Authors
Siyun Peng, Hangyu Wang, Ermao Li
Published in
Epigenetics. Volume 21. Issue 1. Pages 2758456. Epub Nov 09, 2026.
Abstract
PIWI-interacting RNAs (piRNAs) are small non-coding RNAs generated from longer precursor transcripts through primary processing and, in selected biological contexts, a secondary ping-pong amplification cycle. They associate with PIWI proteins to target and silence transposable elements (TEs), and dysregulation of the PIWI-piRNA pathway has been reported in multiple human cancers. In physiological germline models, epigenetic modifications - including DNA methylation, histone modifications, RNA modifications, and chromatin remodeling - coordinately regulate the activity of piRNA clusters to ensure proper piRNA biogenesis. However, in tumor cells, how epigenetic modifications influence piRNA transcription and processing remains poorly characterized, with most studies focusing on how dysregulated piRNAs drive tumorigenesis via epigenetic or epitranscriptomic mechanisms. This review also discusses species-specific differences, limitations in somatic piRNA annotation, and the evidence needed to distinguish association from mechanism. DNMT/HDAC inhibitors, dietary bioactive compounds, and deactivated Cas9 (dCas9)-based epigenome editing may provide useful experimental or therapeutic approaches, but piRNA-directed epigenetic therapy remains preclinical.
PMID:
43001886
Bibliographic data and abstract were imported from PubMed on 09 Nov 2026.
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