Adenoviral based gene therapy for cancer in human and animals: a review

Adenovirus vector is the most common used vector in clinical gene therapy. The development of adenovirus from the first generation until the helper-dependent adenovirus vector has greatly reduced toxicity and immunogenicity. The helper-dependent adenovirus can also prolong transgene expression. Tiss...

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Main Authors: Tan, Seok Shin, Allaudin, Zeenathul Nazariah, Mohd Lila, Mohd Azmi
Format: Article
Language:English
Published: Universiti Putra Malaysia Press 2011
Online Access:http://psasir.upm.edu.my/id/eprint/40590/
http://psasir.upm.edu.my/id/eprint/40590/1/%2317%20Pg%20129-140.pdf
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author Tan, Seok Shin
Allaudin, Zeenathul Nazariah
Mohd Lila, Mohd Azmi
author_facet Tan, Seok Shin
Allaudin, Zeenathul Nazariah
Mohd Lila, Mohd Azmi
author_sort Tan, Seok Shin
building UPM Institutional Repository
collection Online Access
description Adenovirus vector is the most common used vector in clinical gene therapy. The development of adenovirus from the first generation until the helper-dependent adenovirus vector has greatly reduced toxicity and immunogenicity. The helper-dependent adenovirus can also prolong transgene expression. Tissue- or disease-specific approach has been used to improve the specificity of adenoviral vector for cancer gene therapy. This review summarizes some adenoviral gene therapy and targeting approaches available for human cancer as well as animal cancer.
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spelling upm-405902016-01-05T08:58:31Z http://psasir.upm.edu.my/id/eprint/40590/ Adenoviral based gene therapy for cancer in human and animals: a review Tan, Seok Shin Allaudin, Zeenathul Nazariah Mohd Lila, Mohd Azmi Adenovirus vector is the most common used vector in clinical gene therapy. The development of adenovirus from the first generation until the helper-dependent adenovirus vector has greatly reduced toxicity and immunogenicity. The helper-dependent adenovirus can also prolong transgene expression. Tissue- or disease-specific approach has been used to improve the specificity of adenoviral vector for cancer gene therapy. This review summarizes some adenoviral gene therapy and targeting approaches available for human cancer as well as animal cancer. Universiti Putra Malaysia Press 2011-01 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/40590/1/%2317%20Pg%20129-140.pdf Tan, Seok Shin and Allaudin, Zeenathul Nazariah and Mohd Lila, Mohd Azmi (2011) Adenoviral based gene therapy for cancer in human and animals: a review. Pertanika Journal of Science & Technology, 19 (1). pp. 129-140. ISSN 0128-7680; ESSN: 2231-8526 http://www.pertanika.upm.edu.my/Pertanika%20PAPERS/JST%20Vol.%2019%20%281%29%20Jan.%202011/%2317%20Pg%20129-140.pdf
spellingShingle Tan, Seok Shin
Allaudin, Zeenathul Nazariah
Mohd Lila, Mohd Azmi
Adenoviral based gene therapy for cancer in human and animals: a review
title Adenoviral based gene therapy for cancer in human and animals: a review
title_full Adenoviral based gene therapy for cancer in human and animals: a review
title_fullStr Adenoviral based gene therapy for cancer in human and animals: a review
title_full_unstemmed Adenoviral based gene therapy for cancer in human and animals: a review
title_short Adenoviral based gene therapy for cancer in human and animals: a review
title_sort adenoviral based gene therapy for cancer in human and animals: a review
url http://psasir.upm.edu.my/id/eprint/40590/
http://psasir.upm.edu.my/id/eprint/40590/
http://psasir.upm.edu.my/id/eprint/40590/1/%2317%20Pg%20129-140.pdf