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脂联素对结肠癌的有益作用:在小鼠体内和体外的研究。

Salutary effects of adiponectin on colon cancer: in vivo and in vitro studies in mice.

机构信息

Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02130, USA.

出版信息

Gut. 2013 Apr;62(4):561-70. doi: 10.1136/gutjnl-2012-302092. Epub 2012 Jun 26.

Abstract

BACKGROUND

Obesity and a high-fat diet are associated with the risk and progression of colon cancer. Low adiponectin levels may play an important role in the development of colon and other obesity-related malignancies. No previous studies have directly investigated the mechanistic effects of adiponectin on colon cancer in the settings of obesity, a high-fat diet and/or adiponectin deficiency.

OBJECTIVE

To investigate the effects of adiponectin on the growth of colorectal cancer in adiponectin-deficient or wild-type-C57BL/6 mice fed a low-fat or high-fat diet.

RESULTS

Mice fed a high-fat-diet gained more weight and had larger tumours than mice fed a low-fat-diet. Adiponectin administration suppressed implanted tumour growth, causing larger central necrotic areas. Adiponectin treatment also suppressed angiogenesis assessed by CD31 staining and VEGFb and VEGFd mRNA expression in tumours obtained from mice fed a high-fat-diet and from adiponectin-deficient mice. Adiponectin treatment decreased serum insulin levels in mice on a high-fat-diet and increased serum-interleukin (IL)-12 levels in adiponectin-deficient mice. In vitro, it was found that adiponectin directly controls malignant potential (cell proliferation, adhesion, invasion and colony formation) and regulates metabolic (AMPK/S6), inflammatory (STAT3/VEGF) and cell cycle (p21/p27/p53/cyclins) signalling pathways in both mouse MCA38 and human HT29, HCT116 and LoVo colon cancer cell lines in a LKB1-dependent way.

CONCLUSION

These new mechanistic and pathophysiology studies provide evidence for an important role of adiponectin in colon cancer. The data indicate that adiponectin or analogues might be useful agents in the management or chemoprevention of colon cancer.

摘要

背景

肥胖和高脂肪饮食与结肠癌的风险和进展相关。低脂联素水平可能在结肠癌和其他肥胖相关恶性肿瘤的发生发展中发挥重要作用。既往研究尚未直接探讨脂联素在肥胖、高脂肪饮食和/或脂联素缺乏情况下对结肠癌的作用机制。

目的

研究脂联素在低脂饮食或高脂饮食喂养的脂联素缺乏型或野生型 C57BL/6 小鼠中对结直肠癌细胞生长的影响。

结果

高脂饮食组小鼠体重增加更多,肿瘤更大。脂联素给药抑制了植入肿瘤的生长,导致更大的中央坏死区。脂联素治疗还抑制了 CD31 染色和肿瘤中 VEGFb 和 VEGFd mRNA 表达评估的血管生成,这些肿瘤来自高脂饮食喂养的小鼠和脂联素缺乏型小鼠。脂联素治疗降低了高脂饮食组小鼠的血清胰岛素水平,并增加了脂联素缺乏型小鼠的血清白细胞介素(IL)-12 水平。在体外,发现脂联素通过 LKB1 依赖性方式直接控制恶性潜能(细胞增殖、黏附、侵袭和集落形成),并调节代谢(AMPK/S6)、炎症(STAT3/VEGF)和细胞周期(p21/p27/p53/细胞周期蛋白)信号通路,在小鼠 MCA38 和人 HT29、HCT116 和 LoVo 结肠癌细胞系中均如此。

结论

这些新的机制和病理生理学研究为脂联素在结肠癌中的重要作用提供了证据。数据表明,脂联素或类似物可能是结肠癌管理或化学预防的有用药物。

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