Evidence map›Paper›PMID 36251352›Full record

ArticleJournal of surgical oncology2023

Deep learning image analysis quantifies tumor heterogeneity and identifies microsatellite instability in colon cancer.

Jill C Rubinstein, Ali Foroughi Pour, Jie Zhou, Todd B Sheridan, Brian S White, Jeffrey H Chuang

Abstract read
In one paragraph

Article in Journal of surgical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
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  7. Deep Learning Image Processing Models in Dermatopathology.Diagnostics (Basel, Switzerland) · 2025
    Review
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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

6 authors.

Jill C RubinsteinThe Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.ORCID http://orcid.org/0000-0002-1222-8657
Ali Foroughi PourThe Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.
Jie ZhouThe Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.
Todd B SheridanThe Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.
Brian S WhiteThe Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.
Jeffrey H ChuangThe Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.

Funding

Quantitative Computational Methods to Accurately Measure Tumor Heterogeneity in Solid Tumors to Inform Development of Evolution-based Treatment StrategiesR01CA230031 · NCI · JACKSON LABORATORY · PI CHUANG, JEFFREY HSU-MIN · 2018 to 2022
$2.6M
NCI NIH HHS R01 CA230031
6 · The paper itself

Abstract

BACKGROUND AND

objectivesDeep learning utilizing convolutional neural networks (CNNs) applied to hematoxylin & eosin (H&E)-stained slides numerically encodes histomorphological tumor features. Tumor heterogeneity is an emerging biomarker in colon cancer that is, captured by these features, whereas microsatellite instability (MSI) is an established biomarker traditionally assessed by immunohistochemistry or polymerase chain reaction.

methodsH&E-stained slides from The Cancer Genome Atlas (TCGA) colon cohort are passed through the CNN. Resulting imaging features are used to cluster morphologically similar slide regions. Tile-level pairwise similarities are calculated and used to generate a tumor heterogeneity score (THS). Patient-level THS is then correlated with TCGA-reported biomarkers, including MSI-status.

resultsH&E-stained images from 313 patients generated 534 771 tiles. Deep learning automatically identified and annotated cells by type and clustered morphologically similar slide regions. MSI-high tumors demonstrated significantly higher THS than MSS/MSI-low (p < 0.001). THS was higher in MLH1-silent versus non-silent tumors (p < 0.001). The sequencing derived MSIsensor score also correlated with THS (r = 0.51, p < 0.0001).

conclusionsDeep learning provides spatially resolved visualization of imaging-derived biomarkers and automated quantification of tumor heterogeneity. Our novel THS correlates with MSI-status, indicating that with expanded training sets, translational tools could be developed that predict MSI-status using H&E-stained images alone.

Indexed as

Colonic NeoplasmsColorectal NeoplasmsDeep LearningHumansMicrosatellite InstabilityMicrosatellite Repeatscolon cancerdeep learningmicrosatellite instabilitytumor heterogeneity

Identifiers

PMID36251352
PMCPMC11446314

What OpenQuestion holds

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Registered trials

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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.