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Variable effects of periprostatic adipose tissue on prostate cancer cells: Role of adipose tissue lipid composition and cancer cells related factors.
Cancel, Mathilde; Crottes, David; Bellanger, Dorine; Bruyère, Frank; Mousset, Coralie; Pinault, Michelle; Mahéo, Karine; Fromont, Gaëlle.
Affiliation
  • Cancel M; Faculté de Médecine, Inserm UMR1069 "Nutrition, Croissance et Cancer" Université François Rabelais, Tours, France.
  • Crottes D; Department of Medical Oncology, CHU Tours, Tours, France.
  • Bellanger D; Faculté de Médecine, Inserm UMR1069 "Nutrition, Croissance et Cancer" Université François Rabelais, Tours, France.
  • Bruyère F; Faculté de Médecine, Inserm UMR1069 "Nutrition, Croissance et Cancer" Université François Rabelais, Tours, France.
  • Mousset C; Department of Urology, CHU Tours, Tours, France.
  • Pinault M; Faculté de Médecine, Inserm UMR1069 "Nutrition, Croissance et Cancer" Université François Rabelais, Tours, France.
  • Mahéo K; Department of Pathology, CHU Tours, Tours, France.
  • Fromont G; Faculté de Médecine, Inserm UMR1069 "Nutrition, Croissance et Cancer" Université François Rabelais, Tours, France.
Prostate ; 84(4): 358-367, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38112233
ABSTRACT

BACKGROUND:

Periprostatic adipose tissue (PPAT) is likely to modulate prostate cancer (PCa) progression. We analyzed the variations in the effect of PPAT on cancer cells, according to its fatty acid (FA) composition and tumor characteristics.

METHODS:

The expression of markers of aggressiveness Ki67 and Zeb1, and epigenetic marks that could be modified during PCa progression, was analyzed by immunohistochemistry on a tissue-micro-array containing 59 pT3 PCa, including intra-prostatic areas and extra-prostatic foci in contact with PPAT belonging to the same tumor. In addition, we cocultivated PC3 and LNCaP cell lines with PPAT, which were then analyzed for FA composition.

RESULTS:

Although the contact between PPAT and cancer cells led overall to an increase in Ki67 and Zeb1, and a decrease in the epigenetic marks 5MC, 5HMC, and H3K27ac, these effects were highly heterogeneous. Increased proliferation in extra-prostatic areas was associated with the international society of uropathology score. PC3 and LNCaP cocultures with PPAT led to increased Ki67, Zeb1 and H3K27me3, but only for PPAT associated with aggressive PCa. PC3 proliferation was correlated with high 20.2 n-6 and low 20.5n-3 in PPAT.

CONCLUSIONS:

These results suggest that the effects of PPAT on cancer cells may depend on both PCa characteristics and PPAT composition, and could lead to propose nutritional supplementation.
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Full text: 1 Database: MEDLINE Main subject: Prostatic Neoplasms Language: En Journal: Prostate Year: 2024 Type: Article Affiliation country: France

Full text: 1 Database: MEDLINE Main subject: Prostatic Neoplasms Language: En Journal: Prostate Year: 2024 Type: Article Affiliation country: France