Evidence map›Paper›PMID 40746721›Full record

ArticleFrontiers in pharmacology2025

Machine learning-enhanced discovery of tsRNA-mRNA regulatory networks: identifying novel diagnostic biomarkers and therapeutic targets in breast cancer.

Zhongling Ma, Rui Wang, Ming Yuan, Bo Wang, Li Li, Tianfu Zhao, Xinhan Zhao

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Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Zhongling Ma *Department of Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Rui Wang *Department of Thoracic Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Ming YuanDepartment of Oncology, Xi'an Chang'an District Hospital, Xi'an, Shaanxi, China.
Bo WangDepartment of Oncology, Xi'an Chang'an District Hospital, Xi'an, Shaanxi, China.
Li LiDepartment of Oncology, Xi'an Chang'an District Hospital, Xi'an, Shaanxi, China.
Tianfu ZhaoDepartment of Oncology, Xi'an Chang'an District Hospital, Xi'an, Shaanxi, China.
Xinhan ZhaoDepartment of Oncology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Transfer RNA-derived small RNAs (tsRNAs) represent an emerging class of regulatory molecules with potential as cancer biomarkers. However, their diagnostic utility and regulatory mechanisms in breast cancer remain poorly characterized. This study integrates machine learning algorithms with traditional molecular biology approaches to identify tsRNA-based diagnostic signatures and their downstream targets. Methods: We analyzed miRNA-seq data from 103 matched tumor-normal pairs from TCGA-BRCA as the discovery cohort and GSE117452 as validation. tsRNA profiles were extracted using a custom bioinformatics pipeline. Random forest algorithm was employed to develop a diagnostic model. Correlation analysis and RNAhybrid were used to identify tsRNA-mRNA regulatory relationships. Comprehensive multi-omics analyses including survival, immune infiltration, drug sensitivity, and pathway enrichment were performed for identified targets. Functional validation was conducted in breast cancer cell lines. Results: We identified 297 differentially expressed tsRNAs and developed a four-tsRNA signature (tRF-21-FSXMSL73E, tRF-20-XSXMSL73, tRF-23-FSXMSL730H, tRF-23-YJE76INB0J) achieving AUC of 0.98 in discovery and 0.82 in validation cohorts. tRF-21-FSXMSL73E showed strong correlation with FAM155B expression. Pan-cancer analysis revealed FAM155B overexpression in multiple malignancies with prognostic significance. FAM155B correlated with immune infiltration, drug resistance, and activation of oncogenic pathways. Functional studies confirmed FAM155B promotes breast cancer proliferation and migration. Conclusion: Our machine learning approach successfully identified a robust tsRNA diagnostic signature and uncovered the tsRNA-FAM155B regulatory axis as a novel therapeutic target. This integrated methodology provides a framework for accelerating biomarker discovery by combining computational prediction with traditional validation, advancing precision medicine in breast cancer.

Indexed as

biomarker discoverybreast cancerFAM155Bmachine learningtsRNA

Identifiers

PMID40746721
PMCPMC12310640

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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.