Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10143484 | Gene | 2018 | 9 Pages |
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.
Keywords
5′untranslated regionRIPAMUTATCCMNCCyclin D1qRT-PCRRT-PCRGAPDHCDK4CCND1PVDFRadioimmune precipitation assayCCK-8negative controlsPBSRNase3′untranslated region3′UTR5′UTR5-ethynyl-2′-deoxyuridineCdk6DMSOEdUquantitative real-time RT-PCRRNAribonucleic acidsodium dodecyl sulphate-polyacrylamide gel electrophoresisSDS-PAGESCLCTwo-way analysis of varianceANOVAProliferationcoding sequencestandard error of the meanDimethyl sulfoxideribonucleaseLung cancerNon-small-cell lung cancerSmall-cell lung cancerNSCLCcyclin-dependent kinase 6American Type Culture CollectionPhosphate-buffered salineSEMMicroRNAMiRNAmutant typewild typeHyperosideIncreverse-transcription polymerase chain reactionWestern blotPolyvinylidene fluorideCdScyclin-dependent kinase 4glyceraldehyde 3-phosphate dehydrogenase
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Genetics
Authors
Jia-Peng Li, Xing-Hua Liao, Yuan Xiang, Ao Yao, Ru-Hui Song, Zi-Jian Zhang, Feng Huang, Zhou-Tong Dai, Tong-Cun Zhang,