Harish K, Dharmalingam M, Himanshu M
Department of Surgical Oncology, M, S, Ramaiah Medical College & Hospital, Bangalore 560054, India.
BMC Endocr Disord. 2007 Oct 22;7:10. doi: 10.1186/1472-6823-7-10.
Studies have shown that metabolic syndrome and its consequent biochemical derangements in the various phases of diabetes may contribute to carcinogenesis. A part of this carcinogenic effect could be attributed to hyperinsulinism. High levels of insulin decrease the production of IGF-1 binding proteins and hence increase levels of free IGF-1. It is well established that bioactivity of free insulin growth factor 1 (IGF-1) increases tumor turnover rate. The objective is to investigate the role of insulin resistance/sensitivity in carcinogenesis by studying the relation between insulin resistance/sensitivity and IGF-1 levels in cancer patients. We postulate that hyperinsulinaemia which prevails during initial phases of insulin resistance (condition prior to overt diabetes) increases bioactivity of free IGF-1, which may contribute to process of carcinogenesis.
METHODS/DESIGN: Based on our pilot study results and power analysis of the same, we have designed a two group case-control study. 800 proven untreated cancer patients (solid epithelial cell tumors) under age of 50 shall be recruited with 200 healthy subjects serving as controls. Insulin resistance/sensitivity and free IGF-1 levels shall be determined in all subjects. Association between the two parameters shall be tested using suitable statistical methods.
Well controlled studies in humans are essential to study the link between insulin resistance, hyperinsulinaemia, IGF-1 and carcinogenesis. This study could provide insights to the role of insulin, insulin resistance, IGF-1 in carcinogenesis although a precise role and the extent of influence cannot be determined. In future, cancer prevention and treatment strategies could revolve around insulin and insulin resistance.
研究表明,代谢综合征及其在糖尿病各阶段随之出现的生化紊乱可能促进癌症发生。这种致癌作用的一部分可能归因于高胰岛素血症。高水平的胰岛素会降低胰岛素样生长因子-1(IGF-1)结合蛋白的产生,从而提高游离IGF-1的水平。众所周知,游离胰岛素生长因子1(IGF-1)的生物活性会提高肿瘤周转率。目的是通过研究癌症患者胰岛素抵抗/敏感性与IGF-1水平之间的关系,探讨胰岛素抵抗/敏感性在癌症发生中的作用。我们推测,在胰岛素抵抗初始阶段(显性糖尿病之前的状态)普遍存在的高胰岛素血症会增加游离IGF-1的生物活性,这可能有助于癌症发生过程。
方法/设计:基于我们的初步研究结果及其功效分析,我们设计了一项两组病例对照研究。将招募800名经证实未接受治疗的50岁以下癌症患者(实体上皮细胞瘤),并选取200名健康受试者作为对照。测定所有受试者的胰岛素抵抗/敏感性和游离IGF-1水平。使用合适的统计方法检验这两个参数之间的关联。
对人类进行严格控制的研究对于研究胰岛素抵抗、高胰岛素血症、IGF-1与癌症发生之间的联系至关重要。尽管无法确定胰岛素、胰岛素抵抗、IGF-1在癌症发生中的精确作用和影响程度,但本研究可以为它们在癌症发生中的作用提供见解。未来,癌症预防和治疗策略可能围绕胰岛素和胰岛素抵抗展开。