Differences in Protein Expression between the U251 and U87 Cell Lines

被引:54
作者
Li, Hezhen [1 ]
Lei, Bingxi [1 ]
Xiang, Wei [1 ]
Wang, Hai [1 ]
Feng, Wenfeng [1 ]
Liu, Yawei [2 ]
Qi, Songtao [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Nanfang Glioma Ctr, Dept Neurosurg, Guangzhou, Guangdong, Peoples R China
[2] Southern Med Univ, Nanfang Hosp, Nanfang Neurosurg Res Inst, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Glioblastoma; U87 cell line; U251 cell line; Proteome; Gene ontology; PURINE NUCLEOSIDE PHOSPHORYLASE; THERAPEUTIC TARGET; METABOLISM; GLIOBLASTOMA; INHIBITORS;
D O I
10.5137/1019-5149.JTN.17746-16.1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
AIM: The U251 and U87 cell lines are commonly used as experimental models of glioblastoma. However, these cells exhibit significant differences in their proliferation, invasion, and migration. The aim of the present study was to compare the protein expression profiles of the U251 and U87 cell lines in order to provide a molecular basis for the observed phenotypic differences. MATERIAL AND METHODS: Isobaric tags for relative and absolute quantitation (iTRAQ) and gene ontology (GO) analyses were performed to detect differentially expressed proteins and to predict protein functions, respectively. RESULTS: Two hundred and forty-four proteins were highly expressed, while 263 proteins exhibited lower levels of expression, in the U251 cells compared to the U87 cells. In particular, higher expression levels of the proteins, C10orf58, FLNC, PDLIM1, TPM4, and lower expression levels of MYH10, PSIP1, SYNM, SLC9A3R2, BCAM, were verified by qPCR in the U251 cell line versus the U87 cell line. When a GO analysis was applied to the iTRAQ results, the proteins that were highly expressed in the U251 cells were found to differ in their molecular functions, biological processes, cellular distribution, and cellular pathways associated with them compared with the highly expressed proteins detected in the U87 cells. CONCLUSION: Differentially expressed proteins between the U251 and U87 cell lines are associated with regulation of nicotinamide nucleotide metabolism, RNA splicing, glycolysis, and purine metabolism pathways. Further studies on these pathways may identify whether these various pathways account for the observed phenotype differences between the U87 and U251 GBM cell lines.
引用
收藏
页码:894 / 903
页数:10
相关论文
共 21 条
  • [1] ALLISON AC, 1993, SPRINGER SEMIN IMMUN, V14, P353
  • [2] Silencing VDAC1 Expression by siRNA Inhibits Cancer Cell Proliferation and Tumor Growth In Vivo
    Arif, Tasleem
    Vasilkovsky, Lilia
    Refaely, Yael
    Konson, Alexander
    Shoshan-Barmatz, Varda
    [J]. MOLECULAR THERAPY-NUCLEIC ACIDS, 2014, 3 : e159
  • [3] Gene Ontology: tool for the unification of biology
    Ashburner, M
    Ball, CA
    Blake, JA
    Botstein, D
    Butler, H
    Cherry, JM
    Davis, AP
    Dolinski, K
    Dwight, SS
    Eppig, JT
    Harris, MA
    Hill, DP
    Issel-Tarver, L
    Kasarskis, A
    Lewis, S
    Matese, JC
    Richardson, JE
    Ringwald, M
    Rubin, GM
    Sherlock, G
    [J]. NATURE GENETICS, 2000, 25 (01) : 25 - 29
  • [4] G-6-PD AND PGM PHENOTYPES OF 16 CONTINUOUS HUMAN TUMOR CELL LINES - EVIDENCE AGAINST CROSS-CONTAMINATION AND CONTAMINATION BY HELA CELLS
    BECKMAN, G
    BECKMAN, L
    PONTEN, J
    WESTERMARK, B
    [J]. HUMAN HEREDITY, 1971, 21 (03) : 238 - +
  • [5] Di Stefano G, 2013, CURR TOP MED CHEM, V13, P2918
  • [6] Methotrexate inhibits the first committed step of purine biosynthesis in mitogen-stimulated human T-lymphocytes:: a metabolic basis for efficacy in rheumatoid arthritis?
    Fairbanks, LD
    Rückemann, K
    Qiu, Y
    Hawrylowicz, CM
    Richards, DF
    Swaminathan, R
    Kirschbaum, B
    Simmonds, HA
    [J]. BIOCHEMICAL JOURNAL, 1999, 342 : 143 - 152
  • [7] A proof-of-principle pharmacokinetic, pharmacodynamic, and clinical study with purine nucleoside phosphorylase inhibitor immucillin-H (BCX-1777, forodesine)
    Gandhi, V
    Kilpatrick, JM
    Plunkett, W
    Ayres, M
    Harman, L
    Du, M
    Bantia, S
    Davisson, J
    Wierda, WG
    Faderl, S
    Kantarjian, H
    Thomas, D
    [J]. BLOOD, 2005, 106 (13) : 4253 - 4260
  • [8] Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method
    Livak, KJ
    Schmittgen, TD
    [J]. METHODS, 2001, 25 (04) : 402 - 408
  • [9] MIR517C inhibits autophagy and the epithelial-to-mesenchymal (-like) transition phenotype in human glioblastoma through KPNA2-dependent disruption of TP53 nuclear translocation
    Lu, Yuntao
    Xiao, Limin
    Liu, Yawei
    Wang, Hai
    Li, Hong
    Zhou, Qiang
    Pan, Jun
    Lei, Bingxi
    Huang, Annie
    Qi, Songtao
    [J]. AUTOPHAGY, 2015, 11 (12) : 2213 - 2232
  • [10] PANTHER in 2013: modeling the evolution of gene function, and other gene attributes, in the context of phylogenetic trees
    Mi, Huaiyu
    Muruganujan, Anushya
    Thomas, Paul D.
    [J]. NUCLEIC ACIDS RESEARCH, 2013, 41 (D1) : D377 - D386