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2 型糖尿病癌症的药物亚表型相互作用。

Drug-subphenotype interactions for cancer in type 2 diabetes mellitus.

机构信息

Department of Epidemiology and Biostatistics, School of Public Health, Tianjin Medical University, 22 Qixiangtai Road, Heping District, Tianjin 300070, China.

Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity, and Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Prince of Wales Hospital, 30-32 Ngan Shing Street, Shatin, New Territories, Hong Kong SAR, China.

出版信息

Nat Rev Endocrinol. 2015 Jun;11(6):372-9. doi: 10.1038/nrendo.2015.37. Epub 2015 Mar 24.

Abstract

On the basis of data obtained from a prospective cohort of Chinese patients with type 2 diabetes mellitus (T2DM), we discuss cancer subphenotypes (risk factors) in patients with T2DM, which can lead to drug-cancer subphenotype interactions. These subphenotypes include HDL cholesterol levels <1.0 mmol/l, co-occurrence of LDL cholesterol levels <2.8 mmol/l and triglyceride levels <1.7 mmol/l, and co-occurrence of LDL cholesterol levels <2.8 mmol/l and albuminuria. The increased risk of cancer associated with low levels of HDL cholesterol, low LDL cholesterol levels plus low triglyceride levels, and low levels of LDL cholesterol plus albuminuria can be reduced by treatment with metformin, renin-angiotensin system (RAS) inhibitors and statins, respectively. Mechanistic studies support the hypothesis that dysregulation of the 5'-AMP-activated protein kinase pathway and crosstalk between the RAS and insulin-like growth factor 1-cholesterol pathways create a cancer-promoting milieu in patients with T2DM. These findings highlight that in Chinese individuals, multiple pathways are implicated in the link between T2DM and cancer, which can generate multiple subphenotypes as well as drug-subphenotype interactions.

摘要

基于中国 2 型糖尿病(T2DM)患者的前瞻性队列研究数据,我们讨论了 T2DM 患者的癌症亚表型(危险因素),这些亚表型可能导致药物-癌症亚表型相互作用。这些亚表型包括高密度脂蛋白胆固醇水平<1.0mmol/L,低密度脂蛋白胆固醇和甘油三酯水平同时<2.8mmol/L 和<1.7mmol/L,以及低密度脂蛋白胆固醇<2.8mmol/L 同时伴有白蛋白尿。用二甲双胍、肾素-血管紧张素系统(RAS)抑制剂和他汀类药物分别治疗可以降低与低水平高密度脂蛋白胆固醇、低水平低密度脂蛋白胆固醇加低水平甘油三酯以及低水平低密度脂蛋白胆固醇加白蛋白尿相关的癌症风险。机制研究支持这样一种假设,即 5'-AMP 激活蛋白激酶途径的失调以及 RAS 和胰岛素样生长因子 1-胆固醇途径之间的串扰在 T2DM 患者中形成了促进癌症的环境。这些发现强调了在中国人群中,多种途径与 T2DM 和癌症之间存在关联,这可能产生多种亚表型以及药物-亚表型相互作用。

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