Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/70804
標題: Danthron Induces DNA Damage and Inhibits DNA Repair Gene Expressions in GBM 8401 Human Brain Glioblastoma Multiforms Cells
作者: Lu, H.F.
Lai, T.Y.
Hsia, T.C.
Tang, Y.J.
Yang, J.S.
Chiang, J.H.
Lu, C.C.
Liu, C.M.
Wang, H.L.
Chung, J.G.
關鍵字: Danthron;DNA damage;Comet assay;DNA repair;Human brain glioblastoma;multiforms GBM 8401 cells;mitochondria-dependent pathways;cancer scc-4 cells;induced apoptosis;alzheimers-disease;breaks;curcumin;n18
Project: Neurochemical Research
期刊/報告no:: Neurochemical Research, Volume 35, Issue 7, Page(s) 1105-1110.
摘要: 
Our primary studies had shown that danthron induced cytotoxic effects, including apoptosis and inhibition of migration and invasion. However, danthron-affected DNA damage and repair gene expressions are not clear. In this study, we investigated to examine whether or not danthron induced DNA damage and inhibited DNA repair gene expression in human brain glioblastoma multiforms (GBM 8401) cells. The results from Comet assay indicated that incubation of GBM 8401 cells with 0, 50, 100 and 150 mu M of danthron led to a longer DNA migration smear based on the single cell electrophoresis (Comet tail). The results from real-time PCR assay demonstrated that 100 mu M of danthron for 24 h treatment in GBM 8401 cells led to decrease all examined ataxia telangiectasia mutated (ATM), ataxia-telangiectasia and Rad3-related (ATR), breast cancer 1, early onset (BRCA-1), 14-3-3 proteins sigma (14-3-3 sigma), DNA-dependent serine/threonine protein kinase (DNA-PK) and O (6) -methylguanine-DNA methyltransferase (MGMT) mRNA expressions. Taken together, the present study showed that danthron caused DNA damage and inhibited DNA repair genes, which may be the factors for danthron-inhibited cell growth in vitro.
URI: http://hdl.handle.net/11455/70804
ISSN: 0364-3190
DOI: 10.1007/s11064-010-0161-z
Appears in Collections:期刊論文

Show full item record
 

Google ScholarTM

Check

Altmetric

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.