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<article xsi:noNamespaceSchemaLocation="http://jats.nlm.nih.gov/publishing/1.1/xsd/JATS-journalpublishing1-mathml3.xsd" dtd-version="1.1" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><front><journal-meta><journal-id journal-id-type="publisher-id">JCNR</journal-id><journal-title-group><journal-title>Journal of Clinical and Nursing Research</journal-title></journal-title-group><issn>2208-3685</issn><eissn>2208-3693</eissn><publisher><publisher-name>Bio-Byword Scientific Publishing Pty. Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.26689/jcnr.v10i6.15537</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title>Network Pharmacological and Molecular Mechanism Analysis of Bovine Embryonic Stem Cell Telomere-Mitochondria Polypeptides (EST-Mips) in Anti-Aging</title><url>https://artdesignp.com/journal/JCNR/10/6/10.26689/jcnr.v10i6.15537</url><author>HaoJunjie,DingPengcheng,JiangHuoqiang,ZhangJiren</author><pub-date pub-type="publication-year"><year>2026</year></pub-date><volume>10</volume><issue>6</issue><history><date date-type="pub"><published-time>2026-06-30</published-time></date></history><abstract>Embryonic stem cell telomere-mitochondrial peptides (EST-Mips) are a group of peptide molecules derived from bovine embryonic stem cells, closely associated with telomere maintenance and mitochondrial function. In this study, based on 736 EST-Mips-regulated protein targets provided by users, we employed network pharmacology and bioinformatics approaches to systematically elucidate their molecular mechanisms in delaying the aging process. By screening target-aging associations using platforms such as PubChem, GeneCards, Human Aging Genomic Resources (HAGR/GenAge), Open Genes, and AgeAnno, we identified a total of 179 shared aging-related targets (accounting for 24.3% of all targets). Key targets include hub proteins with node connectivity ≥ 50, such as TP53, AKT1, SRC, EGFR, TNF, IL6, MAPK1, and MAPK3. GO functional enrichment analysis revealed that EST-Mips primarily participate in cell cycle regulation, apoptosis signaling, oxidative stress response, and inflammatory responses. KEGG pathway analysis demonstrated that EST-Mips exert their anti-aging effects by modulating aging-related signaling pathways, including PI3K-Akt, FoxO, p53, MAPK, JAK-STAT, and NF-κB. 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