Fixed-Dose Combinations of Pioglitazone and Metformin for Lung Cancer Prevention

被引:24
|
作者
Seabloom, Donna E. [1 ,2 ]
Galbraith, Arthur R. [1 ]
Haynes, Anna M. [1 ,2 ]
Antonides, Jennifer D. [1 ]
Wuertz, Beverly R. [1 ,2 ,3 ]
Miller, Wendy A. [3 ]
Miller, Kimberly A. [3 ]
Steele, Vernon E. [4 ]
Miller, Mark Steven [4 ]
Clapper, Margie L. [5 ]
O'Sullivan, M. Gerard [6 ]
Ondrey, Frank G. [1 ,2 ,3 ]
机构
[1] Univ Minnesota, Masonic Canc Ctr, Minneapolis, MN USA
[2] Univ Minnesota, Coll Pharm, AeroCore Inhalat Testing, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Otolaryngol, Minneapolis, MN USA
[4] NCI, Div Canc Prevent, Rockville, MD USA
[5] Fox Chase Canc Ctr, Philadelphia, PA USA
[6] Univ Minnesota, Masonic Canc Ctr, Comparat Pathol, Minneapolis, MN USA
关键词
ACTIVATED RECEPTOR-GAMMA; FACTOR-KAPPA-B; MALE F344 RATS; DIABETIC-PATIENTS; BRONCHIAL EPITHELIUM; CALORIE RESTRICTION; ENDOTHELIAL-CELLS; GROWTH-INHIBITION; CARCINOMA CELLS; TUMOR-INCIDENCE;
D O I
10.1158/1940-6207.CAPR-16-0232
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 singleagent 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 earlystage interventions. Combination metformin and pioglitazone performed equal to metformin alone and better than pioglitazone at 15 mg/kg/d. Because the drugs are already FDAapproved, rapid movement to human clinical studies is possible.
引用
收藏
页码:116 / 123
页数:8
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