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Qingxi Yue

Researcher at Chinese Academy of Sciences

Publications -  5
Citations -  122

Qingxi Yue is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Medicine & CYP3A4. The author has an hindex of 3, co-authored 3 publications receiving 88 citations.

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Pungent ginger components modulates human cytochrome P450 enzymes in vitro

TL;DR: 6-, 8-, and 10-gingerol suppress human cytochrome P450 activity, while 8- and10-gingers inhibit CYP3A4 expression, which may have an implication for the use of ginger or ginger products when combined with therapeutic drugs that are metabolized by cyto Chrome P450 enzymes.
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Dihydroartemisinin selectively inhibits PDGFRα-positive ovarian cancer growth and metastasis through inducing degradation of PDGFRα protein.

TL;DR: Dihydroartemisinin, one of the most active derivatives of ArtemisinIn, directly targets platelet-derived growth factor receptor-alpha (PDGFRα) to inhibit ovarian cancer cell growth and metastasis and shed high light on future development of novel Artemisinin-based targeted therapy.
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Artemisinin rewires the protein interaction network in cancer cells: network analysis, pathway identification, and target prediction

TL;DR: An analysis based on biological networks provides a deeper understanding of the molecular mechanisms of action of artemisinins and will contribute to the development and application of this class of compounds in cancer treatment.
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Ejiao ameliorates lipopolysaccharide-induced pulmonary inflammation via inhibition of NFκB regulating NLRP3 inflammasome and mitochondrial ROS.

TL;DR: Wang et al. as discussed by the authors showed Ejiao had a protective effect against LPS-elicited inflammatory lung epithelial Beas 2B cells (LILEB 2B).
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Amygdalin Induced Mitochondria-Mediated Apoptosis of Lung Cancer Cells via Regulating NF[Formula: see text]B-1/NF[Formula: see text]B Signaling Cascade in Vitro and in Vivo.

TL;DR: Amygdalin might be a potential activator of NF, which sheds more light on the molecular mechanism of anticancer effects of amygdalin, which warrants its development as a therapy for lung cancer.