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犬细小病毒ns1基因和鸡贫血病毒vp3基因诱导犬传染性性病肿瘤部分溶瘤。

Canine Parvovirus ns1 gene and Chicken Anemia vp3 gene induce partial oncolysis of Canine Transmissible Venereal Tumor.

作者信息

Bhat Aubid Hussain, Ganguly Bhaskar, Tiwari Ashok Kumar, Das Arup Kumar

机构信息

Department of Surgery and Radiology, College of Veterinary & Animal Sciences, G. B. Pant University of Agriculture & Technology, Pantnagar, 263145, India.

Animal Biotechnology Center, Department of Veterinary Physiology and Biochemistry, College of Veterinary & Animal Sciences, G. B. Pant University of Agriculture & Technology, Pantnagar, 263145, India.

出版信息

Sci Rep. 2017 Nov 13;7(1):15419. doi: 10.1038/s41598-017-15734-6.

Abstract

The oncolytic effect of Canine Parvovirus ns1 gene and Chicken Anemia vp3 gene in naturally occurring cases of Canine Transmissible Venereal Tumor (CTVT) is being reported. Dogs suffering from CTVT (N = 18) were systematically randomized into three groups viz. A, B, and C (n = 6). Animals of the groups A, B, and C received 100 µg of the ns1 gene, vp3 gene, and ns1  +  vp3 gene combination, respectively, for three weeks intratumorally at weekly intervals; results were normalized against base values before commencement of therapy and after complete remission that were taken as negative and positive controls, respectively. Initiation of oncolytic gene therapy arrested the further progression of the tumor but most of the animals in the study underwent incomplete remission, indicating incomplete activity of ns1 and vp3 genes. The oncolytic effect of the treatments was in the order ns1 > vp3 > ns1 + vp3. Oncolysis was accompanied by decreased mitotic index and AgNOR count, and increased TUNEL positive cells and CD4 lymphocyte counts. Our findings show that Canine Parvovirus ns1 may eventually find an important role as an oncolytic agent.

摘要

本文报道了犬细小病毒ns1基因和鸡贫血病毒vp3基因对自然发生的犬传染性性病肿瘤(CTVT)的溶瘤作用。患有CTVT的犬(N = 18)被系统随机分为三组,即A组、B组和C组(每组n = 6)。A组、B组和C组的动物分别接受100μg的ns1基因、vp3基因和ns1 + vp3基因组合,每周一次,瘤内注射三周;结果以治疗开始前的基础值和完全缓解后的基础值进行标准化,分别作为阴性和阳性对照。溶瘤基因治疗的启动阻止了肿瘤的进一步进展,但研究中的大多数动物出现不完全缓解,表明ns1和vp3基因的活性不完全。治疗的溶瘤效果顺序为ns1>vp3>ns1 + vp3。溶瘤伴随着有丝分裂指数和AgNOR计数的降低,以及TUNEL阳性细胞和CD4淋巴细胞计数的增加。我们的研究结果表明,犬细小病毒ns1最终可能会作为一种溶瘤剂发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95f0/5684217/87958948d7d6/41598_2017_15734_Fig1_HTML.jpg

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