2.Herpes Viral Gene Therapy for the Treatment of Head and Neck Squamous Cell Carcinoma.
Korean Journal of Otolaryngology - Head and Neck Surgery 2006;49(5):474-481
No Abstract available.
Carcinoma, Squamous Cell*
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Genes, Viral*
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Head*
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Neck*
3.Therapeutic Angiogenesis: The Pros and Cons and the Future.
Korean Circulation Journal 2008;38(2):73-79
Despite the improvements in medical, surgical and endovascular therapies, vascular disease is still a significant, critical clinical problem. The advances in understanding the mechanisms of neovascularization and the accumulated experiences of successful therapeutic application in animal models have raised expectations for therapeutic angiogenesis as a promising treatment option. However, the large, double-blinded, controlled clinical trials using therapeutic agent in the form of protein, naked DNA or viral gene therapy have failed to show clinical benefit. Nevertheless, by this time, cell based therapeutic angiogenesis has raised a promising option for the treatment of ischemic diseases. This article summarizes the essential preclinical research and major clinical trials on therapeutic angiogenesis, and it deals with several issues related to the failure of the clinical trials. Future directions in the realm of therapeutic angiogenesis are also described with focusing on cell based therapy.
DNA
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Genes, Viral
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Models, Animal
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Tissue Therapy
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Vascular Diseases
4.Effects of mutation of hepatitis B virus poly(A) signal "TATAAA" to "AATAAA" on expression of hepatitis B viral genes.
Sang Hae KIM ; Seong Kee KIM ; Yong Tae KWON ; Hyune Mo RHO
Journal of the Korean Society of Virology 1992;22(1):37-44
No abstract available.
Genes, Viral*
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Hepatitis B virus*
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Hepatitis B*
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Hepatitis*
6.Analysis of genetic characteristics of wild-type measles viruses in Jilin Province 2005.
Jiang BIAN ; Fan LI ; Shi-hong YI
Chinese Journal of Preventive Medicine 2006;40(5):348-350
OBJECTIVETo investigate the know gene types of main wild type measles virus strains and take measures to control measles in Jilin Province.
METHODSGenetic characterization of 9 measles viruses isolated from 72 throat swabs or urine specimens of measles patients using CDW(150) cells line was studied in Jilin Province in 2005.
RESULTSSequence analysis of 450 nucleotides of COOH-terminal of nucleoprotein (N) genes of 9 isolates indicated that all were members of H(1) genotype, in which there are 7 strains of H1a and 2 strains of H1b, the H1a subgroup differed from H1b by 2.0% approximately 3.5% at the nucleotide level in the COOH-terminal of the N gene.
CONCLUSIONSThe H(1) genotype of wild-type measles viruses should be the main epidemic strain and main pathogen that caused measles outbreaks and sporadic cases in Jilin Province.
China ; Genes, Reporter ; Genes, Viral ; Genotype ; Humans ; Measles ; epidemiology ; virology ; Measles virus ; genetics ; Molecular Sequence Data ; Viral Structural Proteins ; genetics
7.The construction of a novel recombinant virus Δ67R-RGV and preliminary analyses the function of the 67R gene.
Xing HUANG ; Chao PEI ; Li-Bo HE ; Qi-Ya ZHANG
Chinese Journal of Virology 2014;30(5):495-501
The Rana grylio virus (RGV) is a member of the genus Ranavirus. It belongs to the family Iridoviridae, and contains the gene 67R encoding dUTPase. In order to investigate the function of 67R in the replication and infection of RGV, we constructed Δ67R-RGV, a recombinant virus with deletion of 67R. First, we constructed the plasmid pGL3-67RL-p50-EGFP-67RR which carried an enhanced green fluorescence gene (EGFP) as a selectable marker. After homologous recombination between pGL3-67RL-p50-EG- FP-67RR and the RGV genome, Epithelioma papulosum cyprini (EPC) cells were infected with the resulting mixture. Through ten successive rounds of plaque isolation via EGFP selection, all plaques emitted green fluorescence, and finally Δ67R-RGV was generated. Total DNA of Δ67R-RGV infected cells was extracted for PCR analyses. Simulateously, mock infected and wild-type RGV (wt-RGV) infected cells were used as a comparison. Results showed that 67R could be detected in wt-RGV infected cells, but that only the EGFP gene was detected in Δ67R-RGV infected cells. Furthermore, one-step growth curves of wt-RGV and Δ67R-RGV were similar. Therefore, 67R and its encoding product dUTPase might not be essential for the growth of RGV. These results suggest that, homologous recombination and recombinant rana- virus could be used to study the gene function of viruses in aquatic animals.
Genes, Viral
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physiology
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Genome, Viral
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Polymerase Chain Reaction
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Pyrophosphatases
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genetics
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Ranavirus
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genetics
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Recombination, Genetic
10.Molecular analysis on the S gene of three Crimean-Congo hemorrhagic fever virus strains in China.
Su-rong SUN ; Wei-wei MENG ; Yu-jiang ZHANG ; Xin-hui WANG ; Azati ; Xiang DAI ; Han-ping ZHU ; Chong-hui FENG ; Ji MA ; Fu-chun ZHANG ; Yan-xiang XIE ; Chang-shou HANG
Chinese Journal of Epidemiology 2006;27(10):880-883
OBJECTIVETo compare the molecular characteristics of 3 Crimean-Congo hemorrhagic fever viruses(CCHFV) isolated in Xinjiang province.
METHODSYL05035, YT05099 and LT05146 were isolated in 2005 from Hyalomma ticks and viral RNA was extracted from suckling mouse brains infected with these three strains respectively. The polymerase chain reaction(PCR) products of S segments from the 3 strains of CCHFV were directly sequenced.
RESULTSThe full-length'S RNA from the 3 strains of CCHFV all comprised 1673 nucleotides with ORF of them including 1449 nucleotides and encoding a protein which comprised 482 amino acids in a viral complementary sense. The sequences indicated that the three strains of CCHFV isolated from ticks in Xinjiang province were highly homologenic. Data from the phylogenetic analysis showed that the obtained sequences were identical. The homology between 3 strains of CCHFV was 99.5%. Their homologies compared with that of the other strains isolated from other region of Xinjiang were also high at nucleotide levels (92.7%-99.8%). The three strains which were clustered together with 7001 strain and 79121 strain (isolated from patient and rat in Xinjiang respectively) was only different by 2%-3%. The genetic difference from the prototype CCHFV Nigerian strain IBAR10200 was 13%. In comparison, the Nigerian CCHFV tick isolate was more divergent when compared with the reference China strains 66019 and with the three variants mentioned above.
CONCLUSIONThe CCHFV isolated from China comprised a group of genetically high conserved strains.
Animals ; Brain ; virology ; China ; Genes, Viral ; Hemorrhagic Fever Virus, Crimean-Congo ; genetics ; isolation & purification ; Mice ; RNA, Viral ; analysis