Repository logo
  • English
  • 中文
Log In
Have you forgotten your password?
  1. Home
  2. College of Medicine / 醫學院
  3. School of Dentistry / 牙醫專業學院
  4. Oral Biology / 口腔生物科學研究所
  5. Generation and Characterization of Monoclonal Antibodies Against Lung cancer
 
  • Details

Generation and Characterization of Monoclonal Antibodies Against Lung cancer

Date Issued
2008
Date
2008
Author(s)
Chen, Hui-Yu
URI
http://ntur.lib.ntu.edu.tw//handle/246246/178600
Abstract
Lung cancer is the leading cause of cancer deaths, accounting for one third of all deaths from cancer worldwide. In the United States, accounting for about 29% of all cancer deaths, are expected to happen in 2008. In Taiwan, lung cancer is the first most common cancer and the death rate is the highest among all cancers, accounting for approximately 19.7% of all cancer deaths in 2006. Lung cancer is classified clinically as small (SCLC) (15-20%) or non-small cell lung cancer (NSCLC) (80-85%) for the purposes of treatment. Current treatment options include surgical resection, platinum-based doublet chemotherapy, and radiation therapy alone or in combination. However, there are many side effects and drug resistance of these treatments. Despite these therapies, the disease is rarely curable and the prognosis is poor, with an overall 5-year survival rate of only 15%. Because monoclonal antibodies (mAbs) have the ability to target tumours, and hence enables them to improve the selectivity of other types of anticancer agent. Therapeutic antibodies have established themselves as one of the most important and fastest growing classes of drugs for cancer. In this study, we have generated 12 mAbs which were specifically against CL1-5 and did not cross-react to normal cells including NNM cells, HUVEC, PBMC and normal human tissues. Four mAbs LC-Ab 1-7, LC-Ab 2-37, LC-Ab 8-5 and LC-Ab 9-5 exhibited high specificities against CL1-5. Therefore, we focused on these 4 mAbs to further characterize their biological properties. In Western blot analysis, LC-Ab 1-7, LC-Ab 2-37 and LC-Ab 4-12 recognize a protein with M.W. 60 kDa, 120 kDa and 58 kDa, respectively. These target proteins were also identified in other cancer cell line, including SAS and MDA-MB 231 by flow cytometric analysis. Furthermore, LC-Ab 2-37, LC-Ab 8-5 and LC-Ab 9-5 can induce apoptosis of cancer cells using flow cytometric analysis. Results from immunohistochemical staining of human surgical specimen sections by LC-Ab 1-7, LC-Ab 2-37, LC-Ab 8-5 and LC-Ab 9-5 indicated that these mAbs might be promising to be applied in the diagnosis and treatment for NSCLC. According to these data, the target proteins of these mAbs and their possible usage as tumor markers and development of Ab-targeted chemotherapy is warranted.
Subjects
lung cancer
hybridoma
therapeutic antibody
apoptosis
SDGs

[SDGs]SDG3

File(s)
Loading...
Thumbnail Image
Name

ntu-97-R95450012-1.pdf

Size

23.32 KB

Format

Adobe PDF

Checksum

(MD5):f6295b78df83862e119e6de6609f2a3a

臺大位居世界頂尖大學之列,為永久珍藏及向國際展現本校豐碩的研究成果及學術能量,圖書館整合機構典藏(NTUR)與學術庫(AH)不同功能平台,成為臺大學術典藏NTU scholars。期能整合研究能量、促進交流合作、保存學術產出、推廣研究成果。

To permanently archive and promote researcher profiles and scholarly works, Library integrates the services of “NTU Repository” with “Academic Hub” to form NTU Scholars.

總館學科館員 (Main Library)
醫學圖書館學科館員 (Medical Library)
社會科學院辜振甫紀念圖書館學科館員 (Social Sciences Library)

開放取用是從使用者角度提升資訊取用性的社會運動,應用在學術研究上是透過將研究著作公開供使用者自由取閱,以促進學術傳播及因應期刊訂購費用逐年攀升。同時可加速研究發展、提升研究影響力,NTU Scholars即為本校的開放取用典藏(OA Archive)平台。(點選深入了解OA)

  • 請確認所上傳的全文是原創的內容,若該文件包含部分內容的版權非匯入者所有,或由第三方贊助與合作完成,請確認該版權所有者及第三方同意提供此授權。
    Please represent that the submission is your original work, and that you have the right to grant the rights to upload.
  • 若欲上傳已出版的全文電子檔,可使用Open policy finder網站查詢,以確認出版單位之版權政策。
    Please use Open policy finder to find a summary of permissions that are normally given as part of each publisher's copyright transfer agreement.
  • 網站簡介 (Quickstart Guide)
  • 使用手冊 (Instruction Manual)
  • 線上預約服務 (Booking Service)
  • 方案一:臺灣大學計算機中心帳號登入
    (With C&INC Email Account)
  • 方案二:ORCID帳號登入 (With ORCID)
  • 方案一:定期更新ORCID者,以ID匯入 (Search for identifier (ORCID))
  • 方案二:自行建檔 (Default mode Submission)
  • 方案三:學科館員協助匯入 (Email worklist to subject librarians)

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science