ArticleIET systems biology
Deciphering the Molecular Mechanisms of Polycystic Ovary Syndrome and Flaxseed Therapy Through Transcriptomics and Machine Learning.
Article in IET systems biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- Artificial intelligence and machine learning in immunosenescence: from biomarker discovery to clinical translation.Frontiers in aging · 2026Review
- Deciphering the Molecular Mechanisms of Polycystic Ovary Syndrome and Flaxseed Therapy Through Transcriptomics and Machine Learning.IET systems biologyArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
Polycystic ovary syndrome (PCOS) is a prevalent endocrine and metabolic disorder characterised by heterogeneous clinical and molecular phenotypes. Flaxseed, widely used in traditional Chinese medicine and as a nutritional supplement, has shown promising therapeutic potential for PCOS. In this study, we integrated transcriptomic data with machine learning-based analytical approaches and network pharmacology to investigate the molecular mechanisms underlying PCOS and to identify the potential targets and pathways modulated by flaxseed. Differentially expressed genes (DEGs) and PCOS-related targets were systematically identified from GEO, GeneCards and DisGeNet databases. Bioactive compounds in flaxseed were predicted using TCMSP, SwissTargetPrediction and INPUT2.0. Functional and pathway enrichment analyses were conducted to explore mechanistic insights. Core targets were prioritised using Centiscape network topology parameters and LASSO regression, followed by molecular docking validation using AutoDock. Our results revealed that flaxseed's therapeutic action may primarily involve modulation of immune regulation, insulin signalling, apoptosis and inflammation pathways. Key active compounds, notably β-sitosterol and stigmasterol, exhibited strong binding affinities with critical targets, such as IL1B, GSK3B and HMGCR, suggesting potential anti-inflammatory and antioxidant effects. The findings provide a theoretical foundation for future experimental studies and support the development of flaxseed-based therapeutic strategies for PCOS through precision medicine frameworks.
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What Socratic holds
Registered trials
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.