The Protective Effect of Sanggenol L Against DMBA-induced Hamster Buccal Pouch Carcinogenesis Induces Apoptosis and Inhibits Cell Proliferative Signalling Pathway

被引:4
作者
Fu, Qing [1 ]
Zhang, Fangming [2 ]
Vijayalakshmi, Annamalai [3 ]
机构
[1] Peoples Hosp Qijiang Dist, Dept Stomatol, Chongqing 401420, Peoples R China
[2] Fifth Peoples Hosp Wuxi, Dept Stomatol, Wuxi 214000, Peoples R China
[3] Rabiammal Ahamed Maideen Coll Women, Dept Biochem, Thiruvarur 610001, Tamil Nadu, India
关键词
Oral cancer; sanggenol L; DMBA; apoptosis; cell proliferation; OSCC; NF-KAPPA-B; ANTICANCER AGENTS; MEDICINAL-PLANTS; ORAL-CANCER; ANTIOXIDANTS; EPIDEMIOLOGY; ASSAY;
D O I
10.2174/1386207326666230726140706
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Oral squamous cell carcinoma (OSCC) has a poor prognosis when treated with surgery and chemotherapy. Therefore, a new therapy and preventative strategy for OSCC and its underlying mechanisms are desperately needed. The purpose of this study was to examine the chemopreventive effects of sanggenol L on oral squamous cell carcinoma (OSCC). The research focused on molecular signalling pathways in 7,12-dimethylbenz(a)anthracene (DMBA)-induced hamster buccal pouch (HBP) carcinogenesis.Aim: The purpose of this study was to look at the biochemical and chemopreventive effects of sanggenol L on 7,12-dimethylbenz(a)anthracene (DMBA)-induced HBP (hamster buccal pouch) carcinogenesis via cell proliferation and the apoptotic pathway.Methods: After developing squamous cell carcinoma, oral tumours continued to progress leftward into the pouch 3 times per week for 10 weeks while being exposed to 0.5% reactive DMBA three times per week. Tumour growth was caused by biochemical abnormalities that induced inflammation, increased cell proliferation, and decreased apoptosis.Results: Oral sanggenol L (10 mg/kg bw) supplementation with cancer-induced model DMBA-painted hamsters prevented tumour occurrences, improved biochemistry, inhibited inflammatory markers, decreased cell proliferation marker expression of tumour necrosis factor-alpha (TNF- alpha), nuclear factor (NF-kappa B), cyclooxygenase-2 (COX-2), inducible nitric oxide synthase (iNOS), and induced apoptosis.Conclusion: Sanggenol L could be developed into a new medicine for the treatment of oral carcinogenesis.
引用
收藏
页码:885 / 893
页数:9
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