttumor on chip

Identifiers

PMID40161596
PMCPMC11952417

What OpenQuestion holds

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LicenceCC BY-NC
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.