Volume 17, Issue 4 (2015)                   mjms 2015, 17(4): 88-99 | Back to browse issues page

XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Kazemi M, Amani J, Salmanian A H, Forghanifard M M, Aghamollaei H. Design and Expression of Recombinant HER-2 Antigen as a Marker for Detection of Breast Cancer. mjms 2015; 17 (4) :88-99
URL: http://mjms.modares.ac.ir/article-30-52-en.html
1- Department of Biology, University of Damghan, Damghan, Iran
2- Applied biotechnology centre, Baqiyatallah University of Medical Sciences.
3- Department of Plant Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran
4- Department of Biology, University of Damghan, Damghan, Iran.
5- Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran
Abstract:   (6425 Views)
Objective: The incidence of breast cancer is approximately one million which makes this cancer one of the most common among women worldwide. Breast cancer comprises 7% of the total death rate caused by cancers. Several strategies that use tumor-associated antigen (TAA) vaccination and early detection of breast cancer are clinically being developed. Breast cancer is caused by increased over expression of certain genes. HER-2 is a tyrosine kinase receptor in the epidermal growth factor family. The role of HER-2 in breast cancer has been extensively studied. HER-2 is found in 25%-30% of breast cancer patients. Herceptin, a human antibody, is used as a therapeutic target for HER-2. The purpose of this study is to produce recombinant protein HER-2 for early detection of breast cancer cells. Methods: We used specific primers to amplify the HER-2 gene. The amplified gene was cloned into pET28a as an expression vector. Cloning was confirmed by restriction analysis and sequencing. Expression was induced using IPTG and the recombinant protein was analyzed by SDS-PAGE. Results: Cloning of the HER-2 gene was confirmed by enzyme digestion and sequencing. The gene was expressed in E.coli BL21 DE3. The pET-28a vector which contained the HER-2 gene showed a high level of expression. The recombinant protein was confirmed by Western blot analysis. Conclusions: A portion of the HER-2 gene was expressed as a recombinant in E.coli. This could be a good diagnostic test for breast cancer.
Full-Text [PDF 1021 kb]   (6756 Downloads)    
Article Type: Short Comunication | Subject: Molecular Biotechnology
Received: 2014/05/18 | Accepted: 2014/09/17

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.