Seabloom Donna E, Galbraith Arthur R, Haynes Anna M, Antonides Jennifer D, Wuertz Beverly R, Miller Wendy A, Miller Kimberly A, Steele Vernon E, Miller Mark Steven, Clapper Margie L, O'Sullivan M Gerard, Ondrey Frank G
Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
AeroCore Inhalation Testing, College of Pharmacy, University of Minnesota, Minneapolis, Minnesota.
Cancer Prev Res (Phila). 2017 Feb;10(2):116-123. doi: 10.1158/1940-6207.CAPR-16-0232. Epub 2017 Jan 4.
Combination treatment with pioglitazone and metformin is utilized clinically in the treatment of type II diabetes. Treatment with this drug combination reduced the development of aerodigestive cancers in this patient population. Our goal is to expand this treatment into clinical lung cancer chemoprevention. We hypothesized that dietary delivery of metformin/pioglitazone would prevent lung adenoma formation in A/J mice in a benzo[a]pyrene (B[a]P)-induced carcinogenesis model while modulating chemoprevention and anti-inflammatory biomarkers in residual adenomas. We found that metformin (500 and 850 mg/kg/d) and pioglitazone (15 mg/kg/d) produced statistically significant decreases in lung adenoma formation both as single-agent treatments and in combination, compared with untreated controls, after 15 weeks. Treatment with metformin alone and in combination with pioglitazone resulted in statistically significant decreases in lung adenoma formation at both early- and late-stage interventions. Pioglitazone alone resulted in significant decreases in adenoma formation only at early treatment intervention. We conclude that oral metformin is a viable chemopreventive treatment at doses ranging from 500 to 1,000 mg/kg/d. Pioglitazone at 15 mg/kg/d is a viable chemopreventive agent at early-stage interventions. Combination metformin and pioglitazone performed equal to metformin alone and better than pioglitazone at 15 mg/kg/d. Because the drugs are already FDA-approved, rapid movement to human clinical studies is possible. Cancer Prev Res; 10(2); 116-23. ©2017 AACR.
吡格列酮和二甲双胍联合治疗在临床上用于治疗II型糖尿病。该药物组合治疗可降低该患者群体中气道消化道癌症的发生。我们的目标是将这种治疗扩展到临床肺癌化学预防。我们假设,在苯并[a]芘(B[a]P)诱导的致癌模型中,通过饮食给予二甲双胍/吡格列酮可预防A/J小鼠肺腺瘤的形成,同时调节残留腺瘤中的化学预防和抗炎生物标志物。我们发现,与未治疗的对照组相比,在15周后,二甲双胍(500和850毫克/千克/天)和吡格列酮(15毫克/千克/天)作为单药治疗以及联合使用时,肺腺瘤的形成均有统计学意义的显著减少。单独使用二甲双胍以及与吡格列酮联合使用在早期和晚期干预时均导致肺腺瘤形成有统计学意义的显著减少。单独使用吡格列酮仅在早期治疗干预时导致腺瘤形成显著减少。我们得出结论,口服二甲双胍在500至1000毫克/千克/天的剂量范围内是一种可行的化学预防治疗方法。15毫克/千克/天的吡格列酮在早期干预时是一种可行的化学预防剂。二甲双胍和吡格列酮联合使用的效果与单独使用二甲双胍相当,且优于15毫克/千克/天的吡格列酮。由于这些药物已获得美国食品药品监督管理局(FDA)批准,因此有可能迅速开展人体临床研究。《癌症预防研究》;10(2);116 - 23。©2017美国癌症研究协会(AACR)