Journal of Receptors and Signal Transduction · 2020 · 26 citations · 22 references
MedicineOncologyPharmacologyCancer PharmacologyMolecular OncologyNeoplasiaCancer Cell SignalingCell Signaling DisruptionCellular Responses To HypoxiaCervical CancerHypoxia AdaptationOncogenic Signaling PathwaysEpithelial-mesenchymal Transition In HypoxiaEpithelial-mesenchymal Transition MarkersHypoxia-driven InvasionHypoxia-induced EmtHypoxic MicroenvironmentPhosphatidylinositol 3-Kinase-akt PathwayPi3k-akt Signaling PathwayTumor Cell Invasion Under Hypoxia
Plantamajoside (PMS) is a major compound of Plantago asiatica and possesses anti-tumor property in several types of cancers. However, the effect of PMS on cervical cancer has not been investigated. This study aimed to investigate the effect of PMS on the migration and invasion of cervical cancer cell lines under hypoxic condition. Our results demonstrated that PMS significantly inhibited hypoxia-caused increases in cell migration and invasion of cervical cancer cells. The hypoxia-induced epithelial-mesenchymal transition (EMT) process was prevented by PMS with increased E-cadherin expression, and decreased expression levels of N-cadherin and vimentin in cervical cancer cells. Besides, the expression levels of transcription factors slug and snail were suppressed by PMS in hypoxia-induced cervical cancer cells. The increased mRNA and protein levels of hypoxia-inducible factor 1alpha (HIF-1α) in hypoxia-induced cervical cancer cells were prevented by PMS. Furthermore, PMS blocked the hypoxia-induced activation of NF-κB and PI3K/Akt pathway in cervical cancer cells. Taken together, these findings suggest that PMS exerted an anti-tumor activity in cervical cancer through preventing the hypoxia-induced EMT. Thus, PMS might serve as a therapeutic agent for the treatment of cervical cancer.
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Christina Befani, Panagiotis J. Vlachostergios, Eleana Hatzidaki et al. · Journal of Molecular Medicine · 2011 · 133 citations
Junko Yoshida, Akiko Horiuchi, Norihiko Kikuchi et al. · Medical Molecular Morphology · 2009 · 102 citations
Medicine, Cancer Biology, Oncology +17