Production of Human Papilloma Virus Type 16 E6 Oncoprotein as a Recombinant Protein in Eukaryotic Cells

Author(s):
H MirshahabiH Mirshahabi1, Hoorieh SoleimanjahiHoorieh Soleimanjahi1,*, Z PourpakZ Pourpak2,  Z Meshkat Z Meshkat1, ZM HassanZM Hassan1
1Dept. of Virology and Immunology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
2Dept. of Allergy and Clinical Immunology, Children Medical Center, Immunology, Asthma and Allergy Research Institute, Tehran, Iran
*Corresponding Author: Corresponding author: Hoorieh Soleimanjahi, Dept. of Virology and Immunology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran, Tel: +98-2182883561, E-mail: Email: [email protected]

International Journal of Cancer Management:Vol. 5, issue 1; e80851
Published online:Mar 31, 2012
Article type:Research Article
Received:Sep 03, 2011
Accepted:Nov 20, 2011
How to Cite:Mirshahabi H, Soleimanjahi H, Pourpak Z, Meshkat Z, Hassan Z. Production of Human Papilloma Virus Type 16 E6 Oncoprotein as a Recombinant Protein in Eukaryotic Cells. Int J Cancer Manag. 2012;5(1):e80851. doi:

Abstract

Background: Cervical cancer is one of the most important and widespread cancer which affects women. There are several causes of cervical cancer; among them HPV types 16 and 18 are the most prominent ones which are recurrent and persistent infections. These genotypes are currently about 70% of cervical cancer causes in developing countries. Due to the importance of these viruses in cervical cancer, we pioneered the production of Human Papilloma Virus type16 E6 oncoprotein as a recombinant protein in order to develop a vaccine. Two HPV oncoproteins, E6 and E7, are consistently expressed in HPV-associated cancer cells and are responsible for malignant transformation. These oncogenic proteins represent ideal target antigens for developing vaccine and immunotherapeutic strategies against HPV-associated neoplasm.
Methods: In the present study, the cloned E6-oncoprotein of HPV16 in pTZ57R/T-E6 vector was used to produce professional expression vector. The target gene was subcloned in a eukaryotic expression vector. The pcDNA3-E6 vector was propagated in E.coli strain DH5α and transfected into CHO cells 72 hours post-transfection.
Results: The transfected cells were harvested; mRNA detection and the interest protein production were confirmed by western blot analysis using specific anti E6 monoclonal antibody.
Conclusion: HPV16-E6 target protein recognized by specific antibody could be an appropriate form of protein, which can be used for further studies. Due to potential effect of this protein, its DNA construction can be used for DNA vaccine in future studies.

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© 2012, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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