Proteomic-based stratification of intermediate-risk prostate cancer patients

Author:

Zhong Qing1ORCID,Sun Rui23,Aref Adel T1ORCID,Noor Zainab1,Anees Asim1,Zhu Yi23,Lucas Natasha1ORCID,Poulos Rebecca C1,Lyu Mengge23,Zhu Tiansheng23,Chen Guo-Bo4ORCID,Wang Yingrui23,Ding Xuan23,Rutishauser Dorothea5ORCID,Rupp Niels J5,Rueschoff Jan H5,Poyet Cédric6ORCID,Hermanns Thomas6,Fankhauser Christian67,Rodríguez Martínez María8ORCID,Shao Wenguang9,Buljan Marija1011,Neumann Janis Frederick12,Beyer Andreas12ORCID,Hains Peter G1ORCID,Reddel Roger R1ORCID,Robinson Phillip J1,Aebersold Ruedi1314ORCID,Guo Tiannan23ORCID,Wild Peter J1516ORCID

Affiliation:

1. ProCan, Children’s Medical Research Institute

2. iMarker Lab, Westlake Laboratory of Life Sciences and Biomedicine, Key Laboratory of Structural Biology of Zhejiang Province, School of Life Sciences, Westlake University

3. Institute of Basic Medical Sciences, Westlake Institute for Advanced Study, Hangzhou, China

4. Urology & Nephrology Center, Department of Urology, Clinical Research Institute, Zhejiang Provincial People’s Hospital, People’s Hospital of Hangzhou Medical College, Hangzhou, China

5. Department of Pathology and Molecular Pathology, University Hospital Zürich, Zürich, Switzerland

6. Department of Urology, University Hospital Zürich, Zürich, Switzerland

7. Department of Urology, Cantonal Hospital Lucerne, Lucerne, Switzerland

8. IBM Zürich Research Laboratory, Zürich, Switzerland

9. State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic and Developmental Sciences, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China

10. Empa - Swiss Federal Laboratories for Materials Science and Technology, St. Gallen, Switzerland

11. Swiss Institute of Bioinformatics, Lausanne, Switzerland

12. CECAD, University of Cologne, Cologne, Germany

13. Department of Biology, Institute of Molecular Systems Biology, ETH Zürich, Zürich, Switzerland

14. Faculty of Science, University of Zürich, Zürich, Switzerland

15. Goethe University Frankfurt, Dr. Senckenberg Institute of Pathology, University Hospital Frankfurt

16. Frankfurt Institute for Advanced Studies, Frankfurt am Main, Germany

Abstract

Gleason grading is an important prognostic indicator for prostate adenocarcinoma and is crucial for patient treatment decisions. However, intermediate-risk patients diagnosed in the Gleason grade group (GG) 2 and GG3 can harbour either aggressive or non-aggressive disease, resulting in under- or overtreatment of a significant number of patients. Here, we performed proteomic, differential expression, machine learning, and survival analyses for 1,348 matched tumour and benign sample runs from 278 patients. Three proteins (F5, TMEM126B, and EARS2) were identified as candidate biomarkers in patients with biochemical recurrence. Multivariate Cox regression yielded 18 proteins, from which a risk score was constructed to dichotomize prostate cancer patients into low- and high-risk groups. This 18-protein signature is prognostic for the risk of biochemical recurrence and completely independent of the intermediate GG. Our results suggest that markers generated by computational proteomic profiling have the potential for clinical applications including integration into prostate cancer management.

Funder

EC | Horizon 2020 Framework Programme

Bundesministerium für Bildung und Forschung

National Natural Science Foundation of China

SNSF SystemsX.ch fellowship

National Key Research and Development Program of China

NHMRC Fellowships

National Breast Cancer Foundation

European Commission’s Horizon 2020 Program

National Health and Medical Research Council

Cancer Council NSW

NSW Ministry of Health

Cancer Institute New South Wales

Publisher

Life Science Alliance, LLC

Subject

Health, Toxicology and Mutagenesis,Plant Science,Biochemistry, Genetics and Molecular Biology (miscellaneous),Ecology

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