Gene therapy based on interleukin-12 loaded chitosan nanoparticles in a mouse model of fibrosarcoma

Gene therapy based on interleukin-12 loaded chitosan nanoparticles in a mouse model of fibrosarcoma


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نویسندگان: سمیه حلاج نژادی , فرزانه لطفی پور بناب , بهزاد برادران , سعیده راضی صوفیانی

کلمات کلیدی: Chitosan Gene therapy IL-12 In vivo Nanoparticle Tumor

نشریه: 16525 , ندارد , 19 , 2016

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نویسنده ثبت کننده مقاله سعیده راضی صوفیانی
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز تحقیقات ایمونولوژی
کد مقاله 69710
عنوان فارسی مقاله Gene therapy based on interleukin-12 loaded chitosan nanoparticles in a mouse model of fibrosarcoma
عنوان لاتین مقاله Gene therapy based on interleukin-12 loaded chitosan nanoparticles in a mouse model of fibrosarcoma
ناشر 4
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت

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Objective(s): Interleukin-12 (IL-12) as a cytokine has been proved to have a critical role in stimulating the immune system and has been used as immunotherapeutic agents in cancer gene therapy. Chitosan as a polymer, with high ability of binding to nucleic acids is a good candidate for gene delivery since it is biodegradable, biocompatible and non-allergenic polysaccharide. The objective of the present study was to investigate the effects of cells transfected with IL-12 loaded chitosan nanoparticles on the regression of fibrosarcoma tumor cells (WEHI-164) in vivo. Materials and Methods: WEHI-164 tumor cells were transfected with IL-12 loaded chitosan nanoparticles and then were injected subcutaneously to inoculate tumor in BALB/c mice. Tumor volumes were determined and subsequently extracted after mice sacrifice. The immunohistochemistry staining was performed for analysis of Ki-67 expression (a tumor proliferation marker) in tumor masses. The expression of IL-12 and IFN-γ were studied using real-time polymerase chain reaction and immunoblotting. Results: The group treated with IL-12 loaded chitosan nanoparticles indicated decreasing of tumor mass volume (P<0.001). The results of western blotting and real-time PCR showed that the IL-12 expression was increased in the group. Immunohistochemistry staining indicated that the Ki67expression was reduced in the group treated with IL-12 loaded chitosan nanoparticles. Conclusion: IL-12 gene therapy using chitosan nan

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نویسنده نفر چندم مقاله
سمیه حلاج نژادیدوم
فرزانه لطفی پور بنابسوم
بهزاد برادرانچهارم
سعیده راضی صوفیانیاول

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IJBMS-19-1238.pdf1398/08/181125072دانلود