Heme oxygenase-1 has antitumoral effects in colorectal cancer: Involvement of p53

被引:43
作者
Carolina Andres, Nancy [1 ]
Eugenia Fermento, Maria [1 ]
Ariel Gandini, Norberto [1 ]
Lopez Romero, Alejandro [2 ]
Ferro, Alejandro [3 ]
Gonzalez Donna, Lucila [3 ]
Carlos Curino, Alejandro [1 ]
Marta Facchinetti, Maria [1 ]
机构
[1] Ctr Cient Tecnol INIBIBB CCT CONICET, Inst Invest Bioquim Bahia Blanca, Lab Biol Canc, Bahia Blanca, Buenos Aires, Argentina
[2] IACA Labs, Bahia Blanca, Buenos Aires, Argentina
[3] Hosp Italiano Reg, Serv Oncol, Bahia Blanca, Buenos Aires, Argentina
关键词
Heme oxygenase-1; Colorectal cancer; P53; Survival; Immunohistochemistry; PROTEIN-KINASE-C; NUCLEAR TRANSLOCATION; NITRIC-OXIDE; EXPRESSION; CELLS; SURVIVAL; COLON; GROWTH; OVEREXPRESSION; ACTIVATION;
D O I
10.1016/j.yexmp.2014.09.012
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The expression of heme oxygenase-1 (HO-1) has been shown to be up-regulated in colorectal cancer (CRC), but the role it plays in this cancer type has not yet been addressed. The aims of this study have been to analyze HO-1 expression in human invasive CRC, evaluate its correlation with clinical and histo-pathological parameters and to investigate the mechanisms through which the enzyme influences tumor progression. We confirmed that HO-1 was over-expressed in human invasive CRC and found that the expression of the enzyme was associated with a longer overall survival time. In addition, we observed in a chemically-induced CRC animal model that total and nuclear HO-1 expression increases with tumor progression. Our investigation of the mechanisms involved in HO-1 action in CRC demonstrates that the protein reduces cell viability through induction of cell cycle arrest and apoptosis and, importantly, that a functional p53 tumor suppressor protein is required for these effects. This reduction in cell viability is accompanied by modulation of the levels of p21, p27, and cyclin D1 and by modulation of Akt and PKC pathways. Altogether, our results demonstrate an antitumoral role of HO-1 and points to the importance of p53 status in this antitumor activity. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:321 / 331
页数:11
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