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1.
Cancer Gene Ther ; 21(7): 297-303, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24948145

ABSTRACT

Glioblastoma multiforme (GBM) are intracranial tumors of the central nervous system and the most lethal among solid tumors. Current therapy is palliative and is limited to surgical resection followed by radiation therapy and temozolomide treatment. Aberrant WNT pathway activation mediates not only cancer cell proliferation but also promotes radiation and chemotherapeutic resistance. WNT antagonists such as the secreted frizzled-related protein (sFRP) family have an ability to sensitize glioma cells to chemotherapeutics, decrease proliferation rate and induce apoptosis. During tumor development, sFRP genes (1-5) are frequently hypermethylated, causing transcriptional silencing. We investigated a possible involvement of methylation-mediated silencing of the sFRP gene family in human GBM using four human glioblastoma cell lines (U87, U138, A172 and LN18). To induce demethylation of the DNA, we inhibited DNA methyltransferases through treatment with 5-azacytidine. Genomic DNA, RNA and total protein were isolated from GBM cells before and after treatment. We utilized bisulfite modification of genomic DNA to examine the methylation status of the respective sFRP promoter regions. Pharmacological demethylation of the GBM cell lines demonstrated a loss of methylation in sFRP promoter regions, as well as an increase in sFRP gene-specific mRNA abundance. Western blot analysis demonstrated an increased protein expression of sFRP-4 and increased levels of phosphorylated-ß-catenin. These data indicate an important role of methylation-induced gene silencing of the sFRP gene family in human GBM.


Subject(s)
Brain Neoplasms/genetics , Glioblastoma/genetics , Glycoproteins/genetics , Brain Neoplasms/pathology , Cell Growth Processes/genetics , Cell Line, Tumor , DNA Methylation , Epigenesis, Genetic , Gene Silencing , Glioblastoma/pathology , Glycoproteins/metabolism , Humans , Intracellular Signaling Peptides and Proteins , Membrane Proteins/genetics
3.
Int Surg ; 60(4): 208-9, 1975 Apr.
Article in English | MEDLINE | ID: mdl-1091577

ABSTRACT

Patients receiving Lamprene may develop acute abdominal symptoms which simulate an abdominal emergency. Withdrawal of the drug relieves these symptoms. The absorption of Lamprene can be increased and deposition in the reticuloendothelial system as crystals can be avoided if it is administered in an alcoholic medium.


Subject(s)
Abdomen, Acute/chemically induced , Phenazines/adverse effects , Adult , Aniline Compounds/adverse effects , Aniline Compounds/therapeutic use , Drug Hypersensitivity , Foreign-Body Reaction , Humans , Leprosy/drug therapy , Male , Mononuclear Phagocyte System/drug effects , Phenazines/metabolism , Phenazines/therapeutic use
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