2 型糖尿病患者的胰岛素治疗与癌症。

ISRN endocrinology Pub Date : 2012-01-01 Epub Date: 2012-11-14 DOI:10.5402/2012/240634
Edoardo Mannucci
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引用次数: 0

摘要

尽管有许多其他药物,胰岛素仍被广泛用作治疗 2 型糖尿病的药物。在体外,胰岛素通过与胰岛素样生长因子-1(IGF-1)受体和自身受体相互作用,刺激癌细胞生长。在有关 2 型糖尿病的观察性调查中,胰岛素治疗与几种癌症发病率的增加有关,但很难将混杂因素的影响与胰岛素本身的影响区分开来。随机试验并不能证实胰岛素治疗会增加风险,但也不能排除胰岛素治疗对某些癌症的负面影响,至少在剂量较大时是如此。在胰岛素类似物中,格列宁与 IGF-1 受体的亲和力更高,体外促有丝分裂的效力也比人胰岛素强,但它在体外被广泛代谢为 IGF-1 受体亲和力低的产物。总体而言,流行病学研究表明,与人胰岛素相比,格列卫可能会增加患癌风险,但仅限于高剂量和某些形式的癌症(如乳腺癌)。临床试验数据并未证实,但仍不足以完全排除这种风险增加的可能性。不过,胰岛素的益处大于潜在的癌症风险。
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Insulin therapy and cancer in type 2 diabetes.

Despite the availability of many other agents, insulin is widely used as a treatment for type 2 diabetes. In vitro, insulin stimulates the growth of cancer cells, through the interaction with insulin-like growth factor-1 (IGF-1) receptors and its own receptors. In observational surveys on type 2 diabetes, insulin therapy is associated with an increased incidence of several forms of cancer, although it is difficult to discriminate the effect of confounders from that of insulin itself. Randomized trials do not confirm the increased risk associated with insulin therapy, although they do not allow to rule out some negative effects on specific forms of cancer, at least at higher doses. Among insulin analogues, glargine has a higher affinity for the IGF-1 receptor and a greater mitogenic potency in vitro than human insulin, but it is extensively metabolized in vitro to products with low IGF-1 receptor affinity. Overall, epidemiological studies suggest a possible increase of risk with glargine, with respect to human insulin, only at high doses and for some forms of cancer (i.e., breast). Data from clinical trials do not confirm, but are still insufficient to totally exclude, such increased risk. However, beneficial effects of insulin outweigh potential cancer risks.

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