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Changes in circulating small non-coding RNAs after castration in a cohort of prostate cancer patients
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  • Published: 03 February 2026

Changes in circulating small non-coding RNAs after castration in a cohort of prostate cancer patients

  • Ailsa Maria Main1,2,3,
  • Louise Holst Sørensen1,3,
  • Sofia Boeg Winge1,3,
  • Mikkel Fode4,5,
  • Jens Sønksen4,5,
  • Anders Juul1,3,5,
  • Peter Busch Østergren4,5,
  • Nina Mørup1,3 &
  • …
  • Kristian Almstrup1,2,3 

Scientific Reports , Article number:  (2026) Cite this article

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Cancer
  • Molecular biology
  • Urology

Abstract

Small non-coding RNAs (sncRNAs) can be found in circulation and may carry endocrine signals. Here, we analyse circulating sncRNAs before and after castration to identify sncRNAs that potentially could convey endocrine signals from the testis. In a previous randomized clinical trial, men with advanced prostate cancer (n = 57) were treated by either subcapsular orchiectomy (O-arm, n = 28) or GnRH-analogue (G-arm, n = 29). Blood samples were obtained at baseline (W0) and at 12 (W12) and 24 weeks (W24) post-intervention. Small non-coding RNAs from 169 longitudinally paired serum samples were sequenced using the RealSeq-Biofluids Small RNA kit. A joint analysis of sncRNA reads at W12 and W24 compared to W0 identified 81 and 175 circulating sncRNAs present at significantly (FDR < 0.05) different levels in the O-arm and G-arm, respectively. Most sncRNAs were found at lower levels after treatment (n = 67 (83%) and n = 150 (86%) in the O- and G-arm, respectively). The most prevalent type of sncRNA was piRNAs contributing to 44% (n = 36 piRNAs) in the O-arm and 58% (n = 101 piRNAs) in the G-arm. When the two treatment arms were analysed together, 16 sncRNAs were found to be consistently altered after castration. Of these sncRNAs, 8 were piRNAs and 4 have previously been reported in the testis, indicating a likely testicular origin. Using RT-qPCR and small RNA in situ hybridisation, we validated a testicular expression of miR-153 and SNORD38A. In conclusion, the circulating sncRNA profiles are altered after castration and with a substantial loss of piRNAs indicating lost secretion of testicular sncRNAs. However, we cannot deduce if these circulating piRNAs mediate an endocrine signal.

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Data availability

The small RNA sequencing data in this study have been deposited in the European Nucleotide Archive (ENA; [https://www.ebi.ac.uk/ena/]) at EMBL-EBI under accession number PRJEB106978.

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Funding

Novo Nordisk Foundation (grant numbers NNF210C0069913 and NNF21C0069969 to KA), the Svend Andersen Foundation, and the Independent Research Fund (grant number: 1030-0381B to KA).

Author information

Authors and Affiliations

  1. Department of Growth and Reproduction, Copenhagen University Hospital - Rigshospitalet, Blegdamsvej 9, 2100, Copenhagen, Denmark

    Ailsa Maria Main, Louise Holst Sørensen, Sofia Boeg Winge, Anders Juul, Nina Mørup & Kristian Almstrup

  2. Department of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark

    Ailsa Maria Main & Kristian Almstrup

  3. International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health, Copenhagen, Denmark

    Ailsa Maria Main, Louise Holst Sørensen, Sofia Boeg Winge, Anders Juul, Nina Mørup & Kristian Almstrup

  4. Department of Urology, Copenhagen University Hospital – Herlev and Gentofte, Herlev, Denmark

    Mikkel Fode, Jens Sønksen & Peter Busch Østergren

  5. Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark

    Mikkel Fode, Jens Sønksen, Anders Juul & Peter Busch Østergren

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Contributions

KA, NM and AMM designed the study. AMM, KA and NM collected, analysed and interpreted the data. LS and SW did qPCR and in situ hybridization. AMM, KA, LS, and SW wrote the manuscript. PØ, MF, JS and AJ provided materials for analysis and specialist knowledge. All authors contributed to the final editing of the manuscript.

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Correspondence to Ailsa Maria Main or Kristian Almstrup.

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MF has been speaker and advisory board member of Astellas Pharma. All other authors have nothing to disclose.

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Main, A.M., Sørensen, L.H., Winge, S.B. et al. Changes in circulating small non-coding RNAs after castration in a cohort of prostate cancer patients. Sci Rep (2026). https://doi.org/10.1038/s41598-026-38334-9

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  • Received: 02 September 2025

  • Accepted: 29 January 2026

  • Published: 03 February 2026

  • DOI: https://doi.org/10.1038/s41598-026-38334-9

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Keywords

  • Small RNA sequencing
  • Castration
  • Endocrine biomarkers
  • Testis
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