Saxena Arpit, Chumanevich Alexander, Fletcher Emma, Larsen Bianca, Lattwein Kirby, Kaur Kamaljeet, Fayad Raja
Department of Exercise Science, Arnold School of Public Health, University of South Carolina, Columbia, South Carolina, 921 Assembly Street, Room 402, USA.
Biochim Biophys Acta. 2012 Apr;1822(4):527-36. doi: 10.1016/j.bbadis.2011.12.006. Epub 2011 Dec 16.
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) (20mg/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.
脂联素(APN)是一种脂肪因子,在葡萄糖和脂质代谢中发挥作用,具有抗炎和抗癌活性,其缺失与包括结直肠癌在内的几种肥胖相关恶性肿瘤有关。本研究的目的是确定APN缺乏对慢性炎症诱导的结肠癌的影响。这是通过在APN基因敲除(KO)小鼠和C57B1/6野生型(WT)小鼠中诱导炎症和结肠癌来实现的。它们被分为四个治疗组(n = 6):1)对照组(不治疗);2)用三个周期的葡聚糖硫酸钠(DSS)治疗;3)每周剂量的1,2 - 二甲基肼(DMH)(20mg/kg小鼠体重),持续十二周;4)单次剂量的DMH,然后进行3个周期的DSS(DMH + DSS)。观察小鼠的腹泻、粪便潜血和体重减轻情况,并在第153天处死。计算肿瘤面积和数量。收集结肠组织进行蛋白质印迹和免疫组织化学分析。在第一个DSS周期中,APN KO小鼠比WT小鼠更能抵抗DSS诱导的结肠炎,但在第二个和第三个DSS周期中失去了这种保护作用。APN KO小鼠有明显更严重的症状,并且与WT小鼠相比,肿瘤数量更多、面积更大,免疫细胞浸润和炎症更严重。蛋白质组学研究通过蛋白质印迹和免疫组织化学对pSTAT3、pAMPK和Cox - 2进行分析,进一步证实了这一结果。总之,APN缺乏会导致炎症诱导的结肠癌。因此,APN可能通过调节参与慢性炎症和肿瘤发生的基因在结直肠癌预防中发挥重要作用。