Suppression of Tumorigenicity and Metastasis of Human Renal Carcinoma Cells by Infection with Retroviral Vectors Harboring the Murine Inducible Nitric Oxide Synthase Gene
العنوان: | Suppression of Tumorigenicity and Metastasis of Human Renal Carcinoma Cells by Infection with Retroviral Vectors Harboring the Murine Inducible Nitric Oxide Synthase Gene |
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المؤلفون: | Isaiah J. Fidler, Yunfang Wang, Lei Xu, Junya Yoneda, Shin Hun Juang, Qian Shi, Keping Xie |
المصدر: | Human Gene Therapy. 9:845-854 |
بيانات النشر: | Mary Ann Liebert Inc, 1998. |
سنة النشر: | 1998 |
مصطلحات موضوعية: | Genetic enhancement, Genetic Vectors, Mice, Nude, Nitric Oxide Synthase Type II, Biology, Transfection, Nitric oxide, Viral vector, Metastasis, Mice, chemistry.chemical_compound, Tumor Cells, Cultured, Genetics, medicine, Animals, Humans, Neoplasm Metastasis, Carcinoma, Renal Cell, Molecular Biology, Mice, Inbred BALB C, Kidney, Genetic Therapy, medicine.disease, Kidney Neoplasms, Nitric oxide synthase, Retroviridae, medicine.anatomical_structure, chemistry, Cancer cell, Cancer research, biology.protein, Molecular Medicine, Nitric Oxide Synthase |
الوصف: | The purpose of this study was to determine whether retrovirus-mediated transfer of the murine macrophage inducible nitric oxide synthase (iNOS) gene can inhibit tumorigenicity and metastasis of human renal cancer cells. Retroviral vectors encoding murine macrophage iNOS were constructed in the pLXSN retroviral vector with the iNOS gene under the control of a long terminal repeat promoter and a neomycin resistance gene under the control of an internal simian virus 40 promoter. Highly metastatic human renal carcinoma SN12PM6 cells were infected with control or iNOS retrovirus. Expression of iNOS was confirmed by Northern and Western blot analyses, and expression of the functional iNOS protein, i.e., production of nitric oxide (NO), was determined by measuring nitrite accumulation in culture supernatants. Noninfected or control cells produced large orthotopic tumors in the kidney of nude mice and a larger number of experimental lung metastases, whereas iNOS-infected cells produced small tumors in the kidneys and few to no lung metastases. The data indicate that the infection of human renal cancer cells by retroviruses harboring the murine iNOS gene can induce the production of high levels of NO, which is associated with autocytotoxicity, suppression of tumorigenicity, and abrogation of metastasis. |
تدمد: | 1557-7422 1043-0342 |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f604fa3b1f2867f6f482a633f391e508 https://doi.org/10.1089/hum.1998.9.6-845 |
حقوق: | CLOSED |
رقم الأكسشن: | edsair.doi.dedup.....f604fa3b1f2867f6f482a633f391e508 |
قاعدة البيانات: | OpenAIRE |
تدمد: | 15577422 10430342 |
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