Matches in SemOpenAlex for { <https://semopenalex.org/work/W2330601121> ?p ?o ?g. }
- W2330601121 endingPage "29130" @default.
- W2330601121 startingPage "29116" @default.
- W2330601121 abstract "// Yu-Chen Cheng 1 , Dueng-Yuan Hueng 2, 3 , Hua-Yin Huang 1 , Jang-Yi Chen 4 , Ying Chen 1, 4 1 Graduate Institute of Life Science, National Defense Medical Center, Taipei, Taiwan 2 Department of Neurological Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan 3 Department of Biochemistry, National Defense Medical Center, Taipei, Taiwan 4 Department of Biology and Anatomy, National Defense Medical Center, Taipei, Taiwan Correspondence to: Ying Chen, e-mail: ychen0523@mail.ndmctsgh.edu.tw Keywords: honokiol, magnolol, autophagy, apoptosis, glioblastoma Received: November 30, 2015 Accepted: March 28, 2016 Published: April 11, 2016 ABSTRACT Glioblastoma (GBM) is a malignant brain tumor associated with a high mortality rate. The aim of this study is to investigate the synergistic effects of honokiol (Hono) and magnolol (Mag), extracted from Magnolia officinalis , on cytotoxicity and inhibition of human GBM tumor progression in cellular and animal models. In comparison with Hono or Mag alone, co-treatment with Hono and Mag (Hono-Mag) decreased cyclin A, D1 and cyclin-dependent kinase 2, 4, 6 significantly, leading to cell cycle arrest in U87MG and LN229 human glioma cells. In addition, phosphorylated phosphoinositide 3-kinase (p-PI3K), p-Akt, and Ki67 were decreased after Hono-Mag treatment, showing proliferation inhibition. Hono-Mag treatment also reduced p-p38 and p-JNK but elevated p-ERK expression. Besides, Hono-Mag treatment induced autophagy and intrinsic and extrinsic apoptosis. Both ERK and autophagy inhibitors enhanced Hono-Mag-induced apoptosis in LN229 cells, indicating a rescuer role of ERK. In human GBM orthotopic xenograft model, the Hono-Mag treatment inhibited the tumor progression and induced apoptosis more efficiently than Temozolomide, Hono, or Mag group. In conclusion, the Hono-Mag exerts a synergistic anti-tumor effect by inhibiting cell proliferation and inducing autophagy and apoptosis in human GBM cells. The Hono-Mag may be applied as an adjuvant therapy to improve the therapeutic efficacy of GBM treatment." @default.
- W2330601121 created "2016-06-24" @default.
- W2330601121 creator A5001354705 @default.
- W2330601121 creator A5012160359 @default.
- W2330601121 creator A5012778270 @default.
- W2330601121 creator A5040558103 @default.
- W2330601121 creator A5044664334 @default.
- W2330601121 date "2016-04-11" @default.
- W2330601121 modified "2023-09-23" @default.
- W2330601121 title "Magnolol and honokiol exert a synergistic anti-tumor effect through autophagy and apoptosis in human glioblastomas" @default.
- W2330601121 cites W1531380847 @default.
- W2330601121 cites W1613802206 @default.
- W2330601121 cites W1667222429 @default.
- W2330601121 cites W1961652302 @default.
- W2330601121 cites W1964068675 @default.
- W2330601121 cites W1970537994 @default.
- W2330601121 cites W1975290731 @default.
- W2330601121 cites W1980007697 @default.
- W2330601121 cites W1982626083 @default.
- W2330601121 cites W1988028506 @default.
- W2330601121 cites W1991843136 @default.
- W2330601121 cites W1999207367 @default.
- W2330601121 cites W2020812892 @default.
- W2330601121 cites W2023157569 @default.
- W2330601121 cites W2024824408 @default.
- W2330601121 cites W2029992911 @default.
- W2330601121 cites W2034213658 @default.
- W2330601121 cites W2034437737 @default.
- W2330601121 cites W2035258932 @default.
- W2330601121 cites W2042817175 @default.
- W2330601121 cites W2043520821 @default.
- W2330601121 cites W2049856484 @default.
- W2330601121 cites W2063702713 @default.
- W2330601121 cites W2065448275 @default.
- W2330601121 cites W2067777145 @default.
- W2330601121 cites W2070580147 @default.
- W2330601121 cites W2072953109 @default.
- W2330601121 cites W2079786467 @default.
- W2330601121 cites W2082748245 @default.
- W2330601121 cites W2088919658 @default.
- W2330601121 cites W2094181092 @default.
- W2330601121 cites W2096287682 @default.
- W2330601121 cites W2104174197 @default.
- W2330601121 cites W2115862526 @default.
- W2330601121 cites W2117263216 @default.
- W2330601121 cites W2129610686 @default.
- W2330601121 cites W2134338026 @default.
- W2330601121 cites W2134368529 @default.
- W2330601121 cites W2147114673 @default.
- W2330601121 cites W2148931486 @default.
- W2330601121 cites W2167426480 @default.
- W2330601121 cites W2170298919 @default.
- W2330601121 cites W2175167187 @default.
- W2330601121 cites W2265755372 @default.
- W2330601121 cites W2305987037 @default.
- W2330601121 cites W79400203 @default.
- W2330601121 cites W1904809541 @default.
- W2330601121 doi "https://doi.org/10.18632/oncotarget.8674" @default.
- W2330601121 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5045382" @default.
- W2330601121 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27074557" @default.
- W2330601121 hasPublicationYear "2016" @default.
- W2330601121 type Work @default.
- W2330601121 sameAs 2330601121 @default.
- W2330601121 citedByCount "45" @default.
- W2330601121 countsByYear W23306011212016 @default.
- W2330601121 countsByYear W23306011212017 @default.
- W2330601121 countsByYear W23306011212018 @default.
- W2330601121 countsByYear W23306011212019 @default.
- W2330601121 countsByYear W23306011212020 @default.
- W2330601121 countsByYear W23306011212021 @default.
- W2330601121 countsByYear W23306011212022 @default.
- W2330601121 countsByYear W23306011212023 @default.
- W2330601121 crossrefType "journal-article" @default.
- W2330601121 hasAuthorship W2330601121A5001354705 @default.
- W2330601121 hasAuthorship W2330601121A5012160359 @default.
- W2330601121 hasAuthorship W2330601121A5012778270 @default.
- W2330601121 hasAuthorship W2330601121A5040558103 @default.
- W2330601121 hasAuthorship W2330601121A5044664334 @default.
- W2330601121 hasBestOaLocation W23306011211 @default.
- W2330601121 hasConcept C184235292 @default.
- W2330601121 hasConcept C185592680 @default.
- W2330601121 hasConcept C190283241 @default.
- W2330601121 hasConcept C199835354 @default.
- W2330601121 hasConcept C203522944 @default.
- W2330601121 hasConcept C2781009524 @default.
- W2330601121 hasConcept C2781334404 @default.
- W2330601121 hasConcept C29537977 @default.
- W2330601121 hasConcept C502942594 @default.
- W2330601121 hasConcept C55493867 @default.
- W2330601121 hasConcept C57074206 @default.
- W2330601121 hasConcept C71924100 @default.
- W2330601121 hasConcept C75217442 @default.
- W2330601121 hasConcept C86554907 @default.
- W2330601121 hasConcept C98274493 @default.
- W2330601121 hasConceptScore W2330601121C184235292 @default.
- W2330601121 hasConceptScore W2330601121C185592680 @default.
- W2330601121 hasConceptScore W2330601121C190283241 @default.
- W2330601121 hasConceptScore W2330601121C199835354 @default.