Evidence map›Paper›PMID 39184400›Full record

ArticleJournal of biomedical optics2024

Utilizing convolutional neural networks for discriminating cancer and stromal cells in three-dimensional cell culture images with nuclei counterstain.

Huu Tuan Nguyen, Nicholas Pietraszek, Sarah E Shelton, Kwabena Arthur, Roger D Kamm

Abstract read
In one paragraph

Article in Journal of biomedical optics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Huu Tuan NguyenMassachusetts Institute of Technology (MIT), Department of Mechanical Engineering and Department of Biological Engineering, Cambridge, Massachusetts, United States.ORCID 0000-0001-6130-2828
Nicholas PietraszekMassachusetts Institute of Technology (MIT), Department of Mechanical Engineering and Department of Biological Engineering, Cambridge, Massachusetts, United States.
Sarah E SheltonMassachusetts Institute of Technology (MIT), Department of Mechanical Engineering and Department of Biological Engineering, Cambridge, Massachusetts, United States.ORCID 0000-0002-9358-058X
Kwabena ArthurMassachusetts Institute of Technology (MIT), Department of Mechanical Engineering and Department of Biological Engineering, Cambridge, Massachusetts, United States.
Roger D KammMassachusetts Institute of Technology (MIT), Department of Mechanical Engineering and Department of Biological Engineering, Cambridge, Massachusetts, United States.ORCID 0000-0002-7232-304X

Funding

The Center for Label-free Imagingand Multiscale Biophotonics (CLIMB)P41EB031772 · NIBIB · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI Stephen A Boppart · 2022 to 2026
$7.6M
Development of Physiologic Tissue Models to Assess Tumor Explant Response to Immune Checkpoint BlockadeU01CA214381 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BARBIE, DAVID A, KAMM, ROGER D · 2017 to 2021
$3.5M
Imaging Cancer Angiogenesis with Acoustic Angiography UltrasoundK00CA212227 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SHELTON, SARAH ELIZABETH · 2018 to 2021
$392k
NCI NIH HHS K00 CA212227NCI NIH HHS U01 CA214381NIBIB NIH HHS P41 EB031772
6 · The paper itself

Abstract

Significance: Accurate cell segmentation and classification in three-dimensional (3D) images are vital for studying live cell behavior and drug responses in 3D tissue culture. Evaluating diverse cell populations in 3D cell culture over time necessitates non-toxic staining methods, as specific fluorescent tags may not be suitable, and immunofluorescence staining can be cytotoxic for prolonged live cell cultures. Aim: We aim to perform machine learning-based cell classification within a live heterogeneous cell culture population grown in a 3D tissue culture relying only on reflectance, transmittance, and nuclei counterstained images obtained by confocal microscopy. Approach: In this study, we employed a supervised convolutional neural network (CNN) to classify tumor cells and fibroblasts within 3D-grown spheroids. These cells are first segmented using the marker-controlled watershed image processing method. Training data included nuclei counterstaining, reflectance, and transmitted light images, with stained fibroblast and tumor cells as ground-truth labels. Results: Our results demonstrate the successful marker-controlled watershed segmentation of 84% of spheroid cells into single cells. We achieved a median accuracy of 67% (95% confidence interval of the median is 65-71%) in identifying cell types. We also recapitulate the original 3D images using the CNN-classified cells to visualize the original 3D-stained image's cell distribution. Conclusion: This study introduces a non-invasive toxicity-free approach to 3D cell culture evaluation, combining machine learning with confocal microscopy, opening avenues for advanced cell studies.

Indexed as

Cell NucleusNeural Networks, ComputerStromal CellsCell Culture Techniques, Three DimensionalCell Line, TumorFibroblastsHumansImage Processing, Computer-AssistedImaging, Three-DimensionalMicroscopy, ConfocalNeoplasmsSpheroids, Cellularcell classificationconfocal microscopyconvolutional neural networksthree-dimensional cell culture

Identifiers

PMID39184400
PMCPMC11344342

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.