Molecular analysis of matched PIN , prostate cancer, and adjacent normal prostate tissue reveals distinct transcriptional signatures and recurrent genomic alterations

Prostate intraepithelial neoplasia (PIN) is a recognized precursor to prostate cancer (PCa) and shares many histological and molecular features with invasive disease. To clarify the relationship between PIN and PCa, we performed integrated genomic and transcriptomic analyses on epithelial and stromal laser-capture microdissected samples in matched PIN (n = 121), PCa (n = 217), and adjacent normal (AN, n = 115) prostate tissue from formalin-fixed paraffin-embedded (FFPE) samples across three datasets. We identified two epithelial and two stromal transcriptomic clusters, termed 'invasive-like' and 'normal-like', which were present across all datasets. Among PIN samples, 46% of epithelial and 38% of stromal samples were classified as invasive-like. Whole-genome sequencing analysis revealed recurrent copy number alterations in PIN and PCa lesions, with recurrent copy number alterations more frequently shared between invasive-like PIN and PCa. This study provides new insight into PIN biology and the relationship between PIN and invasive PCa and highlights a transcriptional signature in PIN samples that may have prognostic implications. © 2026 The Pathological Society of Great Britain and Ireland.

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Publication Details

Journal
The Journal of Pathology
Published
2026-10-27
DOI
https://doi.org/10.1002/path.70143
Primary Topic
Prostate Cancer Treatment and Research
Type
article
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article

Molecular analysis of matched PIN , prostate cancer, and adjacent normal prostate tissue reveals distinct transcriptional signatures and recurrent genomic alterations

Rosalie Nolley, Jonathan R. Pollack, Xiaodi Qin, James D. Brooks et al.
The Journal of Pathology
Prostate Cancer Treatment and Research
article

Molecular analysis of matched PIN , prostate cancer, and adjacent normal prostate tissue reveals distinct transcriptional signatures and recurrent genomic alterations

Rosalie Nolley, Jonathan R. Pollack, Xiaodi Qin, James D. Brooks, Gitte Kristensen, Robert B. West, Layne W. Rogers, Chunfang Zhu, Martin Andreas Røder, Christian A. Kunder, Sujay Vennam, Okyaz Eminağa, Sushama Varma, Siri H. Strand, Karina Dalsgaard Sørensen, Jason Wang, Martin Rasmussen
article en

Abstract

Prostate intraepithelial neoplasia (PIN) is a recognized precursor to prostate cancer (PCa) and shares many histological and molecular features with invasive disease. To clarify the relationship between PIN and PCa, we performed integrated genomic and transcriptomic analyses on epithelial and stromal laser-capture microdissected samples in matched PIN (n = 121), PCa (n = 217), and adjacent normal (AN, n = 115) prostate tissue from formalin-fixed paraffin-embedded (FFPE) samples across three datasets. We identified two epithelial and two stromal transcriptomic clusters, termed 'invasive-like' and 'normal-like', which were present across all datasets. Among PIN samples, 46% of epithelial and 38% of stromal samples were classified as invasive-like. Whole-genome sequencing analysis revealed recurrent copy number alterations in PIN and PCa lesions, with recurrent copy number alterations more frequently shared between invasive-like PIN and PCa. This study provides new insight into PIN biology and the relationship between PIN and invasive PCa and highlights a transcriptional signature in PIN samples that may have prognostic implications. © 2026 The Pathological Society of Great Britain and Ireland.

The Journal of Pathology
University of Copenhagen (DK), Oslo University Hospital (NO), Duke University (US), Aarhus University Hospital (DK), Copenhagen University Hospital (DK), Rigshospitalet (DK), Stanford Medicine (US), Duke Cancer Institute (US), Stanford University (US)
Openalex Percentile: Top 12%
Prostate Cancer Treatment and Research
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