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β-Asarone Inhibits Invasion and EMT in Human Glioma U251 Cells by Suppressing Splicing Factor HnRNP A2/B1
by
Wang, Hongmei
, Yu, Zanyang
, Li, Li
, Wu, Mingxia
, Qi, Hongyi
, Xu, Xiaoyu
, Wang, Chengqiang
in
Anisoles - pharmacology
/ Antineoplastic Agents - pharmacology
/ Brain cancer
/ Brain Neoplasms - drug therapy
/ Brain Neoplasms - metabolism
/ brain tumor
/ Cell Adhesion - drug effects
/ Cell Line, Tumor
/ Cell Movement - drug effects
/ Cell Proliferation - drug effects
/ Cell Survival - drug effects
/ Cytotoxicity
/ Dose-Response Relationship, Drug
/ Down-Regulation
/ epithelial-mesenchymal transition
/ Epithelial-Mesenchymal Transition - drug effects
/ Gene Expression Regulation, Neoplastic - drug effects
/ Glioma
/ Glioma - drug therapy
/ Glioma - metabolism
/ Heterogeneous-Nuclear Ribonucleoproteins - antagonists & inhibitors
/ hnRNP A2/B1
/ Humans
/ Invasion
/ Investigations
/ Liver cancer
/ Lung cancer
/ Neoplasm Invasiveness
/ Nervous system
/ Pancreatic cancer
/ Proteins
/ Tumors
/ Wound healing
/ β-asarone
2018
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β-Asarone Inhibits Invasion and EMT in Human Glioma U251 Cells by Suppressing Splicing Factor HnRNP A2/B1
by
Wang, Hongmei
, Yu, Zanyang
, Li, Li
, Wu, Mingxia
, Qi, Hongyi
, Xu, Xiaoyu
, Wang, Chengqiang
in
Anisoles - pharmacology
/ Antineoplastic Agents - pharmacology
/ Brain cancer
/ Brain Neoplasms - drug therapy
/ Brain Neoplasms - metabolism
/ brain tumor
/ Cell Adhesion - drug effects
/ Cell Line, Tumor
/ Cell Movement - drug effects
/ Cell Proliferation - drug effects
/ Cell Survival - drug effects
/ Cytotoxicity
/ Dose-Response Relationship, Drug
/ Down-Regulation
/ epithelial-mesenchymal transition
/ Epithelial-Mesenchymal Transition - drug effects
/ Gene Expression Regulation, Neoplastic - drug effects
/ Glioma
/ Glioma - drug therapy
/ Glioma - metabolism
/ Heterogeneous-Nuclear Ribonucleoproteins - antagonists & inhibitors
/ hnRNP A2/B1
/ Humans
/ Invasion
/ Investigations
/ Liver cancer
/ Lung cancer
/ Neoplasm Invasiveness
/ Nervous system
/ Pancreatic cancer
/ Proteins
/ Tumors
/ Wound healing
/ β-asarone
2018
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β-Asarone Inhibits Invasion and EMT in Human Glioma U251 Cells by Suppressing Splicing Factor HnRNP A2/B1
by
Wang, Hongmei
, Yu, Zanyang
, Li, Li
, Wu, Mingxia
, Qi, Hongyi
, Xu, Xiaoyu
, Wang, Chengqiang
in
Anisoles - pharmacology
/ Antineoplastic Agents - pharmacology
/ Brain cancer
/ Brain Neoplasms - drug therapy
/ Brain Neoplasms - metabolism
/ brain tumor
/ Cell Adhesion - drug effects
/ Cell Line, Tumor
/ Cell Movement - drug effects
/ Cell Proliferation - drug effects
/ Cell Survival - drug effects
/ Cytotoxicity
/ Dose-Response Relationship, Drug
/ Down-Regulation
/ epithelial-mesenchymal transition
/ Epithelial-Mesenchymal Transition - drug effects
/ Gene Expression Regulation, Neoplastic - drug effects
/ Glioma
/ Glioma - drug therapy
/ Glioma - metabolism
/ Heterogeneous-Nuclear Ribonucleoproteins - antagonists & inhibitors
/ hnRNP A2/B1
/ Humans
/ Invasion
/ Investigations
/ Liver cancer
/ Lung cancer
/ Neoplasm Invasiveness
/ Nervous system
/ Pancreatic cancer
/ Proteins
/ Tumors
/ Wound healing
/ β-asarone
2018
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β-Asarone Inhibits Invasion and EMT in Human Glioma U251 Cells by Suppressing Splicing Factor HnRNP A2/B1
Journal Article
β-Asarone Inhibits Invasion and EMT in Human Glioma U251 Cells by Suppressing Splicing Factor HnRNP A2/B1
2018
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Overview
β-asarone, the main component in the volatile oil of Acori tatarinowii Rhizoma, has been found to possess antitumor activity. However, its effect and mechanisms against tumor invasion and epithelial–mesenchymal transition (EMT) are still unclear. In this study, no or less cytotoxicity was caused by β-asarone within 0–120 μM in human glioma U251 cells for 48 h. β-asarone (30 and 60 μM) inhibited the migration of U251 cells in the wound healing assay, suppressed the invasion of U251 cells in the Boyden chamber invasion assay, and inhibited the adhesion of U251 cells onto the Matrigel. Moreover, β-asarone suppressed EMT with the up-regulation of E-cadherin and the down-regulation of vimentin. HnRNP A2/B1, a well-characterized oncogenic protein, was shown at a high basal level in U251 cells and β-asarone reduced hnRNP A2/B1 expression in a concentration and time-dependent way. Importantly, hnRNP A2/B1 overexpression significantly counteracted the inhibition of β-asarone on the migration, invasion, and adhesion of U251 cells and reversed the modulation of EMT markers by β-asarone. Additionally, β-asarone decreased the MMP-9 and p-STAT3 in U251 cells, which was also reversed by hnRNP A2/B1 overexpression. Together, our results suggest that hnRNP A2/B1 may be a potential molecular target underlying the inhibitory effect of β-asarone on invasion and EMT in glioma cells.
Publisher
MDPI AG,MDPI
Subject
/ Antineoplastic Agents - pharmacology
/ Brain Neoplasms - drug therapy
/ Brain Neoplasms - metabolism
/ Cell Adhesion - drug effects
/ Cell Movement - drug effects
/ Cell Proliferation - drug effects
/ Cell Survival - drug effects
/ Dose-Response Relationship, Drug
/ epithelial-mesenchymal transition
/ Epithelial-Mesenchymal Transition - drug effects
/ Gene Expression Regulation, Neoplastic - drug effects
/ Glioma
/ Heterogeneous-Nuclear Ribonucleoproteins - antagonists & inhibitors
/ Humans
/ Invasion
/ Proteins
/ Tumors
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