Identification of Factors Involved in the Anti-Tumor Activity of Carnosine on Glioblastomas Using a Proteomics Approach

被引:25
作者
Asperger, Ansgar [1 ]
Renner, Christof [1 ]
Menzel, Mandy [1 ]
Gebhardt, Rolf [2 ]
Meixensberger, Juergen [1 ]
Gaunitz, Frank [1 ]
机构
[1] Univ Klinikum Leipzig AoR, Klin & Poliklin Neurochirurg, D-04103 Leipzig, Germany
[2] Univ Leipzig, Fak Med, Inst Biochem, D-04103 Leipzig, Germany
关键词
Brain tumors; Treatment; Therapy; Tumor cell biology; ADJUVANT TEMOZOLOMIDE; PROTEIN; BINDING; CHAPERONE; MUSCLE; FAMILY; OLA1; RADIOTHERAPY; CONCOMITANT; HIF-1-ALPHA;
D O I
10.3109/07357907.2010.550666
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human glioblastoma multiforme is the most malignant brain tumor in adults and is difficult to treat. Recently, it was demonstrated that the dipeptide carnosine inhibits tumor growth, but the main molecular targets are not known. Therefore, a proteomics study with glioblastoma cells treated with carnosine was performed. Two-dimensional gel electrophoresis and matrix-assisted laser desorption/ionization time of flight detected 31 proteins expressed differentially under the influence of carnosine. Finally, peptide mass fingerprinting identified the ""BCL2-associated athanogene 2"" and the ""von Hippel-Lindau binding protein 1"" among other proteins, linking the action of carnosine to protein folding and HIF-1 alpha alpha signalling.</.
引用
收藏
页码:272 / 281
页数:10
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