Department of Medicine, St. Hedwig Hospital, Grosse Hamburger Strasse 5-11, D-10115 Berlin, Germany.
J Clin Endocrinol Metab. 2012 Apr;97(4):E510-20. doi: 10.1210/jc.2011-1754. Epub 2012 Jan 25.
Hyperinsulinemia and insulin resistance are the major reasons for a higher prevalence of several cancer entities in type 2 diabetes mellitus and obesity. Metformin exerts a growth-inhibitory effect by reducing hyperinsulinemia and by a direct cellular action.
We investigated the effect of metformin on growth of differentiated human thyroid cells, anaplastic thyroid carcinoma cells, a doxorubicin-resistant thyroid carcinoma cell line, and thyroid cancer stem cells.
The antimitogenic effect of metformin was studied in thyroid cells derived from goiters and in thyroid carcinoma cell lines by analysis of cell growth, cell cycle progression, and apoptosis. Furthermore, the influence of pretreatment with insulin or with chemotherapeutic agents on metformin-induced growth inhibition was investigated in thyroid carcinoma cells, in a doxorubicin-resistant thyroid carcinoma cell line, and in derived carcinoma stem cells.
Metformin showed an antimitogenic effect by inhibition of cell cycle progression and induction of apoptosis. In addition, metformin antagonized the growth-stimulatory effect of insulin, inhibited clonal cell growth, reduced thyroid cancer sphere formation, and potentiated the antimitogenic effect of chemotherapeutic agents such as doxorubicin and cisplatin on undifferentiated thyroid carcinoma cells. Remarkably, the antiproliferative effect of metformin was even found in a doxorubicin-resistant thyroid carcinoma cell line. The growth-inhibitory effect of metformin was, however, not restricted to differentiated thyroid cells and undifferentiated thyroid carcinoma cells but was also demonstrated in thyroid carcinoma cancer stem cells.
Metformin markedly diminished growth stimulation by insulin and showed an additive antimitogenic effect to chemotherapeutics agents. Therefore, our results suggest this drug as adjuvant treatment for thyroid cancer in type 2 diabetic patients.
高胰岛素血症和胰岛素抵抗是 2 型糖尿病和肥胖症中多种癌症实体患病率较高的主要原因。二甲双胍通过降低高胰岛素血症和直接细胞作用发挥生长抑制作用。
我们研究了二甲双胍对分化的人甲状腺细胞、间变性甲状腺癌细胞、多柔比星耐药甲状腺癌细胞系和甲状腺癌干细胞生长的影响。
通过分析细胞生长、细胞周期进程和细胞凋亡,研究了二甲双胍对甲状腺肿来源的甲状腺细胞和甲状腺癌细胞系的抗有丝分裂作用。此外,还研究了胰岛素或化疗药物预处理对甲状腺癌细胞、多柔比星耐药甲状腺癌细胞系和衍生的癌干细胞中二甲双胍诱导的生长抑制的影响。
二甲双胍通过抑制细胞周期进程和诱导细胞凋亡表现出抗有丝分裂作用。此外,二甲双胍拮抗胰岛素的促生长作用,抑制克隆细胞生长,减少甲状腺癌细胞球形成,并增强多柔比星和顺铂等化疗药物对未分化甲状腺癌细胞的抗有丝分裂作用。值得注意的是,二甲双胍的增殖抑制作用甚至在多柔比星耐药甲状腺癌细胞系中也存在。二甲双胍的生长抑制作用不仅限于分化的甲状腺细胞和未分化的甲状腺癌细胞,而且在甲状腺癌干细胞中也得到了证明。
二甲双胍显著减弱了胰岛素的生长刺激作用,并表现出与化疗药物的相加抗有丝分裂作用。因此,我们的研究结果表明,这种药物可作为 2 型糖尿病甲状腺癌患者的辅助治疗。