Advancement and prospects of tumor gene therapy
Gene therapy is one of the most attractive fields in tumor therapy. In past decades, significant progress has been achieved. Various approaches, such as viral and non-viral vectors and physical methods, have been developed to make gene delivery safer and more efficient. Several therapeutic strategie...
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Published in | Ai zheng Vol. 30; no. 3; pp. 182 - 188 |
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Main Authors | , , , , |
Format | Journal Article |
Language | Chinese English |
Published |
England
State Key Laboratory of Oncology in South China, Guangzhou, Guangdong 510060, P. R. China
01.03.2011
CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, P. R. China%CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, P. R. China Research Department, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong 510060, P.R. China Sun Yat-sen University Cancer Center |
Subjects | |
Online Access | Get full text |
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Summary: | Gene therapy is one of the most attractive fields in tumor therapy. In past decades, significant progress has been achieved. Various approaches, such as viral and non-viral vectors and physical methods, have been developed to make gene delivery safer and more efficient. Several therapeutic strategies have evolved, including gene-based (tumor suppressor genes, suicide genes, antiangiogenic genes, cytokine and oxidative stress-based genes) and RNA-based (antisense oligonucleotides and RNA interference) approaches. In addition, immune response-based strategies (dendritic cell- and T cell-based therapy) are also under investigation in tumor gene therapy. This review highlights the progress and recent developments in gene delivery systems, therapeutic strategies, and possible clinical directions for gene therapy. |
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Bibliography: | Q522 44-1195/R Gene therapy, RNA interference, antisense RNA, tumor suppressor gene, suicide gene, oxidative stress, dendritic cells, angiogenesis, viral vector, non-viral vector Q782 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 1000-467X 1944-446X |
DOI: | 10.5732/cjc.010.10074 |