Overexpression of miR-17-5p may negatively impact p300/CBP factor-associated inflammation in a hypercholesterolemic advanced prostate cancer model

Background Previously, we demonstrated that cholesterol triggers the increase in p300/CBP-associated factor (PCAF), targeted by miR-17-5p. The p300, IL-6, PCAF, and miR-17-5p genes have important and contradictory roles in inflammation and prostate cancer (PCa). This study aimed to demonstrate the p...

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Veröffentlicht in:Molecular biology reports 2023-09, Vol.50 (9), p.7333-7345
Hauptverfasser: Pimenta, Ruan, Camargo, Juliana A., Gonçalves, Guilherme L., Ghazarian, Vitória, Candido, Patrícia, Guimarães, Vanessa R., Romão, Poliana, Chiovatto, Caroline, da Silva, Karina Serafim, dos Santos, Gabriel A., Silva, Iran A., Nahas, William C., Leite, Kátia R., Pessoa, Ana Flávia Marçal, Viana, Nayara I., Reis, Sabrina T.
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Sprache:eng
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Zusammenfassung:Background Previously, we demonstrated that cholesterol triggers the increase in p300/CBP-associated factor (PCAF), targeted by miR-17-5p. The p300, IL-6, PCAF, and miR-17-5p genes have important and contradictory roles in inflammation and prostate cancer (PCa). This study aimed to demonstrate the potential anti-inflammatory effect of miR-17-5 in an advanced PCa model with diet-induced hypercholesterolemia. Methods and results In vitro, using the PC-3 cell line, we show that induction of miR-17-5p reduces p300 and PCAF expression, increases apoptosis, and decreases cell migration. Furthermore, we demonstrate that supplementing this same cell with cholesterol (2 µg/mL) triggers increased p300, IL-6, and PCAF. In vivo, after establishing the hypercholesterolemic (HCOL) model, xenografts were treated with miR-17-5p. Increased expression of this miR after intratumoral injections attenuated tumor growth in the control and HCOL animals and reduced cell proliferation. Conclusion Our results demonstrate that inducing miR-17-5p expression suppresses tumor growth and inflammatory mediator expression. Further studies should be conducted to fully explore the role of miR-17-5p and the involvement of inflammatory mediators p300, PCAF, and IL-6.
ISSN:0301-4851
1573-4978
DOI:10.1007/s11033-023-08638-4