Multi-omics analysis constructs a novel neuroendocrine prostate cancer classifier and classification system

被引:0
作者
Shen, Junxiao [1 ]
Lu, Luyuan [2 ]
Chen, Zujie [1 ]
Guo, Wei [1 ]
Wang, Shuwen [1 ]
Liu, Ziqiao [1 ]
Gong, Xuke [1 ]
Qi, Yiming [1 ]
Jin, Ruyi [3 ]
Zhang, Cheng [1 ]
机构
[1] Zhejiang Univ, Int Inst Med, Sch Med,Int Sch Med, Affiliated Hosp 4,Dept Urol, Yiwu 322000, Peoples R China
[2] Zhejiang Univ, Dept Gen Surg, Int Inst Med, Int Sch Med,Affiliated Hosp 4,Sch Med, Yiwu 322000, Peoples R China
[3] China Med Univ, Dept Dermatol, NHC Key Lab Immunodermatol, Hosp 1, Shenyang 110001, Peoples R China
关键词
Neuroendocrine prostate cancer (NEPC); Multi-omics; Computational biology and bioinformatics; Tumor biomarkers; Tumor heterogeneity; LINEAGE PLASTICITY; EXPRESSION; EVOLUTION; DISCOVERY;
D O I
10.1038/s41598-025-96683-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neuroendocrine prostate cancer (NEPC), a subtype of prostate cancer (PCa) with poor prognosis and high heterogeneity, currently lacks accurate markers. This study aims to identify a robust NEPC classifier and provide new perspectives for resolving intra- tumoral heterogeneity. Multi-omics analysis included 19 bulk transcriptomics, 14 single-cell transcriptomics, 1 spatial transcriptomics, 16 published NE signatures and 10 cellular experiments combined with multiple machine learning algorithms to construct a novel NEPC classifier and classification. A comprehensive single-cell atlas of prostate cancer was created from 70 samples, comprising 196,309 cells, among which 9% were identified as NE cells. Within this framework and in combination with bulk transcriptomics, a total of 100 high-quality NE-specific feature genes were identified and differentiated into NEPup sig and NEPdown sig. The random forest (RF) algorithm proved to be the most effective classifier for NEPC, leading to the establishment of the NEP100 model, which demonstrated robust validation across various datasets. In clinical settings, the use of the NEP100 model can greatly improve the diagnostic and prognostic prediction of NEPC. Hierarchical clustering based on NEP100 revealed four distinct NEPC subtypes, designated VR_O, Prol_N, Prol_P, and EMT_Y, each of which presented unique biological characteristics. This allows us to select different targeted therapeutic strategies for different subtypes of phenotypic pathways. Notably, NEP100 expression correlated positively with neuroendocrine differentiation and disease progression, while the VR-NE phenotype dominated by VR_O cells indicated a propensity for treatment resistance. Furthermore, AMIGO2, a component of the NEP100 signature, was associated with chemotherapy resistance and a poor prognosis, indicating that it is a pivotal target for future therapeutic strategies. This study used multi-omics analysis combined with machine learning to construct a novel NEPC classifier and classification system. NEP100 provides a clinically actionable framework for NEPC diagnosis and subtyping.
引用
收藏
页数:22
相关论文
共 83 条
[61]   Machine learning in medical applications: A review of state-of-the-art methods [J].
Shehab, Mohammad ;
Abualigah, Laith ;
Shambour, Qusai ;
Abu-Hashem, Muhannad A. ;
Shambour, Mohd Khaled Yousef ;
Alsalibi, Ahmed Izzat ;
Gandomi, Amir H. .
COMPUTERS IN BIOLOGY AND MEDICINE, 2022, 145
[62]   Prognostic Utility of a New mRNA Expression Signature of Gleason Score [J].
Sinnott, Jennifer A. ;
Peisch, Sam F. ;
Tyekucheva, Svitlana ;
Gerke, Travis ;
Lis, Rosina ;
Rider, Jennifer R. ;
Fiorentino, Michelangelo ;
Stampfer, Meir J. ;
Mucci, Lorelei A. ;
Loda, Massimo ;
Penney, Kathryn L. .
CLINICAL CANCER RESEARCH, 2017, 23 (01) :81-87
[63]   Enhanced Antitumor Efficacy of Radium-223 and Enzalutamide in the Intratibial LNCaP Prostate Cancer Model [J].
Suominen, Mari I. ;
Knuuttila, Matias ;
Schatz, Christoph A. ;
Schlicker, Andreas ;
Vaaraniemi, Jukka ;
Sjoholm, Birgitta ;
Alhoniemi, Esa ;
Haendler, Bernard ;
Mumberg, Dominik ;
Kakonen, Sanna-Maria ;
Scholz, Arne .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (03)
[64]   Integrative Genomic Profiling of Human Prostate Cancer [J].
Taylor, Barry S. ;
Schultz, Nikolaus ;
Hieronymus, Haley ;
Gopalan, Anuradha ;
Xiao, Yonghong ;
Carver, Brett S. ;
Arora, Vivek K. ;
Kaushik, Poorvi ;
Cerami, Ethan ;
Reva, Boris ;
Antipin, Yevgeniy ;
Mitsiades, Nicholas ;
Landers, Thomas ;
Dolgalev, Igor ;
Major, John E. ;
Wilson, Manda ;
Socci, Nicholas D. ;
Lash, Alex E. ;
Heguy, Adriana ;
Eastham, James A. ;
Scher, Howard I. ;
Reuter, Victor E. ;
Scardino, Peter T. ;
Sander, Chris ;
Sawyers, Charles L. ;
Gerald, William L. .
CANCER CELL, 2010, 18 (01) :11-22
[65]   Gene expression signatures of neuroendocrine prostate cancer and primary small cell prostatic carcinoma [J].
Tsai, Harrison K. ;
Lehrer, Jonathan ;
Alshalalfa, Mohammed ;
Erho, Nicholas ;
Davicioni, Elai ;
Lotan, Tamara L. .
BMC CANCER, 2017, 17
[66]   Resolving the immune landscape of human prostate at a single-cell level in health and cancer [J].
Tuong, Zewen Kelvin ;
Loudon, Kevin W. ;
Berry, Brendan ;
Richoz, Nathan ;
Jones, Julia ;
Tan, Xiao ;
Nguyen, Quan ;
George, Anne ;
Hori, Satoshi ;
Field, Sarah ;
Lynch, Andy G. ;
Kania, Katarzyna ;
Coupland, Paul ;
Babbage, Anne ;
Grenfell, Richard ;
Barrett, Tristan ;
Warren, Anne Y. ;
Gnanapragasam, Vincent ;
Massie, Charlie ;
Clatworthy, Menna R. .
CELL REPORTS, 2021, 37 (12)
[67]   IHC Profiler: An Open Source Plugin for the Quantitative Evaluation and Automated Scoring of Immunohistochemistry Images of Human Tissue Samples [J].
Varghese, Frency ;
Bukhari, Amirali B. ;
Malhotra, Renu ;
De, Abhijit .
PLOS ONE, 2014, 9 (05)
[68]   Neuroendocrine differentiation in prostate cancer: Implications for new treatment modalities [J].
Vashchenko, N ;
Abrahamsson, PA .
EUROPEAN UROLOGY, 2005, 47 (02) :147-155
[69]   Metabolic Reprogramming and Predominance of Solute Carrier Genes during Acquired Enzalutamide Resistance in Prostate Cancer [J].
Verma, Shiv ;
Shankar, Eswar ;
Chan, E. Ricky ;
Gupta, Sanjay .
CELLS, 2020, 9 (12)
[70]   Advances and applications in single-cell and spatial genomics [J].
Wang, Jingjing ;
Ye, Fang ;
Chai, Haoxi ;
Jiang, Yujia ;
Wang, Teng ;
Ran, Xia ;
Xia, Qimin ;
Xu, Ziye ;
Fu, Yuting ;
Zhang, Guodong ;
Wu, Hanyu ;
Guo, Guoji ;
Guo, Hongshan ;
Ruan, Yijun ;
Wang, Yongcheng ;
Xing, Dong ;
Xu, Xun ;
Zhang, Zemin .
SCIENCE CHINA-LIFE SCIENCES, 2025, 68 (05) :1226-1282