| Literature DB >> 30201337 |
Jia-Peng Li1, Xing-Hua Liao2, Yuan Xiang1, Ao Yao1, Ru-Hui Song1, Zi-Jian Zhang1, Feng Huang1, Zhou-Tong Dai1, Tong-Cun Zhang3.
Abstract
Lung cancer remains one of the most aggressive human malignancies with a low survival rate. Hyperoside (quercetin-3-O-β-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.Entities:
Keywords: CCND1; Hyperoside; Let-7a-5p; Lung cancer; Proliferation
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Year: 2018 PMID: 30201337 DOI: 10.1016/j.gene.2018.09.011
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688