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Teadenol B as a Component of Microorganism-Fermented Tea Extract Inhibited Breast Cancers by Promoting Autophagy.
Zhao, Ying; Ding, Zhang-Gui; Yan, Yu-Jie; Yang, Rui; Qi, Miao-Miao; Pan, Shu-Kang; Xie, Ji-Ling; Sun, Yu-Hui; Xiang, Jin.
Afiliação
  • Zhao Y; Ministry of Education Laboratory of Combinatorial Biosynthesis and Drug Discovery, School of Pharmaceutical Science, Wuhan University, Wuhan 430071, China.
  • Ding ZG; Pu-erh Tea Fermentation Engineering Research Center of Yunnan Province, Kunming 650271, China.
  • Yan YJ; Key Laboratory of Pu-erh Tea Processing Technology, Ministry of Agriculture and Rural Affairs, Kunming 650271, China.
  • Yang R; Yunnan Dayi Microbial Technology Co., Ltd., Kunming 650271, China.
  • Qi MM; Yunnan Institute of Microbiology, School of Life Sciences, Yunnan University, Kunming 650091, China.
  • Pan SK; Key Laboratory for Southwest Microbial Diversity of the Ministry of Education, Yunnan University, Kunming 650091, China.
  • Xie JL; Ministry of Education Laboratory of Combinatorial Biosynthesis and Drug Discovery, School of Pharmaceutical Science, Wuhan University, Wuhan 430071, China.
  • Sun YH; Pu-erh Tea Fermentation Engineering Research Center of Yunnan Province, Kunming 650271, China.
  • Xiang J; Key Laboratory of Pu-erh Tea Processing Technology, Ministry of Agriculture and Rural Affairs, Kunming 650271, China.
Molecules ; 29(4)2024 Feb 16.
Article em En | MEDLINE | ID: mdl-38398624
ABSTRACT
Breast cancer is a significant threat to life and health, which needs more safe and effective drugs to be explored. Teadenol B is a characteristic chemical component of microbial fermented tea. This study discovered that teadenol B could exhibit obvious inhibitory effects on all four different clinical subtype characteristics of breast cancer cells. Proteomic studies show that deoxycytidine triphosphate deaminase (DCTD), which could block DNA synthesis and repair DNA damage, had the most significant and consistent reduction in all four types of breast cancer cells with the treatment of teadenol B. Considering MDA-MB-231 cells exhibit poor clinical prognosis and displayed substantial statistical differences in KEGG pathway enrichment analysis results, we investigated its impact on the size and growth of MDA-MB-231 triple-negative breast tumors transplanted into nude mice and demonstrated that teadenol B significantly suppressed tumor growth without affecting body weight significantly. Finally, we found that the conversion of LC3-I to LC3-II in MDA-MB-231 increased significantly with teadenol B treatment. This proved that teadenol B could be a strong autophagy promotor, which explained the down-regulation of DCTD to some extent and may be the potential mechanism underlying teadenol B's anti-breast cancer effects. This finding provides new evidence for drinking fermented tea to prevent breast cancer and highlights the potential of teadenol B as a novel therapeutic option for breast cancer prevention and treatment, necessitating further investigations to clarify its exact target and the details involved.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apoptose / Neoplasias de Mama Triplo Negativas Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Apoptose / Neoplasias de Mama Triplo Negativas Idioma: En Ano de publicação: 2024 Tipo de documento: Article