Integrative proteomic and phosphoproteomic profiling of prostate cell lines

Autoři: Maria Katsogiannou aff001;  Jean-Baptiste Boyer aff001;  Alberto Valdeolivas aff003;  Elisabeth Remy aff003;  Laurence Calzone aff006;  Stéphane Audebert aff001;  Palma Rocchi aff001;  Luc Camoin aff001;  Anaïs Baudot aff003
Působiště autorů: Aix Marseille Univ, CNRS, INSERM, Institut Paoli-Calmettes, CRCM, Marseille, France aff001;  Obstetrics and Gynecology department, Hôpital Saint Joseph, Marseille, France aff002;  Aix Marseille Univ, CNRS, Centrale Marseille, I2M, Marseille, France aff003;  Aix Marseille Univ, INSERM, MMG, Marseille, France aff004;  ProGeLife, Marseille, France aff005;  Mines Paris Tech, Institut Curie, PSL Research University, Paris, France aff006
Vyšlo v časopise: PLoS ONE 14(11)
Kategorie: Research Article
doi: 10.1371/journal.pone.0224148



Prostate cancer is a major public health issue, mainly because patients relapse after androgen deprivation therapy. Proteomic strategies, aiming to reflect the functional activity of cells, are nowadays among the leading approaches to tackle the challenges not only of better diagnosis, but also of unraveling mechanistic details related to disease etiology and progression.


We conducted here a large SILAC-based Mass Spectrometry experiment to map the proteomes and phosphoproteomes of four widely used prostate cell lines, namely PNT1A, LNCaP, DU145 and PC3, representative of different cancerous and hormonal status.


We identified more than 3000 proteins and phosphosites, from which we quantified more than 1000 proteins and 500 phosphosites after stringent filtering. Extensive exploration of this proteomics and phosphoproteomics dataset allowed characterizing housekeeping as well as cell-line specific proteins, phosphosites and functional features of each cell line. In addition, by comparing the sensitive and resistant cell lines, we identified protein and phosphosites differentially expressed in the resistance context. Further data integration in a molecular network highlighted the differentially expressed pathways, in particular migration and invasion, RNA splicing, DNA damage repair response and transcription regulation.


Overall, this study proposes a valuable resource toward the characterization of proteome and phosphoproteome of four widely used prostate cell lines and reveals candidates to be involved in prostate cancer progression for further experimental validation.

Klíčová slova:

Biomarkers – Membrane proteins – Phosphorylation – Prostate cancer – Protein expression – Proteomes – Proteomic databases – DU145 cells


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