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.
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页数:22
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共 83 条
[1]   Genomic correlates of clinical outcome in advanced prostate cancer [J].
Abida, Wassim ;
Cyrta, Joanna ;
Heller, Glenn ;
Prandi, Davide ;
Armenia, Joshua ;
Coleman, Ilsa ;
Cieslik, Marcin ;
Benelli, Matteo ;
Robinson, Dan ;
Van Allen, Eliezer M. ;
Sboner, Andrea ;
Fedrizzi, Tarcisio ;
Mosquera, Juan Miguel ;
Robinson, Brian D. ;
De Sarkar, Navonil ;
Kunju, Lakshmi P. ;
Tomlins, Scott ;
Wu, Yi Mi ;
Rodrigues, Daniel Nava ;
Loda, Massimo ;
Gopalan, Anuradha ;
Reuter, Victor E. ;
Pritchard, Colin C. ;
Mateo, Joaquin ;
Bianchini, Diletta ;
Miranda, Susana ;
Carreira, Suzanne ;
Rescigno, Pasquale ;
Filipenko, Julie ;
Vinson, Jacob ;
Montgomery, Robert B. ;
Beltran, Himisha ;
Heath, Elisabeth I. ;
Scher, Howard I. ;
Kantoff, Philip W. ;
Taplin, Mary-Ellen ;
Schultz, Nikolaus ;
deBono, Johann S. ;
Demichelis, Francesca ;
Nelson, Peter S. ;
Rubin, Mark A. ;
Chinnaiyan, Arul M. ;
Sawyers, Charles L. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 116 (23) :11428-11436
[2]   Clinical and Genomic Characterization of Treatment-Emergent Small-Cell Neuroendocrine Prostate Cancer: A Multi-institutional Prospective Study [J].
Aggarwal, Rahul ;
Huang, Jiaoti ;
Alumkal, Joshi J. ;
Zhang, Li ;
Feng, Felix Y. ;
Thomas, George V. ;
Weinstein, Alana S. ;
Friedl, Verena ;
Zhang, Can ;
Witte, Owen N. ;
Lloyd, Paul ;
Gleave, Martin ;
Evans, Christopher P. ;
Youngren, Jack ;
Beer, Tomasz M. ;
Rettig, Matthew ;
Wong, Christopher K. ;
True, Lawrence ;
Foye, Adam ;
Playdle, Denise ;
Ryan, Charles J. ;
Lara, Primo ;
Chi, Kim N. ;
Uzunangelov, Vlado ;
Sokolov, Artem ;
Newton, Yulia ;
Beltran, Himisha ;
Demichelis, Francesca ;
Rubin, Mark A. ;
Stuart, Joshua M. ;
Small, Eric J. .
JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (24) :2492-+
[3]   Characterization of transcriptomic signature of primary prostate cancer analogous to prostatic small cell neuroendocrine carcinoma [J].
Alshalalfa, Mohammed ;
Liu, Yang ;
Wyatt, Alexander W. ;
Gibb, Ewan A. ;
Tsai, Harrison K. ;
Erho, Nicholas ;
Lehrer, Jonathan ;
Takhar, Mandeep ;
Ramnarine, Varune R. ;
Collins, Colin C. ;
Den, Robert B. ;
Schaeffer, Edward M. ;
Davicioni, Elai ;
Lotan, Tamara L. ;
Bismar, Tarek A. .
INTERNATIONAL JOURNAL OF CANCER, 2019, 145 (12) :3453-3461
[4]   Transcriptional profiling identifies an androgen receptor activity-low, stemness program associated with enzalutamide resistance [J].
Alumkal, Joshi J. ;
Sun, Duanchen ;
Lu, Eric ;
Beer, Tomasz M. ;
Thomas, George V. ;
Latour, Emile ;
Aggarwal, Rahul ;
Cetnar, Jeremy ;
Ryan, Charles J. ;
Tabatabaei, Shaadi ;
Bailey, Shawna ;
Turina, Claire B. ;
Quigley, David A. ;
Guan, Xiangnan ;
Foye, Adam ;
Youngren, Jack F. ;
Urrutia, Joshua ;
Huang, Jiaoti ;
Weinstein, Alana S. ;
Friedl, Verena ;
Rettig, Matthew ;
Reiter, Robert E. ;
Spratt, Daniel E. ;
Gleave, Martin ;
Evans, Christopher P. ;
Stuart, Joshua M. ;
Chen, Yiyi ;
Feng, Felix Y. ;
Small, Eric J. ;
Witte, Owen N. ;
Xia, Zheng .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2020, 117 (22) :12315-12323
[5]   Integrative Molecular Analyses of the MD Anderson Prostate Cancer Patient-derived Xenograft (MDA PCa PDX) Series [J].
Anselmino, Nicolas ;
Labanca, Estefania ;
Shepherd, Peter D. A. ;
Dong, Jiabin ;
Yang, Jun ;
Song, Xiaofei ;
Nandakumar, Subhiksha ;
Kundra, Ritika ;
Lee, Cindy ;
Schultz, Nikolaus ;
Zhang, Jianhua ;
Araujo, John C. ;
Aparicio, Ana M. ;
Subudhi, Sumit K. ;
Corn, Paul G. ;
Pisters, Louis L. ;
Ward, John F. ;
Davis, John W. ;
Vazquez, Elba S. ;
Gueron, Geraldine ;
Logothetis, Christopher J. ;
Futreal, Andrew ;
Troncoso, Patricia ;
Chen, Yu ;
Navone, Nora M. .
CLINICAL CANCER RESEARCH, 2024, 30 (10) :2272-2285
[6]   Androgen Receptor Signaling Pathway in Prostate Cancer: From Genetics to Clinical Applications [J].
Aurilio, Gaetano ;
Cimadamore, Alessia ;
Mazzucchelli, Roberta ;
Lopez-Beltran, Antonio ;
Verri, Elena ;
Scarpelli, Marina ;
Massari, Francesco ;
Cheng, Liang ;
Santoni, Matteo ;
Montironi, Rodolfo .
CELLS, 2020, 9 (12)
[7]   SCLC Subtypes Defined by ASCL1, NEUROD1, POU2F3, and YAP1: A Comprehensive Immunohistochemical and Histopathologic Characterization [J].
Baine, Marina K. ;
Hsieh, Min-Shu ;
Lai, W. Victoria ;
Egger, Jacklynn V. ;
Jungbluth, Achim A. ;
Daneshbod, Yahya ;
Beras, Amanda ;
Spencer, Rowanne ;
Lopardo, Jessica ;
Bodd, Francis ;
Montecalvo, Joseph ;
Sauter, Jennifer L. ;
Chang, Jason C. ;
Buonocore, Darren J. ;
Travis, William D. ;
Sen, Triparna ;
Poirier, John T. ;
Rudin, Charles M. ;
Rekhtman, Natasha .
JOURNAL OF THORACIC ONCOLOGY, 2020, 15 (12) :1823-1835
[8]   Divergent clonal evolution of castration-resistant neuroendocrine prostate cancer [J].
Beltran, Himisha ;
Prandi, Davide ;
Mosquera, Juan Miguel ;
Benelli, Matteo ;
Puca, Loredana ;
Cyrta, Joanna ;
Marotz, Clarisse ;
Giannopoulou, Eugenia ;
Chakravarthi, Balabhadrapatruni V. S. K. ;
Varambally, Sooryanarayana ;
Tomlins, Scott A. ;
Nanus, David M. ;
Tagawa, Scott T. ;
Van Allen, Eliezer M. ;
Elemento, Olivier ;
Sboner, Andrea ;
Garraway, Levi A. ;
Rubin, Mark A. ;
Demichelis, Francesca .
NATURE MEDICINE, 2016, 22 (03) :298-305
[9]   Stem cell dynamics and cellular heterogeneity across lineage subtypes of castrate-resistant prostate cancer [J].
Beshiri, Michael L. ;
Capaldo, Brian J. ;
Lake, Ross ;
Ku, Anson T. ;
Burner, Danielle ;
Tice, Caitlin M. ;
Tran, Crystal ;
Kostas, Julianna ;
Alilin, Aian Neil ;
Yin, Juanjuan ;
Agarwal, Supreet ;
Morris, Samantha A. ;
Karzai, Fatima H. ;
Lotan, Tamara L. ;
Dahut, William L. ;
Sowalsky, Adam G. ;
Kelly, Kathleen .
STEM CELLS, 2024, 42 (06) :526-539
[10]   Androgen Receptor Pathway-Independent Prostate Cancer Is Sustained through FGF Signaling [J].
Bluemn, Eric G. ;
Coleman, Ilsa M. ;
Lucas, Jared M. ;
Coleman, Roger T. ;
Hernandez-Lopez, Susana ;
Tharakan, Robin ;
Bianchi-Frias, Daniella ;
Dumpit, Ruth F. ;
Kaipainen, Arja ;
Corella, Alexandra N. ;
Yang, Yu Chi ;
Nyquist, Michael D. ;
Mostaghel, Elahe ;
Hsieh, Andrew C. ;
Zhang, Xiaotun ;
Corey, Eva ;
Brown, Lisha G. ;
Nguyen, Holly M. ;
Pienta, Kenneth ;
Ittmann, Michael ;
Schweizer, Michael ;
True, Lawrence D. ;
Wise, David ;
Rennie, Paul S. ;
Vessella, Robert L. ;
Morrissey, Colm ;
Nelson, Peter S. .
CANCER CELL, 2017, 32 (04) :474-+