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    題名: Overexpression of rap-1A indicates a poor prognosis for oral cavity squamous cell carcinoma and promotes tumor cell invasion via aurora-A modulation
    作者: 蘇立仁;Chen, Chang-Han;Chuang, Hui-Ching;Huang, Chao-Cheng;Fang, Fu-Min;Huang, Hsuan-Ying;Tsai, Hsin-Ting;Su, Li-Jen;Shiu, Li-Yen;Leu, Steve;Chien, Chih-Yen
    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 Kinases;Carcinoma, Squamous Cell - enzymology;Carcinoma, Squamous Cell - genetics;Carcinoma, Squamous Cell - pathology;Cell Line, Tumor;Cell Movement;Female;Gene Expression Regulation, Neoplastic;Gene Knockdown Techniques;Humans;Immunohistochemistry;Male;Middle Aged;Mouth - enzymology;Mouth - pathology;Mouth Neoplasms - enzymology;Mouth Neoplasms - genetics;Mouth Neoplasms - pathology;Neoplasm Invasiveness;Pathology;Prognosis;Proportional Hazards Models;Protein Binding;Protein-Serine-Threonine Kinases - metabolism;rap1 GTP-Binding Proteins - genetics;rap1 GTP-Binding Proteins - metabolism;Regression Analysis;Risk Factors;RNA, Small Interfering - metabolism;Survival Analysis;Up-Regulation - genetics
    日期: 2013-02-01
    上傳時間: 2026-04-23 11:18:37 (UTC+8)
    出版者: Elsevier Inc.;United States: Elsevier Inc
    摘要: 摘要: The functions of Rap-1A in oral carcinogenesis are largely unexplored. In this study, we examined the expression of Rap-1A at different malignant stages of oral cavity squamous cell carcinoma (OCSCC). Semiquantitative RT-PCR, quantitative RT-PCR, and Western blotting were used to evaluate Rap-1A mRNA and protein expressions, respectively, in paired OCSCC patient specimens. To determine the possible correlation between Rap-1A expression and various clinical characteristics, 256 samples from patients with OCSCC were evaluated by immunohistochemical staining. Strong Rap-1A expression was a significant prognostic marker and predictor of aggressive OCSCC. The overall and disease-specific 5-year survival rates were significantly correlated with strong expression of Rap-1A (P < 0.001). Functionally, overexpressed Rap-1A could promote oral cancer cell migration and invasion by Transwell chambers and wound healing assay. Conversely, the suppression of Rap-1A expression using Rap-1A–mediated siRNA was sufficient to decrease cell motility. Furthermore, our data also illustrated that Aurora-A could not only induce mRNA and protein expressions of Rap-1A for enhancing cancer cell motility but also co-localize and form a complex with Rap-1A in the oral cancer cell line. Finally, immunohistochemical staining, indirect immunofluorescence, and Western blotting analysis of human aggressive OCSCC specimens revealed a significantly positive correlation between Rap-1A and Aurora-A expression. Taken together, our results suggest that the Aurora-A/Rap-1A pathway is associated with survival, tumor progression, and metastasis of OCSCC patients.
    其他題名: Am J Pathol
    出版者: United States: Elsevier Inc
    出版日期: 2013-02-01
    出處: The American Journal of Pathology, 2013-02, Vol.182 (2), p.516-528
    資源來源: Elsevier ScienceDirect Journals Complete
    版權: 2013 American Society for Investigative Pathology
    版權: American Society for Investigative Pathology
    版權: Copyright © 2013 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.
    識別號: ISSN: 0002-9440
    識別號: ISSN: 1525-2191
    識別號: EISSN: 1525-2191
    識別號: DOI: 10.1016/j.ajpath.2012.10.023
    識別號: PMID: 23219753
    顯示於類別:[生醫科學與工程學系] 期刊論文

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