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1.
Drug Dev Res ; 83(2): 432-446, 2022 04.
Artigo em Inglês | MEDLINE | ID: mdl-34636432

RESUMO

Paeonol exerted an effect in lung cancer, but the underlying mechanism remained vague. In this research, we assessed the effects of Paeonol and microRNA (miR)-126-5p on the viability, migration, invasion, and epithelial-mesenchymal transition (EMT) of lung cancer cells. Lung cancer cells and BEAS-2B cells were treated with Paeonol, and viability was detected by 3-(4,5)-dimethylthiahiazo (-z-y1)-3,5-di- phenytetrazoliumromide (MTT) assay. The migration and invasion of lung cancer cells after treatment with Paeonol at 40 µg/mL or 80 µg/mL were detected by wound healing assay and Transwell assay, respectively. The effects of Paeonol on transforming growth factor-ß1 (TGF-ß1)-induced EMT and relative expressions of EMT-related proteins were determined using Western blot. The target gene of miR-126-5p and the binding sites between them were predicted by TargetScan, and confirmed using dual-luciferase reporter assay. Relative expressions of miR-126-5p, its target gene and EMT-related proteins were determined by quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot. Rescue assay was performed to analyze the relation between Paeonol and miR-126-5p. Paeonol down-regulated cell viability and inhibited migration, invasion and TGF-ß1-induced EMT while up-regulating miR-126-5p expression in lung cancer cells as the dose increased. However, miR-126-5p inhibitor could reverse the effect of Paeonol. ZEB2 was the target gene of miR-126-5p, and silencing ZEB2 expression reversed the effects of miR-126-5p downregulation. Paeonol also regulated the expression of ZEB2 in lung cancer cells, and this regulation depends on the regulation of miR-126-5p. Paeonol inhibits human lung cancer cell viability and metastasis via the miR-126-5p/ZEB2 axis, and could be adopted as a potential agent for lung cancer treatment.


Assuntos
Neoplasias Pulmonares , MicroRNAs , Acetofenonas , Linhagem Celular Tumoral , Movimento Celular , Proliferação de Células , Sobrevivência Celular , Regulação Neoplásica da Expressão Gênica , Humanos , Neoplasias Pulmonares/tratamento farmacológico , Neoplasias Pulmonares/genética , MicroRNAs/genética , MicroRNAs/metabolismo , Invasividade Neoplásica/genética , Invasividade Neoplásica/patologia , Fator de Crescimento Transformador beta1/metabolismo , Homeobox 2 de Ligação a E-box com Dedos de Zinco/genética , Homeobox 2 de Ligação a E-box com Dedos de Zinco/metabolismo
2.
IEEE Sens J ; 17(11): 3323-3331, 2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-31467492

RESUMO

We present a radio-frequency (RF) sensor and its measurement results of three volatile organic compounds (VOCs) at multiple frequency points from ∼ 2 to ∼ 11 GHz, which is a convenient range in our examination. The sensor is based on a simple RF interferometer and uses two coplanar waveguides (CPWs), A and B of 5 and 25 mm length, respectively, as VOC sensing electrodes. Approximately 70-nm-thick poly copolymer films are coated on CPW surfaces for VOC adsorption and concentration. It is shown that ethanol, acetone, and isopropyl (IPA) induce frequency-dependent RF responses, which are also VOC-dependent. Thus, the frequency-dependent properties provide a possible new approach for better VOC sensing selectivity. With CPW A, the limit-of-detections (LODs) are ∼ 600 ppm for ethanol, ∼ 270 ppm for acetone, and ∼ 330 ppm for IPA at 9.29 GHz. With CPW B, the LODs are roughly four times better. These LODs are also better than most of other RF VOC sensor results. In the future work, it is promising to further improve RF sensitivity and selectivity significantly.

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