Protective Effect of Metformin in an Aberrant Crypt Foci Model Induced by 1,2-Dimethylhydrazine: Modulation of Oxidative Stress and Inflammatory Process

被引:20
|
作者
Bordini, Heloiza Paranzini [1 ]
Kremer, Jean Lucas [1 ]
Fagundes, Tatiane Renata [1 ]
Melo, Gabriella Pasqual [2 ]
Conchon-Costa, Ivete [3 ]
da Silva, Suelen Santos [3 ]
Cecchini, Alessandra Lourenco [2 ]
Panis, Carolina [4 ]
Luiz, Rodrigo Cabral [1 ]
机构
[1] Univ Estadual Londrina, Dept Pathol Sci, Lab Mol Pathol, Londrina, Brazil
[2] Univ Estadual Londrina, Dept Pathol Sci, Lab Pathophysiol Free Radicals, Londrina, Brazil
[3] State Univ, Dept Pathol Sci, Parasitol Lab, Londrina, Brazil
[4] State Univ West Parana, Ctr Healthy Sci, Lab Inflammatory Mediators, Francisco Beltrao, Brazil
关键词
colorectal cancer; metformin; 1,2-dimethylhydrazine; aberrant crypt foci; prevention; APOPTOTIC CELL-DEATH; NITRIC-OXIDE; COLON CARCINOGENESIS; CANCER; EXPRESSION; ACID; PROLIFERATION; ACTIVATION;
D O I
10.1002/mc.22545
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Colorectal Cancer (CRC) is the third most frequent type of cancer worldwide. In the past few years, studies have revealed a protective effect of metformin (METan anti-hyperglycemic drug, used to treat type 2 diabetes), against CRC. The protective effect of MET has been associated with AMPK activation (and mTOR inhibition), resulting in suppressed protein synthesis, and reduced cell proliferation in malignant transformed cells. To elucidate new mechanisms for the protective effect of metformin, we evaluated the oxidative stress and inflammatory process modulation, since these processes are strictly involved in colorectal carcinogenesis. The present study evaluated the protective effect of MET in a CRC model induced by 1,2-dimethylhydrazine (DMH) in Balb/c female mice. The simultaneous/continuous treatment (administration of MET and DMH simultaneously), revealed protective activity of MET, preventing the formation of aberrant crypt foci (ACF) in 71.4% at distal colon sections, and was able to restore basal labeling of apoptosis. Treatment with MET also reduced the inflammatory process induced by DMH, resulting in of the reduction of oxidative stress and nitric oxide related parameters. (C) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:913 / 922
页数:10
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