Cellular mechanisms mediating the anti-cancer effects of carnosol on gingiva carcinoma

被引:3
|
作者
Gassib, Nassima [1 ]
Issa, Hawraa [1 ]
Loubaki, Lionel [2 ]
Behaz, Sarah [1 ]
Almutairi, Mikhlid H. [3 ]
Rouabhia, Mahmoud [1 ]
Semlali, Abdelhabib [1 ]
机构
[1] Univ Laval, Fac Med Dentaire, Grp Rech Ecol buccale, Quebec City, PQ G1V 0A6, Canada
[2] Hema Quebec, 1070 Ave Sci De La Vie, Quebec City, PQ G1V 5C3, Canada
[3] King Saud Univ, Coll Sci, Zool Dept, POB 2455, Riyadh 11451, Saudi Arabia
来源
SCIENTIFIC REPORTS | 2024年 / 14卷 / 01期
关键词
Carnosol; Oral cancer; Gingiva carcinoma; Cell cycle; A poptosis; Oxidative stress; Migration; Signaling pathways; PROSTATE-CANCER; DIETARY DITERPENE; CYCLE ARREST; ANTIOXIDANT; EXPRESSION; SURVIVIN; APOPTOSIS; BRCA1; TRANSCRIPTION; LOCALIZATION;
D O I
10.1038/s41598-024-60797-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Carnosol, a rosemary polyphenol, displays anticancer properties and is suggested as a safer alternative to conventional surgery, radiotherapy, and chemotherapy. Given that its effects on gingiva carcinoma have not yet been investigated, the aim of this study was to explore its anti-tumor selectivity and to unravel its underlying mechanisms of action. Hence, oral tongue and gingiva carcinoma cell lines exposed to carnosol were analyzed to estimate cytotoxicity, cell viability, cell proliferation, and colony formation potential as compared with those of normal cells. Key cell cycle and apoptotic markers were also measured. Finally, cell migration, oxidative stress, and crucial cell signaling pathways were assessed. Selective anti-gingiva carcinoma activity was disclosed. Overall, carnosol mediated colony formation and proliferation suppression in addition to cytotoxicity induction. Cell cycle arrest was highlighted by the disruption of the c-myc oncogene/p53 tumor suppressor balance. Carnosol also increased apoptosis, oxidative stress, and antioxidant activity. On a larger scale, the alteration of cell cycle and apoptotic profiles was also demonstrated by QPCR array. This was most likely achieved by controlling the STAT5, ERK1/2, p38, and NF-& kgreen;B signaling pathways. Lastly, carnosol reduced inflammation and invasion ability by modulating IL-6 and MMP9/TIMP-1 axes. This study establishes a robust foundation, urging extensive inquiry both in vivo and in clinical settings, to substantiate the efficacy of carnosol in managing gingiva carcinoma.
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页数:16
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