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高胆固醇血症晚期前列腺癌模型中 miR-17-5p 的过表达可能对 p300/CBP 因子相关炎症产生负面影响。

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

机构信息

Laboratorio de Investigação Médica 55 (LIM55), Faculdade de Medicina, Hospital das Clinicas HCFMUSP, Universidade de Sao Paulo, Av. Dr. Arnaldo 455, 2° floor, room 2145, Sao Paulo, Sao Paulo, SP, BR, SP, 01246- 903, Brazil.

D'Or Institute for Research and Education (IDOR), Sao Paulo, Brazil.

出版信息

Mol Biol Rep. 2023 Sep;50(9):7333-7345. doi: 10.1007/s11033-023-08638-4. Epub 2023 Jul 13.

Abstract

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.

摘要

背景

此前,我们证明胆固醇可触发 miR-17-5p 靶向的 p300/CBP 相关因子(PCAF)增加。p300、IL-6、PCAF 和 miR-17-5p 基因在炎症和前列腺癌(PCa)中具有重要且相互矛盾的作用。本研究旨在证明 miR-17-5 在饮食诱导的高胆固醇血症所致晚期 PCa 模型中的潜在抗炎作用。

方法和结果

在体外,使用 PC-3 细胞系,我们表明诱导 miR-17-5p 可降低 p300 和 PCAF 的表达,增加细胞凋亡并减少细胞迁移。此外,我们证明向同一细胞补充胆固醇(2μg/ml)可触发 p300、IL-6 和 PCAF 增加。在体内,建立高胆固醇血症(HCOL)模型后,用 miR-17-5p 处理异种移植物。肿瘤内注射后该 miR 的表达增加可减轻对照和 HCOL 动物的肿瘤生长并减少细胞增殖。

结论

我们的结果表明,诱导 miR-17-5p 的表达可抑制肿瘤生长和炎症介质的表达。应进一步进行研究以充分探讨 miR-17-5p 的作用以及炎症介质 p300、PCAF 和 IL-6 的参与。

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