Evidence map›Paper›PMID 38780888›Full record

ArticleBreast cancer research and treatment2024

Pathomic model based on histopathological features and machine learning to predict IDO1 status and its association with breast cancer prognosis.

Xiaohua Zhuo, Hailong Deng, Mingzhu Qiu, Xiaoming Qiu

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Article in Breast cancer research and treatment, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xiaohua Zhuo *Department of Pathology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, Fujian, China.
Hailong Deng *Department of Pathology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, Fujian, China.
Mingzhu QiuDepartment of Pathology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, Fujian, China.
Xiaoming QiuDepartment of Pathology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, Fujian, China. fjqiuxiaoming@163.com.

Funding

Longyan City Science and Technology Plan Project 2022LYF17023
6 · The paper itself

Abstract

purposeTo establish a pathomic model using histopathological image features for predicting indoleamine 2,3-dioxygenase 1 (IDO1) status and its relationship with overall survival (OS) in breast cancer.

methodsA pathomic model was constructed using machine learning and histopathological images obtained from The Cancer Genome Atlas database to predict IDO1 expression. The model performance was evaluated based on the area under the curve, calibration curve, and decision curve analysis (DCA). Prediction scores (PSes) were generated from the model and applied to divide the patients into two groups. Survival outcomes, gene set enrichment, immune microenvironment, and tumor mutations were assessed between the two groups.

resultsSurvival analysis followed by multivariate correction revealed that high IDO1 is a protective factor for OS. Further, the model was calibrated, and it exhibited good discrimination. Additionally, the DCA showed that the proposed model provided a good clinical net benefit. The Kaplan-Meier analysis revealed a positive correlation between high PS and improved OS. Univariate and multivariate Cox regression analyses demonstrated that PS is an independent protective factor for OS. Moreover, differentially expressed genes were enriched in various essential biological processes, including extracellular matrix receptor interaction, angiogenesis, transforming growth factor β signaling, epithelial mesenchymal transition, cell junction, tryptophan metabolism, and heme metabolic processes. PS was positively correlated with M1 macrophages, CD8 + T cells, T follicular helper cells, and tumor mutational burden.

conclusionThese results indicate the potential ability of the proposed pathomic model to predict IDO1 status and the OS of breast cancer patients.

Indexed as

Biomarkers, TumorBreast NeoplasmsIndoleamine-Pyrrole 2,3,-DioxygenaseMachine LearningTumor MicroenvironmentFemaleGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateMiddle AgedPrognosisBiomarkers, TumorIDO1 protein, humanIndoleamine-Pyrrole 2,3,-DioxygenaseBreast cancerHistopathological featureIDO1ImmunotherapyPathomic modelPrognosis

Identifiers

PMID38780888
PMCPMC11230954

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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.