Skip navigation

DSpace JSPUI

DSpace preserves and enables easy and open access to all types of digital content including text, images, moving images, mpegs and data sets

Learn More
DSpace logo
English
中文
  • Browse
    • Communities
      & Collections
    • Publication Year
    • Author
    • Title
    • Subject
    • Advisor
  • Search TDR
  • Rights Q&A
    • My Page
    • Receive email
      updates
    • Edit Profile
  1. NTU Theses and Dissertations Repository
  2. 醫學院
  3. 牙醫專業學院
  4. 口腔生物科學研究所
Please use this identifier to cite or link to this item: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/24945
Title: 以蛋白質體學為基礎來尋找新的口腔癌腫瘤標記
Global Proteomic-based Identification and Validation of Novel Tumor Markers for Human Oral Cancers
Authors: Chia-Chen Tai
戴佳貞
Advisor: 郭彥彬
Co-Advisor: 蕭宏昇
Keyword: 口腔癌,存活率,蛋白質體學,標的分子,乙四型胸線蛋白,
oral cancer,survival rate,proteomics,biomarker,Thymosin β4,
Publication Year : 2007
Degree: 碩士
Abstract: Oral cancer is the sixth most frequent cancer in the world. Buccal mucosa originated squamous cell carcinoma (SCC) is one of the most aggressive oral cancers. It mainly occurs in Taiwan, Central and Southeast Asia, and is closely related to the practice of tobacco smoking and betel squid chewing.
The high recurrence and low survival rates of buccal SCC remained an important focus for us to understand the pathogenesis of the disease in order to design better therapeutic strategies.
Here we applied novel proteomic technology to analyze oral cancer cell lines and paired N/T buccal SCC tissues to identify tumor-associated proteins as new oral cancer biomarkers or molecular targets. We further evaluated a novel cancer therapeutical compound deguelin global protein response in oral cancer cell line SAS. Our result showed a number of proteins were found to be significantly over-expressed or down-regulated in oral cancer cell lines and clinical samples. These increased proteins included glycolytic enzymes, heat-shock proteins, tumor antigens, cytoskeleton proteins, enzymes involved in detoxification and anti-oxidation systems, and proteins involved in mitochondrial and intracellular signaling pathways. These extensive protein variations indicate that multiple cellular pathways were involved in the process of tumorigenesis, and suggest that multiple protein molecules should be simultaneously targeted as an effective strategy to counter the disease.
In our results, at least, we have identified Thymosin β4, ubiquitin, BUB3, in addition to several novel proteins are candidates for targeted proteins in oral cancers. Validation of Thymosin β4 protein expression in N/T paired oral cancer tissue array by immunohistochemistry analysis revealed that Thymosin β4 overexpression was found mainly in late clinical stage oral cancer samples. The thymosin β4/ILK/Akt pathway analysis also showed similar trend for the activation of this pathway in oral cancers.
Altogether, the present findings also demonstrated that rich protein information can be produced by means of proteomic analysis for a better understanding of the oncogenesis and pathogenesis in a global way, which in turn is a basis for the rational designs of diagnostic and therapeutic methods in oral cancers.
URI: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/24945
Fulltext Rights: 未授權
Appears in Collections:口腔生物科學研究所

Files in This Item:
File SizeFormat 
ntu-96-1.pdf
  Restricted Access
9.5 MBAdobe PDF
Show full item record


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

社群連結
聯絡資訊
10617臺北市大安區羅斯福路四段1號
No.1 Sec.4, Roosevelt Rd., Taipei, Taiwan, R.O.C. 106
Tel: (02)33662353
Email: ntuetds@ntu.edu.tw
意見箱
相關連結
館藏目錄
國內圖書館整合查詢 MetaCat
臺大學術典藏 NTU Scholars
臺大圖書館數位典藏館
本站聲明
© NTU Library All Rights Reserved