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AJAP1 is Dysregulated at an Early Stage of Gliomagenesis and Suppresses Invasion Through Cytoskeleton Reorganization

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机构: [1]Tianjin Med Univ, Gen Hosp, Dept Neurosurg, Tianjin, Peoples R China; [2]Tianjin Neurol Inst, Tianjin 300052, Peoples R China; [3]Minist Educ, Key Lab Posttrauma Neurorepair & Regenerat Cent N, Tianjin, Peoples R China; [4]Tianjin Key Lab Injuries Variat & Regenerat Nervo, Tianjin, Peoples R China; [5]Nanjing Med Univ, Affiliated Hosp 1, Dept Neurosurg, Nanjing, Jiangsu, Peoples R China; [6]Duke Univ, Med Ctr, Preston Robert Tisch Brain Tumor Ctr, Dept Surg, Durham, NC 27710 USA; [7]Duke Univ, Med Ctr, Preston Robert Tisch Brain Tumor Ctr, Dept Neurobiol, Durham, NC 27710 USA; [8]Durham VA Med Ctr, Durham, NC USA; [9]Capital Med Univ, Tiantan Hosp, Dept Neurosurg, Beijing, Peoples R China; [10]Duke Univ, Med Ctr, Preston Robert Tisch Brain Tumor Ctr, Dept Pathol, Durham, NC 27710 USA; [11]Tianjin Neurol Inst, Lab Neurooncol, 154 Anshan Rd, Tianjin 300052, Peoples R China
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关键词: Invasion AJAP1 Glioma Proliferation Cytoskeleton

摘要:
Aims Down-regulation of AJAP1 in glioblastoma multiforme (GBM) has been reported. However, the expression profiles of AJAP1 in gliomas and the underlying mechanisms of AJAP1 function on invasion are still poorly understood. Methods The gene profiles of AJAP1 in glioma patients were studied among four independent cohorts. Confocal imaging was used to analyze the AJAP1 localization. After AJAP1 overexpression in GBM cell lines, cellular polarity, cytoskeleton distribution, and antitumor effect were investigated in vitro and in vivo. Results AJAP1 expression was significantly decreased in gliomas compared with normal brain in REMBRANDT and CGCA cohorts. Additionally, low AJAP1 expression was associated with worse survival in GBMs in REMBRANDT and TCGA U133A cohorts and was significantly associated with classical and mesenchymal subtypes of GBMs among four cohorts. Confocal imaging indicated AJAP1 localized in cell membranes in low-grade gliomas and AJAP1-overexpressing GBM cells, but difficult to assess in high-grade gliomas due to its absence. AJAP1 overexpression altered the cytoskeleton and cellular polarity in vitro and inhibited the tumor growth in vivo. Conclusions AJAP1 is dysregulated at an early stage of gliomagenesis and may suppress glioma cell invasion and proliferation, which suggests that AJAP1 may be a potential diagnostic and prognostic marker for gliomas.

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出版当年[2013]版:
大类 | 2 区 医学
小类 | 2 区 药学 3 区 神经科学
最新[2023]版:
大类 | 1 区 医学
小类 | 2 区 神经科学 2 区 药学
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出版当年[2012]版:
Q1 NEUROSCIENCES Q1 PHARMACOLOGY & PHARMACY
最新[2023]版:
Q1 PHARMACOLOGY & PHARMACY Q1 NEUROSCIENCES

影响因子: 最新[2023版] 最新五年平均 出版当年[2012版] 出版当年五年平均 出版前一年[2011版] 出版后一年[2013版]

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第一作者机构: [1]Tianjin Med Univ, Gen Hosp, Dept Neurosurg, Tianjin, Peoples R China; [2]Tianjin Neurol Inst, Tianjin 300052, Peoples R China; [3]Minist Educ, Key Lab Posttrauma Neurorepair & Regenerat Cent N, Tianjin, Peoples R China; [4]Tianjin Key Lab Injuries Variat & Regenerat Nervo, Tianjin, Peoples R China;
通讯作者:
通讯机构: [1]Tianjin Med Univ, Gen Hosp, Dept Neurosurg, Tianjin, Peoples R China; [2]Tianjin Neurol Inst, Tianjin 300052, Peoples R China; [3]Minist Educ, Key Lab Posttrauma Neurorepair & Regenerat Cent N, Tianjin, Peoples R China; [4]Tianjin Key Lab Injuries Variat & Regenerat Nervo, Tianjin, Peoples R China; [6]Duke Univ, Med Ctr, Preston Robert Tisch Brain Tumor Ctr, Dept Surg, Durham, NC 27710 USA; [7]Duke Univ, Med Ctr, Preston Robert Tisch Brain Tumor Ctr, Dept Neurobiol, Durham, NC 27710 USA; [11]Tianjin Neurol Inst, Lab Neurooncol, 154 Anshan Rd, Tianjin 300052, Peoples R China
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