Evidence map›Paper›PMID 39684741›Full record

ArticleInternational journal of molecular sciences2024

Metabolomics-Based Machine Learning Models Accurately Predict Breast Cancer Estrogen Receptor Status.

Kamala K Arumalla, Jean-François Haince, Rashid A Bux, Guoyu Huang, Paramjit S Tappia, Bram Ramjiawan, W Randolph Ford, Maria Vaida

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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

8 authors.

Kamala K ArumallaDepartment of Analytics, Harrisburg University of Science and Technology, Harrisburg, PA 17101, USA.
Jean-François HainceBioMark Diagnostic Solutions Inc., Quebec, QC G1K 3G5, Canada.ORCID 0009-0002-5261-9967
Rashid A BuxBioMark Diagnostics Inc., Richmond, BC V6X 2W2, Canada.
Guoyu HuangBioMark Diagnostic Solutions Inc., Quebec, QC G1K 3G5, Canada.ORCID 0009-0004-5854-9482
Paramjit S TappiaAsper Clinical Research Institute, Winnipeg, MB R2H2A6, Canada.ORCID 0000-0001-8307-2760
Bram RamjiawanAsper Clinical Research Institute, Winnipeg, MB R2H2A6, Canada.
W Randolph FordDepartment of Analytics, Harrisburg University of Science and Technology, Harrisburg, PA 17101, USA.
Maria VaidaDepartment of Analytics, Harrisburg University of Science and Technology, Harrisburg, PA 17101, USA.

Funding

BioMark Diagnostics Inc (Richmond, BC, Canada) N/A
6 · The paper itself

Abstract

Breast cancer is a global concern as a leading cause of death for women. Early and precise diagnosis can be vital in handling the disease efficiently. Breast cancer subtyping based on estrogen receptor (ER) status is crucial for determining prognosis and treatment. This study uses metabolomics data from plasma samples to detect metabolite biomarkers that could distinguish ER-positive from ER-negative breast cancers in a non-invasive manner. The dataset includes demographic information, ER status, and metabolite levels from 188 breast cancer patients and 73 healthy controls. Recursive Feature Elimination (RFE) with a Random Forest (RF) classifier identified an optimal subset of 30 features-29 biomarkers and age-that achieved the highest area under the curve (AUC). To address the class imbalance, Gaussian noise-based augmentation and Adaptive Synthetic Oversampling (ADASYN) were applied, ensuring balanced representation during training. Four machine learning (ML) algorithms-Random Forest, Support Vector Classifier (SVC), XGBoost, and Logistic Regression (LR)-were evaluated using grid search. The Random Forest classifier emerged as the top performer, achieving an AUC of 0.95 and an accuracy of 93%. These results suggest that ML has great promise for identifying specific metabolites linked to ER expression, paving the development of a novel analytical tool that can minimize current challenges in identifying ER status, and improve the precision of breast cancer subtyping.

Indexed as

Biomarkers, TumorBreast NeoplasmsMachine LearningMetabolomicsReceptors, EstrogenAdultAgedAlgorithmsFemaleHumansMiddle AgedSupport Vector MachineBiomarkers, TumorReceptors, Estrogenbreast cancerestrogen receptorsmachine learning modelsmetabolomics

Identifiers

PMID39684741
PMCPMC11641454

What Socratic 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 Socratic graph.