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高脂饮食诱导的炎症通过 IL6 信号加速前列腺癌生长。

High-Fat Diet-Induced Inflammation Accelerates Prostate Cancer Growth via IL6 Signaling.

机构信息

Department of Urology, Osaka University Graduate School of Medicine, Suita, Japan.

Department of Pathology, Osaka University Graduate School of Medicine, Suita, Japan.

出版信息

Clin Cancer Res. 2018 Sep 1;24(17):4309-4318. doi: 10.1158/1078-0432.CCR-18-0106. Epub 2018 May 18.

Abstract

High-fat diet (HFD) could induce prostate cancer progression. The aim of this study is to identify mechanisms of HFD-induced prostate cancer progression, focusing on inflammation. We administered HFD and celecoxib to autochthonous immunocompetent Pb-Cre;(fl/fl) model mice for prostate cancer. Tumor growth was evaluated by tumor weight and Ki67 stain, and local immune cells were assessed by flow cytometry at 22 weeks of age. Cytokines which correlated with tumor growth were identified, and the changes of tumor growth and local immune cells after inhibition of the cytokine signals were evaluated in the mice. IHC analyses using prostatectomy specimens of obese patients were performed. HFD accelerated tumor growth and increased the myeloid-derived suppressor cells (MDSCs) fraction and M2/M1 macrophage ratio in the model mice. Celecoxib-suppressed tumor growth, and decreased both local MDSCs and M2/M1 macrophage ratio in HFD-fed mice. HFD-induced tumor growth was associated with IL6 secreted by prostatic macrophages, as were phosphorylated STAT3 (pSTAT3)-positive tumor cells. Anti-IL6 receptor antibody administration suppressed tumor growth, and decreased local MDSCs and pSTAT3-positive cell fractions in HFD-fed mice. The tumor-infiltrating CD11b-positive cell count was significantly higher in prostatectomy specimens of obese than those of nonobese patients with prostate cancer. HFD increased MDSCs and accelerated prostate cancer tumor growth via IL6/pSTAT3 signaling in the mice. This mechanism could exist in obese patients with prostate cancer. IL6-mediated inflammation could be a therapeutic target for prostate cancer. .

摘要

高脂肪饮食(HFD)可诱导前列腺癌进展。本研究旨在确定 HFD 诱导前列腺癌进展的机制,重点关注炎症。我们给自发免疫 competent Pb-Cre;(fl/fl)模型小鼠喂食 HFD 和塞来昔布以诱导前列腺癌。在 22 周龄时,通过肿瘤重量和 Ki67 染色评估肿瘤生长,通过流式细胞术评估局部免疫细胞。鉴定与肿瘤生长相关的细胞因子,并在抑制细胞因子信号后评估其对肿瘤生长和局部免疫细胞的影响。对肥胖患者的前列腺切除术标本进行了免疫组化分析。HFD 加速了肿瘤生长,并增加了模型小鼠中的髓系来源抑制细胞(MDSCs)分数和 M2/M1 巨噬细胞比例。塞来昔布抑制了肿瘤生长,并降低了 HFD 喂养小鼠的局部 MDSCs 和 M2/M1 巨噬细胞比例。HFD 诱导的肿瘤生长与前列腺巨噬细胞分泌的 IL6 以及磷酸化 STAT3(pSTAT3)阳性肿瘤细胞有关。抗 IL6 受体抗体的给药抑制了肿瘤生长,并降低了 HFD 喂养小鼠的局部 MDSCs 和 pSTAT3 阳性细胞分数。肥胖患者前列腺切除术标本中的肿瘤浸润性 CD11b 阳性细胞计数明显高于非肥胖患者。HFD 通过 IL6/pSTAT3 信号增加了 MDSCs 并加速了小鼠前列腺癌肿瘤的生长。这种机制可能存在于肥胖的前列腺癌患者中。IL6 介导的炎症可能是前列腺癌的治疗靶点。

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