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EMX2 Is a Predictive Marker for Adjuvant Chemotherapy in Lung Squamous Cell Carcinomas

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单位: [1]Tianjin Med Univ, Key Lab Canc Prevent & Therapy, Dept Lung Canc,Canc Inst & Hosp, Lung Canc Ctr,Natl Clin Res Ctr Canc, Tianjin 300060, Peoples R China [2]Univ Calif San Francisco, Thorac Oncol Program, Dept Surg, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94115 USA [3]Capital Med Univ, Beijing Friendship Hosp, Dept Oncol, Beijing 100050, Peoples R China [4]Capital Med Univ, Xuanwu Hosp, Dept Thorac Surg, Beijing 100053, Peoples R China [5]Tsinghua Univ, Sch Life Sci, Beijing 10084, Peoples R China [6]Peking Univ, Canc Hosp & Inst, Thorac Surg 2, Key Lab Carcinogenesis & Translat Res,Minist Educ, Beijing 100142, Peoples R China [7]Tianjin Med Univ, Canc Inst & Hosp, Lung Canc Ctr, Dept Pathol, Tianjin 300060, Peoples R China
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Background Squamous cell carcinomas (SCC) account for approximately 30% of non-small cell lung cancer (NSCLC). Current staging methods do not adequately predict outcome for this disease. EMX2 is a homeo-domain containing transcription factor known to regulate a key developmental pathway. This study assessed the significance of EMX2 as a prognostic and predictive marker for resectable lung SCC. Methods Two independent cohorts of patients with lung SCC undergoing surgical resection were studied. EMX2 protein expression was examined by immunohistochemistry, Western blot, or immunofluorescence. EMX2 expression levels in tissue specimens were scored and correlated with patient outcomes. Chemo-sensitivity of lung SCC cell lines stably transfected with EMX2 shRNAs to cisplatin, carboplatin, and docetaxel was examined in vitro. Results EMX2 expression was down-regulated in lung SCC tissue samples compared to their matched adjacent normal tissues. Positive EMX2 expression was significantly associated with improved overall survival in stage I lung SCC patients, and in stage II/IIIA lung SCC patients receiving adjuvant chemotherapy. EMX2 expression was also associated with expression of EMT markers in both lung SCC cell lines and tissue samples. Knock-down of EMX2 expression in lung SCC cells promoted chemo-resistance and cell migration. Conclusions EMX2 expression is down-regulated in lung SCC and its down-regulation is associated with chemo-resistance in lung SCC cells, possibly through regulation of Epithelial-to-Mesenchymal Transition (EMT). EMX2 may serve as a novel prognostic marker for stage I lung SCC patients and a prediction marker for stage II/IIIA lung SCC patients receiving adjuvant chemotherapy.

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出版当年[2014]版:
大类 | 3 区 生物
小类 | 3 区 综合性期刊
最新[2025]版:
大类 | 3 区 综合性期刊
小类 | 3 区 综合性期刊
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出版当年[2013]版:
Q1 MULTIDISCIPLINARY SCIENCES
最新[2023]版:
Q1 MULTIDISCIPLINARY SCIENCES

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第一作者单位: [1]Tianjin Med Univ, Key Lab Canc Prevent & Therapy, Dept Lung Canc,Canc Inst & Hosp, Lung Canc Ctr,Natl Clin Res Ctr Canc, Tianjin 300060, Peoples R China [2]Univ Calif San Francisco, Thorac Oncol Program, Dept Surg, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94115 USA
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