Transcriptional analysis of metastatic hormone-naïve prostate cancer primary tumor biopsies reveals a relevant role for SOX11 in prostate cancer cell dissemination.
[BACKGROUND] Metastatic hormone-naïve prostate cancer (mHNPC) is an infrequent form of this tumor type that is characterized by metastasis at the time of diagnosis and accounts for up to 50% of prosta
APA
Martin-Martin N, Garcia-Longarte S, et al. (2025). Transcriptional analysis of metastatic hormone-naïve prostate cancer primary tumor biopsies reveals a relevant role for SOX11 in prostate cancer cell dissemination.. Genome biology, 26(1), 154. https://doi.org/10.1186/s13059-025-03623-5
MLA
Martin-Martin N, et al.. "Transcriptional analysis of metastatic hormone-naïve prostate cancer primary tumor biopsies reveals a relevant role for SOX11 in prostate cancer cell dissemination.." Genome biology, vol. 26, no. 1, 2025, pp. 154.
PMID
40462200
Abstract
[BACKGROUND] Metastatic hormone-naïve prostate cancer (mHNPC) is an infrequent form of this tumor type that is characterized by metastasis at the time of diagnosis and accounts for up to 50% of prostate cancer-related deaths. Despite the extensive characterization of localized and metastatic castration-resistant prostate cancer, the molecular characteristics of mHNPC remain largely unexplored.
[RESULTS] Here, we provide the first extensive transcriptomics characterization of primary tumor specimens from patients with mHNPC. We generate discovery and validation bulk and single-cell RNA-seq datasets and perform integrative computational analysis in combination with experimental studies. Our results provide unprecedented evidence of the distinctive transcriptional profile of mHNPC and identify stroma remodeling as a predominant feature of these tumors. Importantly, we discover a central role for the SRY-box transcription factor 11 (SOX11) in triggering a heterotypic communication that is associated with the acquisition of metastatic properties.
[CONCLUSIONS] Our study will constitute an invaluable resource for a profound understanding of mHNPC that can influence patient management.
[RESULTS] Here, we provide the first extensive transcriptomics characterization of primary tumor specimens from patients with mHNPC. We generate discovery and validation bulk and single-cell RNA-seq datasets and perform integrative computational analysis in combination with experimental studies. Our results provide unprecedented evidence of the distinctive transcriptional profile of mHNPC and identify stroma remodeling as a predominant feature of these tumors. Importantly, we discover a central role for the SRY-box transcription factor 11 (SOX11) in triggering a heterotypic communication that is associated with the acquisition of metastatic properties.
[CONCLUSIONS] Our study will constitute an invaluable resource for a profound understanding of mHNPC that can influence patient management.
MeSH Terms
Male; Humans; SOXC Transcription Factors; Prostatic Neoplasms; Neoplasm Metastasis; Gene Expression Regulation, Neoplastic; Transcriptome; Biopsy; Cell Line, Tumor