Department of Surgery, Geisel School of Medicine at Dartmouth, Norris Cotton Cancer Center, Lebanon, New Hampshire, USA.
Department of Medicine, Geisel School of Medicine at Dartmouth, Norris Cotton Cancer Center, Lebanon, New Hampshire, USA.
Br J Clin Pharmacol. 2023 Mar;89(3):1027-1035. doi: 10.1111/bcp.15546. Epub 2022 Oct 12.
Metformin is used for the management of type 2 diabetes mellitus (T2DM) and is being tested clinically as an anticancer agent. Metformin concentrations safely achievable in human solid tissues including tumours are unknown. This study was designed to determine metformin concentration in tissue compartments as a function of dose to inform rational dosing in preclinical models and interpretation of clinical results."
Subjects with solid tumours to be treated by resection and either (A) willingness to take metformin for 7-10 days before surgery or (B) taking metformin for T2DM were eligible. Whole blood, plasma, tumour, tumour-adjacent uninvolved tissue and subcutaneous adipose tissue were obtained for liquid chromatography with tandem mass spectrometry to measure metformin concentrations.
All subjects had primary lung tumours. Metformin dose was significantly correlated with drug concentrations in all tissues analysed. Intersubject metformin concentrations varied by over two orders of magnitude. Metformin concentrations were significantly higher in tumour tissues and lower in adipose tissues compared to other tissues. Concentrations in blood and plasma were significantly correlated with concentrations in solid tissues.
Metformin accumulates in cellular compartments. Concentrations observed in plasma, blood, lung and tumour tissues in subjects treated with US Food and Drug Administration-approved doses for T2DM are lower than those typically used in tissue culture studies. However, such tissue concentrations are in line with those found within cultured cells treated with supra-pharmacological doses of metformin. Given the large intersubject variability in metformin concentrations, it is imperative to determine whether there is an association between tissue metformin concentration and anticancer activity in humans.
二甲双胍用于治疗 2 型糖尿病(T2DM),并正在临床测试作为一种抗癌药物。目前尚不清楚在包括肿瘤在内的人类实体组织中安全达到的二甲双胍浓度。本研究旨在确定组织隔室中二甲双胍浓度与剂量的关系,以为临床前模型中的合理给药提供信息,并解释临床结果。
符合以下条件的患有实体瘤的受试者可入选进行切除术治疗,并且(A)愿意在手术前服用二甲双胍 7-10 天,或者(B)患有 T2DM 并正在服用二甲双胍。采集全血、血浆、肿瘤、肿瘤相邻未受累组织和皮下脂肪组织,用于液相色谱-串联质谱法测量二甲双胍浓度。
所有受试者均患有原发性肺癌。二甲双胍剂量与所有分析组织中的药物浓度显著相关。受试者间的二甲双胍浓度差异超过两个数量级。与其他组织相比,肿瘤组织中的二甲双胍浓度明显较高,脂肪组织中的浓度较低。血液和血浆中的浓度与固体组织中的浓度显著相关。
二甲双胍在细胞隔室中积累。在接受美国食品和药物管理局批准的 T2DM 治疗剂量的受试者中,血浆、血液、肺部和肿瘤组织中观察到的二甲双胍浓度低于组织培养研究中通常使用的浓度。然而,这些组织浓度与用超药理学剂量的二甲双胍处理的培养细胞中发现的浓度一致。鉴于二甲双胍浓度在受试者间存在很大的变异性,必须确定人体组织中二甲双胍浓度与抗癌活性之间是否存在关联。