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Individual Comparison of Cholesterol Metabolism in Normal and Tumour Areas in Radical Prostatectomy Specimens from Patients with Prostate Cancer: Results of the CHOMECAP Study

Authors :
Jean-Marc A. Lobaccaro
Claudio Caccia
Olivier Celhay
Laura Bousset
Amalia Trousson
Cyrille de Joussineau
Jean-Louis Kemeny
Christelle Damon-Soubeyrant
Laurent Guy
Laurent Morel
Angélique De Haze
Silvère Baron
Valerio Leoni
Bruno Pereira
Laura Sabourin
Catherine Godfraind
Celhay, O
Bousset, L
Guy, L
Kemeny, J
Leoni, V
Caccia, C
Trousson, A
Damon-Soubeyrant, C
De Haze, A
Sabourin, L
Godfraind, C
de Joussineau, C
Pereira, B
Morel, L
Lobaccaro, J
Baron, S
Génétique, Reproduction et Développement (GReD)
Centre National de la Recherche Scientifique (CNRS)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Institut National de la Santé et de la Recherche Médicale (INSERM)
Imagerie Moléculaire et Stratégies Théranostiques (IMoST)
Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Institut National de la Santé et de la Recherche Médicale (INSERM)
Cancer Resistance Exploring and Targeting (CREaT)
Université d'Auvergne - Clermont-Ferrand I (UdA)
Laboratory of Clinical Pathology and Medical Genetics
Fondazione IRCCS Istituto Neurologico 'Carlo Besta'
University of Groningen [Groningen]
CHU Clermont-Ferrand
service de Biostatistiques, DRCI
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Centre National de la Recherche Scientifique (CNRS)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])
Source :
European Urology Oncology, European Urology Oncology, Elsevier, 2019, 2 (2), pp.198-206. ⟨10.1016/j.euo.2018.08.001⟩, European Urology Oncology, 2019, 2 (2), pp.198-206. ⟨10.1016/j.euo.2018.08.001⟩
Publication Year :
2019
Publisher :
Elsevier B.V., 2019.

Abstract

International audience; BACKGROUND: Deregulation of cholesterol metabolism represents a hallmark of prostate cancer (PCa) and promotes its development. OBJECTIVE: To compare cholesterol metabolism on individual paired normal and tumour prostate tissues obtained from patients with PCa. DESIGN, SETTING, AND PARTICIPANTS: Between 2008 and 2012, normal and tumour paired tissue samples were collected from radical prostatectomy specimens from a cohort of 69 patients treated for localised PCa. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Tumour and normal tissues were subjected to gene analysis, sterol measurement, and immunohistochemistry. The Wilcoxon paired test and Spearman test were applied for comparison and correlation analyses, respectively. Principal component analysis was also carried out to investigate relationships between quantitative variables. RESULTS AND LIMITATIONS: Overall, cholesterol concentrations were not significantly different between tissue pairs. However, tumour samples were significantly associated with downregulated de novo cholesterol synthesis, but exhibited 54.7% overexpression of SCARB1 that could increase high-density lipoprotein uptake in PCa. Tumour tissues showed different trafficking of available cholesterol, with significantly lower ACAT1, and an altered efflux via APOE. Furthermore, cholesterol metabolism in tumour tissues was characterised by higher accumulation of 7alpha-hydroxycholesterol (OHC), 7betaOHC, and 7-ketosterol, and a lower level of 27OHC. CONCLUSIONS: Focusing on individually paired prostate tissues, our results highlighted several differences between normal and tumour samples linked to a metabolic shift in cholesterol flux. PCa samples exhibited a specific tissue signature characterised by higher SCARB1 expression, higher accumulation of OHC species, and clear downregulation of de novo cholesterol synthesis. PATIENT SUMMARY: Comparing normal and tumour tissues from the same prostates, our study identified a set of alterations in prostate cancer samples in terms of their use of cholesterol. These included higher cholesterol uptake, accumulation of oxidised cholesterol derivatives, and autonomous cellular production of cholesterol. Together, these data provide promising clinical targets to fight prostate cancer.

Details

Language :
English
ISSN :
25889311
Database :
OpenAIRE
Journal :
European Urology Oncology, European Urology Oncology, Elsevier, 2019, 2 (2), pp.198-206. ⟨10.1016/j.euo.2018.08.001⟩, European Urology Oncology, 2019, 2 (2), pp.198-206. ⟨10.1016/j.euo.2018.08.001⟩
Accession number :
edsair.doi.dedup.....33024b6465c8988fc4f14d1bf63f3ff1