Protective Effects of [6]-Paradol on Histological Lesions and Immunohistochemical Gene Expression in DMBA Induced Hamster Buccal Pouch Carcinogenesis

被引:20
|
作者
Mariadoss, Arokia Vijayaanand [1 ]
Kathiresan, Suresh [1 ]
Muthusamy, Rajasekar [1 ]
Kathiresan, Sivakumar [2 ]
机构
[1] Annamalai Univ, Fac Sci, Dept Biochem & Biotechnol, Annamalainagar 608002, Tamil Nadu, India
[2] Annamalai Univ, Fac Sci, Dept Bot, Annamalainagar 608002, Tamil Nadu, India
关键词
6]-paradol; apoptosis; DMBA; hamster; oral squamous cell carcinoma; P53; APOPTOSIS; ACTIVATION; INDUCTION; GINGER; FAMILY; DEATH; HEAD; BAX;
D O I
10.7314/APJCP.2013.14.5.3123
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The search for naturally occurring agents in routinely consumed foods that may inhibit cancer development is of high priority. [6]-Paradol is a pungent phenolic bioactive component from ginger with well-documented health promoting antioxidant, antimutagenic, antigenotoxic and anti-inflammatory properties. However, anticarcinogenic effects have yet to be fully explored. The objectives of the present study were therefore to assess protective effects against 7,12-dimethylbenz(a)anthracene (DMBA) induced buccal pouch carcinogenesis in male golden Syrian hamsters. Methods: Oral squamous cell carcinomas developed in the left buccal pouch of hamsters on painting with 0.5% of DMBA, three times in a week. To assess the apoptotic associated gene expressing potential of [6]-paradol, it was orally administered to DMBA treated hamsters on alternate days from DMBA painting for 14 weeks. Results: We observed 100% tumor formation with marked levels of neoplastic changes and altered the expression of apoptotic associated gene (p53, bcl-2, caspase-3 and TNF-alpha) was observed in the DMBA alone painted hamsters as compared to control hamsters. Oral administration of [6]-paradol at a dose of 30 mg/kg b.wt to DMBA treated animals on alternative days for 14 weeks significantly reduced the neoplastic changes and improved the status of apoptosis associated gene expression. Conclusion: These observations confirmed that [6]-paradol acts as a tumor suppressing agent against DMBA induced oral carcinogenesis. We also conclude that [6]-paradol also effectively enhances apoptosis-associated gene expression in DMBA treated animals.
引用
收藏
页码:3123 / 3129
页数:7
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