A186 炎症改变肠道抗肿瘤小鼠对蔓越莓原花青素及其微生物代谢产物 3-(4-羟基苯基)丙酸的剂量依赖性反应

Z. Dimoff, Z. Lofft, F. Liang, S Chen, I. Paetau-Robinson, C. Khoo, A. Taibi, E. Comelli
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Aims To determine if miR-146a-5p and miR-363-3p respond to different physiologically relevant concentrations of PAC and HPPA in inflammatory and non-inflammatory conditions. Methods Fully differentiated Caco-2BBe1 colonic epithelial cells were treated with two doses of PAC-enriched cranberry extract (50μg/ml, 100μg/ml), HPPA (5μg/ml, 10μg/ml), or with Dulbecco’s Modified Eagle Medium (DMEM; control) for 24 hours, followed by IL-1β (1ng/ml) or mock stimulation for three hours. Human IL-6 homogeneous time-resolved fluorescence (HTRF) kits were used to quantify IL-6 in cell supernatant. RNA was extracted and used for miRNA profiling using Nanostring technology. Statistical analysis was performed in R version 4.2.1 with the R-packages NanostringDiff, NanostringNorm, and Pheatmap. Results At homeostasis, 42 and 2 (miR-146a and miR363-3p) miRNAs, respectively, uniquely responded to increasing PAC or HPPA concentrations. In the inflammatory state, no miRNAs responded to increasing concentrations of PAC and HPPA. However, the expression of miR-363-3p increased (qampersand:003C0.001) in response to 50μg/ml of PAC + IL-1β but decreased in response to 5μg/ml of HPPA + IL-1β , and the expression of miR-146a-5p increased (qampersand:003C0.001) in response to 5μg/ml of HPPA + IL-1β, and 50μg/ml PAC + IL-1β. Predicted miRNA gene-pathway analysis revealed that miR-146a-5p, miR-363-3p, and the other 42 miRNAs commonly target pathways involved in the tumorigenesis of colorectal cancer such as mitogen-activated protein kinases (MAPK), hedgehog, and Wnt pathways. Though, in inflamed cells, only HPPA (5 or 10 μg/ml) attenuated IL-6 secretion (pampersand:003C0.05), which may be driven by increased expression of miR-146a-5p. 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引用次数: 0

摘要

摘要 背景 蔓越莓是一种具有抗癌特性的多酚--原花青素(PAC)的丰富来源。我们以前曾发现,PAC 及其微生物衍生的代谢物 3-(4-羟基苯基)丙酸(HPPA)会触发肠上皮细胞中微小核糖核酸(miRNA)的独特调控反应,包括上调 miR-146a-5p。miR-146a-5p 和 miR363-3p 都具有抗炎作用,可分别下调白细胞介素(IL)-17 和无翼鸟相关整合位点(Wnt)等抗肿瘤信号通路。目的 确定在炎症和非炎症条件下,miR-146a-5p 和 miR-363-3p 是否会对不同生理相关浓度的 PAC 和 HPPA 产生反应。方法 用两种剂量的富含 PAC 的蔓越莓提取物(50μg/ml、100μg/ml)、HPPA(5μg/ml、10μg/ml)或 Dulbecco's Modified Eagle Medium(DMEM;对照)处理完全分化的 Caco-2BBe1 结肠上皮细胞 24 小时,然后用 IL-1β(1ng/ml)或模拟刺激处理 3 小时。使用人 IL-6 均相时间分辨荧光(HTRF)试剂盒定量检测细胞上清液中的 IL-6。提取 RNA 并使用 Nanostring 技术进行 miRNA 分析。统计分析使用 R 软件包 NanostringDiff、NanostringNorm 和 Pheatmap 在 4.2.1 版中进行。结果 在平衡状态下,分别有 42 个和 2 个(miR-146a 和 miR363-3p)miRNA 对 PAC 或 HPPA 浓度的增加有独特的反应。在炎症状态下,没有 miRNA 对 PAC 和 HPPA 浓度的增加有反应。然而,miR-363-3p 的表达在 PAC + IL-1β 浓度为 50μg/ml 时增加(qampersand:003C0.001),但在 HPPA + IL-1β 浓度为 5μg/ml 时减少;miR-146a-5p 的表达在 HPPA + IL-1β 浓度为 5μg/ml 和 PAC + IL-1β 浓度为 50μg/ml 时增加(qampersand:003C0.001)。预测的 miRNA 基因通路分析表明,miR-146a-5p、miR-363-3p 和其他 42 个 miRNA 通常靶向参与结直肠癌肿瘤发生的通路,如丝裂原活化蛋白激酶(MAPK)、刺猬和 Wnt 通路。不过,在发炎细胞中,只有 HPPA(5 或 10 μg/ml)能减少 IL-6 的分泌(pampersand:003C0.05),这可能是由于 miR-146a-5p 的表达增加所致。结论 这些研究结果表明,蔓越莓原花青素及其代谢物以不同的方式和浓度影响参与癌症相关途径的 miRNA,这可能取决于炎症状态。肠道微生物群可能是产生这些影响的部分原因。资助机构:Ocean Spray 小红莓公司和加拿大自然科学与工程研究理事会(NSERC)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A186 INFLAMMATION MODIFIES DOSE-DEPENDENT RESPONSES OF INTESTINAL ANTI-TUMOUR MICRORNAS TO CRANBERRY PROANTHOCYANIDIN AND ITS MICROBIAL METABOLITE 3-(4-HYDROXYPHENYL)-PROPIONIC ACID
Abstract Background Cranberries are a rich source of proanthocyanidins (PAC), a type of polyphenol with anti-cancer properties. We previously found that PAC, along with its microbially-derived metabolite 3-(4-hydroxyphenyl)-propionic acid (HPPA), trigger unique regulatory responses of microRNAs (miRNAs) in intestinal epithelial cells including the upregulation of miR-146a-5p. Both miR-146a-5p and miR363-3p are anti-inflammatory and downregulate anti-tumorigenic signalling pathways such as the interleukin (IL)-17 and wingless-related integration site (Wnt) respectively. miR-146a-5p also attenuates IL-17-promoting cytokines levels (e.g., IL-6). Aims To determine if miR-146a-5p and miR-363-3p respond to different physiologically relevant concentrations of PAC and HPPA in inflammatory and non-inflammatory conditions. Methods Fully differentiated Caco-2BBe1 colonic epithelial cells were treated with two doses of PAC-enriched cranberry extract (50μg/ml, 100μg/ml), HPPA (5μg/ml, 10μg/ml), or with Dulbecco’s Modified Eagle Medium (DMEM; control) for 24 hours, followed by IL-1β (1ng/ml) or mock stimulation for three hours. Human IL-6 homogeneous time-resolved fluorescence (HTRF) kits were used to quantify IL-6 in cell supernatant. RNA was extracted and used for miRNA profiling using Nanostring technology. Statistical analysis was performed in R version 4.2.1 with the R-packages NanostringDiff, NanostringNorm, and Pheatmap. Results At homeostasis, 42 and 2 (miR-146a and miR363-3p) miRNAs, respectively, uniquely responded to increasing PAC or HPPA concentrations. In the inflammatory state, no miRNAs responded to increasing concentrations of PAC and HPPA. However, the expression of miR-363-3p increased (qampersand:003C0.001) in response to 50μg/ml of PAC + IL-1β but decreased in response to 5μg/ml of HPPA + IL-1β , and the expression of miR-146a-5p increased (qampersand:003C0.001) in response to 5μg/ml of HPPA + IL-1β, and 50μg/ml PAC + IL-1β. Predicted miRNA gene-pathway analysis revealed that miR-146a-5p, miR-363-3p, and the other 42 miRNAs commonly target pathways involved in the tumorigenesis of colorectal cancer such as mitogen-activated protein kinases (MAPK), hedgehog, and Wnt pathways. Though, in inflamed cells, only HPPA (5 or 10 μg/ml) attenuated IL-6 secretion (pampersand:003C0.05), which may be driven by increased expression of miR-146a-5p. Conclusions These findings suggest that cranberries proanthocyanidins and their metabolites affect miRNAs involved in cancer related pathways in different manners and concentrations, which may depend on the inflammatory status. The gut microbiota may be partially responsible for unlocking these effects. Funding Agencies Ocean Spray Cranberries, Inc. and the Natural Sciences of Engineering Research Council of Canada (NSERC)
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