2'-Hydroxychalcone Induces Autophagy and Apoptosis in Breast Cancer Cells via the Inhibition of the NF-κB Signaling Pathway: In Vitro and In Vivo Studies

被引:3
|
作者
Wang, Xiao [1 ]
Liang, Yongjie [1 ]
Zhang, Bohan [1 ]
He, Lixin [1 ]
Li, Wenxuan [1 ]
Zhang, Wenwen [1 ]
Li, Chengzong [1 ]
Luo, Lihong [1 ]
Umar, Talha [1 ]
Feng, Huili [1 ,2 ]
Qiu, Changwei [1 ]
机构
[1] Huazhong Agr Univ, Coll Vet Med, Dept Clin Vet Med, Wuhan 430070, Peoples R China
[2] Coll Anim Husb Engn, Henan Vocat Coll Agr, Dept Anim Physiol & Mol Biol, Zhengzhou 451450, Peoples R China
基金
中国国家自然科学基金;
关键词
hydroxychalcone; autophagy; apoptosis; NF-kappa B signaling; reactive oxygen species; CYCLE PROGRESSION; UP-REGULATION; ACTIVATION; CHALCONE; EXPRESSION; BUTEIN; DEATH; ISOLIQUIRITIGENIN; INDUCTION; JNK;
D O I
10.3390/nu16040514
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
2'-Hydroxychalcone is a hydroxyl derivative of chalcones, which are biosynthetic precursors of flavonoids and rich in the human diet. The anticancer activity of 2'-hydroxychalcone has been reported in several cancers but remains to be investigated in breast cancer. In the current study, 2'-hydroxychalcone showed significant cytotoxicity against breast cancer cell lines MCF-7 and CMT-1211. It could inhibit breast cancer cell proliferation, migration, and invasion in vitro and suppress tumor growth and metastasis in vivo. Mechanistic investigation revealed that the NF-kappa B pathway was significantly inhibited by 2'-hydroxychalcone treatment accompanied by an excessive intracellular accumulation of reactive oxygen species, induction of endoplasmic reticulum stress, and activation of JNK/MAPK. In addition, 2'-hydroxychalcone elevated the autophagic levels in breast cancer cells equipped with increasing numbers of autophagy vesicles and complete autophagic flux. Finally, autophagy-dependent apoptosis was observed in 2'-hydroxychalcone-induced cell death. In conclusion, 2'-hydroxychalcone enhances the autophagic levels and induces apoptosis in breast cancer cells, which could be contributed to the inhibition of the pro-survival NF-kappa B signaling, indicating a promising potential for 2'-hydroxychalcone in future anticancer drug development.
引用
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页数:20
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