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黑覆盆子通过增强结肠上皮和自然杀伤细胞中的 Smad4 表达来抑制结直肠癌。

Black Raspberries Suppress Colorectal Cancer by Enhancing Smad4 Expression in Colonic Epithelium and Natural Killer Cells.

机构信息

Department of Obstetrics & Gynecology, Medical College of Wisconsin, Milwaukee, WI, United States.

Division of Biostatistics, Medical College of Wisconsin, Milwaukee, WI, United States.

出版信息

Front Immunol. 2020 Dec 14;11:570683. doi: 10.3389/fimmu.2020.570683. eCollection 2020.

Abstract

Innate immune cells in the tumor microenvironment have been proposed to control the transition from benign to malignant stages. In many cancers, increased infiltration of natural killer (NK) cells associates with good prognosis. Although the mechanisms that enable NK cells to restrain colorectal cancer (CRC) are unclear, the current study suggests the involvement of Smad4. We found suppressed Smad4 expression in circulating NK cells of untreated metastatic CRC patients. Moreover, NK cell-specific Smad4 deletion promoted colon adenomas in DSS-treated mice and adenocarcinomas in AOM/DSS-treated mice. Other studies have shown that Smad4 loss or weak expression in colonic epithelium associates with poor survival in CRC patients. Therefore, targeting Smad4 in both colonic epithelium and NK cells could provide an excellent opportunity to manage CRC. Toward this end, we showed that dietary intervention with black raspberries (BRBs) increased Smad4 expression in colonic epithelium in patients with FAP or CRC and in the two CRC mouse models. Also, benzoate metabolites of BRBs, such as hippurate, upregulated Smad4 and Gzmb expression that might enhance the cytotoxicity of primary human NK cells. Of note, increased levels of hippurate is a metabolomic marker of a healthy gut microbiota in humans, and hippurate also has antitumor effects. In conclusion, our study suggests a new mechanism for the action of benzoate metabolites derived from plant-based foods. This mechanism could be exploited clinically to upregulate Smad4 in colonic epithelium and NK cells, thereby delaying CRC progression.

摘要

肿瘤微环境中的固有免疫细胞被认为可以控制从良性到恶性阶段的转变。在许多癌症中,自然杀伤 (NK) 细胞的浸润增加与良好的预后相关。尽管 NK 细胞抑制结直肠癌 (CRC) 的机制尚不清楚,但本研究表明 Smad4 的参与。我们发现未经治疗的转移性 CRC 患者循环 NK 细胞中 Smad4 表达受抑制。此外,NK 细胞特异性 Smad4 缺失促进了 DSS 处理的小鼠中的结肠腺瘤和 AOM/DSS 处理的小鼠中的腺癌。其他研究表明,CRC 患者结肠上皮中 Smad4 的缺失或弱表达与不良预后相关。因此,靶向结肠上皮和 NK 细胞中的 Smad4 为管理 CRC 提供了绝佳机会。为此,我们表明,富含鞣花酸的黑莓 (BRBs) 饮食干预可增加 FAP 或 CRC 患者以及两种 CRC 小鼠模型中结肠上皮中的 Smad4 表达。此外,BRBs 的苯甲酸代谢物,如马尿酸,上调 Smad4 和 Gzmb 的表达,这可能增强原代人 NK 细胞的细胞毒性。值得注意的是,马尿酸水平的升高是人类健康肠道微生物群的代谢组学标志物,马尿酸也具有抗肿瘤作用。总之,我们的研究提出了植物源性食物中苯甲酸代谢物作用的新机制。该机制可在临床上用于上调结肠上皮和 NK 细胞中的 Smad4,从而延缓 CRC 的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b2d/7793748/76f1304d309c/fimmu-11-570683-g001.jpg

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