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Inhibition of β-catenin and KRAS Expressions by Piper betle in Azoxymethane-induced Colon Cancer of Male Fischer 344 Rats
被引:0
|作者:
Esa, Faezah
[1
]
Ngah, Wan Zurinah Wan
[1
,2
]
Jamal, A. Rahman A.
[2
]
Yusof, Yasmin Anum Mohd
[1
]
机构:
[1] Univ Kebangsaan Malaysia, Fac Med, Dept Biochem, Kuala Lumpur 50300, Malaysia
[2] Univ Kebangsaan Malaysia, Med Ctr, Inst Mol Biol, Cheras, Malaysia
来源:
ANALYTICAL AND QUANTITATIVE CYTOLOGY AND HISTOLOGY
|
2013年
/
35卷
/
06期
关键词:
azoxymethane;
beta-catenin;
chemoprevention;
chemoprophylaxis;
colon cancer;
Ki-ras protein;
rat;
Piper betle;
sarcospan (Kras oncogene-associated gene) protein;
human;
ABERRANT CRYPT FOCI;
COLORECTAL-CANCER;
CARCINOGENESIS;
CHEMOPREVENTION;
P53;
PLANT;
P21;
ANTIOXIDANT;
MECHANISMS;
QUERCETIN;
D O I:
暂无
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
OBJECTIVE: To investigate the chemopreventive effect of Piper betle (PB) on preneoplastic lesions (aberrant crypt foci [ACF] induced by azoxymethane (AOM) in rats and its effect on colorectal cancer biomarkers (beta-catenin, KRAS, p53 and p21). STUDY DESIGN: A total of 32 male Fischer 344 rats were divided into phase 1 and phase 2 groups (8 and 24 weeks of AOM administration, respectively). Each phase was divided into 4 groups: control or normal saline (NS) (1 mL/kg), AOM (15 mg/kg body weight, once weekly for 2 weeks), PB (75 mg/kg body weight) and AOM + PB. PB was force-fed to rats a week after the second dose of AOM and NS. The colon was cut open longitudinally for methylene blue and immunohistochemistry staining. RESULTS: AOM administration showed formation of ACF at 8 and 24 weeks. PB, however, did not reduce ACF formation at either week, but it managed to reduce beta-catenin expression and KRAS found highly expressed in the AOM group of phase 1 rats. No immunoreactivities of p53 and p21 were detected in phase 2 rats, but instead inflammatory cells were visible in between the lesions. CONCLUSION: PB may act as a potential chemopreventive agent in the early stage of colon carcinogenesis by suppressing the expressions of beta-catenin and KRAS.
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页码:324 / 334
页数:11
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