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首页> 外文期刊>Biochimica et biophysica acta. Molecular basis of disease: BBA >Adiponectin deficiency: Role in chronic inflammation induced colon cancer
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Adiponectin deficiency: Role in chronic inflammation induced colon cancer

机译:脂联素缺乏症:在慢性炎症诱导的结肠癌中的作用

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Adiponectin (APN), an adipokine, exerts an anti-inflammatory and anti-cancerous activity with its role in glucose and lipid metabolism and its absence related to several obesity related malignancies including colorectal cancer. The aim of this study is to determine the effect of APN deficiency on the chronic inflammation-induced colon cancer. This was achieved by inducing inflammation and colon cancer in both APN knockout (KO) and C57B1/6 wild type (WT) mice. They were divided into four treatment groups (n=6): 1) control (no treatment); 2) treatment with three cycles of dextran sodium sulfate (DSS); 3) weekly doses of 1,2-dimethylhydrazine (DMH) (20. mg/kg of mouse body weight) for twelve weeks; 4) a single dose of DMH followed by 3 cycles of DSS (DMH. +. DSS). Mice were observed for diarrhea, stool hemoccult, and weight loss and were sacrificed on day 153. Tumor area and number were counted. Colonic tissues were collected for Western blot and immunohistochemistry analyses. APNKO mice were more protected than WT mice from DSS induced colitis during first DSS cycle, but lost this protection during the second and the third DSS cycles. APNKO mice had significantly severe symptoms and showed greater number and larger area of tumors with higher immune cell infiltration and inflammation than WT mice. This result was further confirmed by proteomic study including pSTAT3, pAMPK and Cox-2 by western blot and Immunohistochemistry. Conclusively, APN deficiency contributes to inflammation-induced colon cancer. Hence, APN may play an important role in colorectal cancer prevention by modulating genes involved in chronic inflammation and tumorigenesis.
机译:脂联素(APN)是一种脂肪因子,在葡萄糖和脂质代谢中起着抗炎和抗癌的作用,并且不与包括肥胖症在内的多种肥胖相关的恶性肿瘤有关。这项研究的目的是确定APN缺乏对慢性炎症引起的结肠癌的影响。这是通过在APN基因敲除(KO)和C57B1 / 6野生型(WT)小鼠中诱导炎症和结肠癌实现的。他们分为四个治疗组(n = 6):1)对照组(不治疗); 2)用三个循环的葡聚糖硫酸钠(DSS)处理; 3)每周服用1,2-二甲基肼(DMH)(20. mg / kg小鼠体重),持续十二周; 4)单一剂量的DMH,然后进行3个周期的DSS(DMH。+。DSS)。观察小鼠的腹泻,便血和体重减轻,并在第153天处死。计数肿瘤面积和数目。收集结肠组织用于蛋白质印迹和免疫组织化学分析。在第一个DSS周期中,APNKO小鼠比WT小鼠受到DSS诱导的结肠炎的保护更大,但在第二个和第三个DSS周期中失去了这种保护。与野生型小鼠相比,APNKO小鼠具有明显的严重症状,并显示出更大数量和更大面积的肿瘤以及更高的免疫细胞浸润和炎症。蛋白质组学研究进一步证实了这一结果,包括蛋白质印迹研究,免疫印迹和免疫组织化学分析,包括pSTAT3,pAMPK和Cox-2。总之,APN缺乏会导致炎症诱发的结肠癌。因此,APN可能通过调节与慢性炎症和肿瘤发生有关的基因,在预防大肠癌中发挥重要作用。

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