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Prognostic Significance of MAGE-A11 in Esophageal Squamous Cell Carcinoma and Identification of Related Genes Based on DNA Microarray

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机构: [1]Hebei Med Univ, Hosp 4, Res Ctr, Shijiazhuang 050017, Hebei, Peoples R China [2]Hebei Med Univ, Hosp 4, Tumor Res Inst, Shijiazhuang, Hebei, Peoples R China
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关键词: Esophageal squamous cell carcinoma (ESCC) Melanoma-associated antigens (MAGE) MAGE-A11 Prognosis Microarray

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Background and Aims. This study aims to investigate the expression pattern of melanoma-associated antigen-A11 (MAGE-A11) in esophageal squamous cell carcinoma (ESCC) specimens and analyze its prognostic significance for ESCC patients. In addition, the purpose of our study was also to explore the biological function of MAGE-A11 in ESCC cells based on DNA microarray. Methods. Immunohistochemistry was used to detect the expression of MAGE-A11 in ESCC specimens, and its prognostic significance was analyzed by statistical analysis. DNA microarray and quantitative RT-PCR were used to explore the different expression of MAGE-A11 downstream genes in ESCC cells. Cell invasion assay and MTT assay were used to detect the effect of MAGE-A11 cDNA on the invasion and proliferation of ESCC cells. Results. Of the ESCC specimens, 59.3% showed positive MAGE-A11 expression. MAGE-A11 expression in ESCC specimens was positively associated with distant lymph node metastasis. Overall survival of ESCC patients with positive MAGE-A11 expression was shorter than in patients with negative MAGE-All expression. Multivariate Cox regression analysis showed MAGE-A11 expression is an independent poor prognostic factor for ESCC patients. Overexpression of MAGE-All changed a variety of gene expressions, which was associated with various cell functions such as protein ubiquitination, cell proliferation and apoptosis, tumor invasion and metastasis. Overexpression of MAGE-A11 directly increased the invasion and proliferation of ESCC cells. Conclusions. MAGE-A11 is an independent poor prognostic marker for ESCC patients. MAGE-A11 regulates various cell functions and directly increases the invasion and proliferation of ESCC cells. (C) 2016 IMSS. Published by Elsevier Inc.

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出版当年[2016]版:
大类 | 3 区 医学
小类 | 3 区 医学:研究与实验
最新[2025]版:
大类 | 4 区 医学
小类 | 4 区 医学:研究与实验
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出版当年[2016]版:
Q2 MEDICINE, RESEARCH & EXPERIMENTAL
最新[2023]版:
Q1 MEDICINE, RESEARCH & EXPERIMENTAL

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第一作者机构: [1]Hebei Med Univ, Hosp 4, Res Ctr, Shijiazhuang 050017, Hebei, Peoples R China [2]Hebei Med Univ, Hosp 4, Tumor Res Inst, Shijiazhuang, Hebei, Peoples R China
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通讯机构: [1]Hebei Med Univ, Hosp 4, Res Ctr, Shijiazhuang 050017, Hebei, Peoples R China [2]Hebei Med Univ, Hosp 4, Tumor Res Inst, Shijiazhuang, Hebei, Peoples R China [*1]Research Center, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei 050017, People’s Republic of China
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