<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wu GJ</submitter><funding>Health and Welfare Surcharge of Tobacco Products</funding><funding>Shin Kong Wu Ho-Su Memorial Hospital</funding><pagination>667-672</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5067977</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9</volume><pubmed_abstract>This article contains raw and processed data related to a research, "Honokiol induces autophagic cell death in malignant glioma through reactive oxygen species-mediated regulation of the p53/PI3K/Akt/mTOR signaling pathway" (C.J. Lin, T.L. Chen, Y.Y. Tseng, G.J. Wu, M.H. Hsieh, Y.W. Lin, R.M. Chen, 2016) [1]. Data were obtained by immunoblotting analyses of light chain 3 (LC3)-II, beclin-1, Akt, and mTOR in human glioma U87 MG cells and mouse glioma tissues treated with honokiol, an active constituent extracted from the bark of &lt;i>Magnolia officinalis, "&lt;/i>Honokiol induces autophagy of neuroblastoma cells through activating the PI3K/Akt/mTOR and endoplasmic reticular stress/ERK1/2 signaling pathways and suppressing cell migration" (P.S. Yeh, W. Wang, Y.A. Chang, C.J. Lin, J.J. Wang, R.M. </pubmed_abstract><journal>Data in brief</journal><pubmed_title>Data analyses of honokiol-induced autophagy of human glioma cells &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i>.</pubmed_title><pmcid>PMC5067977</pmcid><funding_grant_id>MOHW105-TDU-B-212-134001</funding_grant_id><funding_grant_id>SKH-8302-104-DR-22</funding_grant_id><pubmed_authors>Chen RM</pubmed_authors><pubmed_authors>Lin YW</pubmed_authors><pubmed_authors>Wu GJ</pubmed_authors><pubmed_authors>Lin CJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Data analyses of honokiol-induced autophagy of human glioma cells &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i>.</name><description>This article contains raw and processed data related to a research, "Honokiol induces autophagic cell death in malignant glioma through reactive oxygen species-mediated regulation of the p53/PI3K/Akt/mTOR signaling pathway" (C.J. Lin, T.L. Chen, Y.Y. Tseng, G.J. Wu, M.H. Hsieh, Y.W. Lin, R.M. Chen, 2016) [1]. Data were obtained by immunoblotting analyses of light chain 3 (LC3)-II, beclin-1, Akt, and mTOR in human glioma U87 MG cells and mouse glioma tissues treated with honokiol, an active constituent extracted from the bark of &lt;i>Magnolia officinalis, "&lt;/i>Honokiol induces autophagy of neuroblastoma cells through activating the PI3K/Akt/mTOR and endoplasmic reticular stress/ERK1/2 signaling pathways and suppressing cell migration" (P.S. Yeh, W. Wang, Y.A. Chang, C.J. Lin, J.J. Wang, R.M. </description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Dec</publication><modification>2025-04-05T15:56:23.803Z</modification><creation>2019-03-27T02:26:57Z</creation></dates><accession>S-EPMC5067977</accession><cross_references><pubmed>27774504</pubmed><doi>10.1016/j.dib.2016.09.045</doi></cross_references></HashMap>