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
相关论文
共 49 条
[1]   Epidemiology of oral cancer in Arab countries [J].
Al-Jaber, Abeer ;
Al-Nasser, Lubna ;
El-Metwally, Ashraf .
SAUDI MEDICAL JOURNAL, 2016, 37 (03) :249-255
[2]   Anticancer and antioxidant profiling effects of Nerolidol against DMBA induced oral experimental carcinogenesis [J].
Balakrishnan, Vaitheeswari ;
Ganapathy, Sindhu ;
Veerasamy, Vinothkumar ;
Duraisamy, Ramachandhiran ;
Sathiavakoo, Vigil Anbiah ;
Krishnamoorthy, Vasudevan ;
Lakshmanan, Vennila .
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2022, 36 (06)
[3]  
BEUTLER E, 1963, J LAB CLIN MED, V61, P882
[4]   Medicinal plants and cancer chemoprevention [J].
Desai, Avni G. ;
Qazi, Ghulam N. ;
Ganju, Ramesh K. ;
El-Tamer, Mahmoud ;
Singh, Jaswant ;
Saxena, Ajit K. ;
Bedi, Yashbir S. ;
Taneja, Subhash C. ;
Bhat, Hari K. .
CURRENT DRUG METABOLISM, 2008, 9 (07) :581-591
[5]  
DESAI ID, 1984, METHOD ENZYMOL, V105, P138, DOI 10.1016/S0076-6879(84)05019-9
[6]   Target-based anticancer indole derivatives and insight into structure-activity relationship: A mechanistic review update (2018-2021) [J].
Dhiman, Ashima ;
Sharma, Rupam ;
Singh, Rajesh K. .
ACTA PHARMACEUTICA SINICA B, 2022, 12 (07) :3006-3027
[7]   Extracellular Reactive Oxygen Species Drive Apoptosis-Induced Proliferation via Drosophila Macrophages [J].
Fogarty, Caitlin E. ;
Diwanji, Neha ;
Lindblad, Jillian L. ;
Tare, Meghana ;
Amcheslavsky, Alla ;
Makhijani, Kalpana ;
Brueckner, Katja ;
Fan, Yun ;
Bergmann, Andreas .
CURRENT BIOLOGY, 2016, 26 (05) :575-584
[8]   Reactive oxygen species and cancer paradox: To promote or to suppress? [J].
Galadari, Sehamuddin ;
Rahman, Anees ;
Pallichankandy, Siraj ;
Thayyullathil, Faisal .
FREE RADICAL BIOLOGY AND MEDICINE, 2017, 104 :144-164
[9]   DENTITION, DIET, TOBACCO, AND ALCOHOL IN EPIDEMIOLOGY OF ORAL CANCER [J].
GRAHAM, S ;
DAYAL, H ;
ROHRER, T ;
SWANSON, M ;
SULTZ, H ;
SHEDD, D ;
FISCHMAN, S .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1977, 59 (06) :1611-1618
[10]   The COX-2/PGE2 pathway: key roles in the hallmarks of cancer and adaptation to the tumour microenvironment [J].
Greenhough, Alexander ;
Smartt, Helena J. M. ;
Moore, Amy E. ;
Roberts, Heather R. ;
Williams, Ann C. ;
Paraskeva, Christos ;
Kaidi, Abderrahmane .
CARCINOGENESIS, 2009, 30 (03) :377-386