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    請使用永久網址來引用或連結此文件: https://ir.lib.ncu.edu.tw/handle/987654321/102697


    題名: Aurora-A signaling is activated in advanced stage of squamous cell carcinoma of head and neck cancer and requires osteopontin to stimulate invasive behavior
    作者: 蘇立仁;Chien, Chih-Yen;Tsai, Hsin-Ting;Su, Li-Jen;Chuang, Hui-Ching;Shiu, Li-Yen;Huang, Chao-Cheng;Fang, Fu-Min;Yu, Chun-Chieh;Su, Huei-Ting;Chen, Chang-Han
    貢獻者: 生醫理工學院生醫科學與工程學系
    關鍵詞: Adult;Aged;Aged, 80 and over;Aurora Kinase A - metabolism;Blotting, Western;Carcinoma, Squamous Cell - metabolism;Carcinoma, Squamous Cell - pathology;Female;Head and Neck Neoplasms - metabolism;Head and Neck Neoplasms - pathology;Humans;Immunohistochemistry;Kaplan-Meier Estimate;Male;MAP Kinase Signaling System - physiology;Middle Aged;Neoplasm Invasiveness - physiopathology;Oligonucleotide Array Sequence Analysis;Osteopontin - metabolism;Proportional Hazards Models;Real-Time Polymerase Chain Reaction;Research Paper;Reverse Transcriptase Polymerase Chain Reaction;Signal Transduction - physiology;Squamous Cell Carcinoma of Head and Neck;Transfection
    日期: 2014-01-01
    上傳時間: 2026-04-23 11:15:12 (UTC+8)
    出版者: Impact Journals LLC;United States: Impact Journals LLC
    摘要: 摘要: The clinical significances, cellular effects, and molecular mechanisms by which Aurora-A mediate its invasive effects in HNSCC are still unclear. Here, we found that Aurora-A expression is significantly higher in tumor tissues on 14-microarray of HNSCC in Oncomine-databases. The activity of Aurora-A was not only found in HNSCC specimens, but also significantly correlated with advanced-T-classification, positive-N-classification, TNM-stage and the poor 5-year survival rate. HNSCC-microarray profile showed that osteopontin and Aurora-A exhibited positive correlation. Stimulation of HNC cells with osteopontin results in an increase in Aurora-A expression where localized at the centrosome. Functionally, Aurora-A had the abilities to stimulate cell motility in HNC cells through increase ERK1/2 activity under osteopontin stimulation. Conversely, depletion of Aurora-A expression by siRNAs suppressed ERK1/2 activity as well as inhibition of cell invasiveness. Treatment with anti-CD44 antibodies in HNC cells not only caused a decrease of mRNA/protein of Aurora-A and ERK1/2 activity upon osteopontin stimulation, but also affected the abilities of Aurora-A-elicited cell motility. Finally, immunohistochemical/Western-blotting analysis of human aggressive HNSCC specimens showed a significant positively correlation between osteopontin-Aurora-A and ERK1/2. These findings suggest that Aurora-A is not only an important prognostic factor but also a new therapeutic target in the osteopontin/CD44/ERK pathway for HNSCC treatment.
    其他題名: Oncotarget
    出版者: United States: Impact Journals LLC
    出版日期: 2014-04-30
    出處: Oncotarget, 2014-04, Vol.5 (8), p.2243-2262
    版權: Copyright: © 2014 Chien et al. 2014
    識別號: ISSN: 1949-2553
    識別號: EISSN: 1949-2553
    識別號: DOI: 10.18632/oncotarget.1896
    識別號: PMID: 24810160
    顯示於類別:[生醫科學與工程學系] 期刊論文

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