Hyperoside and let-7a-5p synergistically inhibits lung cancer cell proliferation via inducing G1/S phase arrest

被引:38
作者
Li, Jia-Peng [1 ]
Liao, Xing-Hua [1 ]
Xiang, Yuan [1 ]
Yao, Ao [1 ]
Song, Ru-Hui [1 ]
Zhang, Zi-Jian [1 ]
Huang, Feng [1 ]
Dai, Zhou-Tong [1 ]
Zhang, Tong-Cun [1 ,2 ]
机构
[1] Wuhan Univ Sci & Technol, Coll Life & Hlth Sci, Inst Biol & Med, Wuhan 430081, Hubei, Peoples R China
[2] Tianjin Univ Sci & Technol, Coll Biotechnol, Key Lab Ind Fermentat Microbiol, Minist Educ & Tianjin, Tianjin 300457, Peoples R China
基金
中国国家自然科学基金;
关键词
Lung cancer; Hyperoside; Proliferation; Let-7a-5p; CCND1; IN-VITRO; MICRORNA; INFLAMMATION; APOPTOSIS;
D O I
10.1016/j.gene.2018.09.011
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Lung cancer remains one of the most aggressive human malignancies with a low survival rate. Hyperoside (quercetin 3-O-beta-D-galactopyranoside) is a flavonol glycoside with an anti-cancer activity. The microRNA-let-7 was widely regarded as a tumor suppressor in human tumors. Here, we investigated the role of hyperoside and let-7a-5p on the lung cancer cell proliferation, cell cycle and apoptosis in A549 cells in vitro. Our results showed that hyperoside could inhibit the proliferation of A549 cells through inducing apoptosis and G1/S phase arrest. Let-7a-5p could inhibit the proliferation of A549 cells via inhibiting the process of G1/S phase. Additionally, hyperoside and let-7a-5p had a synergetic effect on suppressing the proliferation of A549 cells; microRNA-let-7a-5p directly regulated the expression of CCND1 in A549 cells. Our study illustrated that hyperoside and microRNA-let7a-5p might provide a synergistic effect on anti-cancer, which may provide a new idea for lung cancer treatment.
引用
收藏
页码:232 / 240
页数:9
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