snFLARE-seq and mrFRIGID for the transcriptomic and metabolomic landscape of prostate cancer with different anatomical origins

前列腺癌 代谢组学 转录组 疾病 癌症 计算生物学 医学 代谢物 前列腺 生物信息学 癌细胞 生物 癌症研究 肿瘤微环境 临床意义 代谢组 肿瘤科 循环肿瘤细胞 内科学 生物标志物 生物标志物发现
作者
Li Zhenfei,xiaokai20220628
出处
期刊:CERN European Organization for Nuclear Research - Zenodo [European Organization for Nuclear Research]
标识
DOI:10.5281/zenodo.17779236
摘要

snFLARE-seq and mrFRIGID for the transcriptomic and metabolomic landscape of prostate cancer with different anatomical origins Prostate cancer cells of different anatomical locations display remarkable heterogeneity. This poses a challenge to the clinical relevance of pre-clinical models and the efficacy of contemporary therapeutic approaches. Here we developed the snFLARE-seq and mrFRIGID methodologies to directly investigate the transcriptomic and metabolomic landscape of prostate cancer patients utilizing formalin-fixed paraffin-embedded (FFPE) specimens. A retrospective analysis revealed the clinical disparities of prostate cancer from peripheral zone (PZ), transition zone (TZ), and across PZ and TZ. The snFLARE-seq, refined for enhanced single-nucleus sequencing, unveiled distinct cell type distributions and signaling pathways between PZ and TZ samples. Hormone therapy substantially affected cancer cells and microenvironment, leading to a polarized feature of epithelial cells and a subverted immune microenvironment. With improvements on metabolite extraction, mrFRIGID revealed unique metabolic features of prostate cancer from different origins. The metabolomic results indicate that PZ cancer cells were in a metabolic-dormant status, which were probably awaken by hormone therapy. Integrative analysis of results from snFLARE-seq, mrFRIGID, and TCGA database uncovered four metabolic pathways and related genes associated with disease aggressiveness. Our work would accelerate investigations on disease heterogeneity and evolution in real-world clinical settings, stimulating patient-specific precision healthcare solutions. This study utilized the Dynamic Network Biomarkers (DNB) model developed by ChenLab at the Chinese Academy of Sciences (CAS) to analyze single-cell data. For specific details, please visit https://github.com/Kaiyu-W/DNBr. To install this package, use the following command in R: devtools::install_github("Kaiyu-W/DNBr") The associated datasets are publicly available at Zenodo under the following persistent link: https://zenodo.org/records/15671856

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