Silencing of HIF-1α/CD73 axis by siRNA-loaded TAT-Chitosan-SPION Nanoparticles robustly blocks cancer cell progression
Silencing of HIF-1α/CD73 axis by siRNA-loaded TAT-Chitosan-SPION Nanoparticles robustly blocks cancer cell progression
نویسندگان: فرناز حاجی زاده , صدف مقدس زاده اردبیلی , مهدی باغی مورنانی , علی مسجدی , وحید کارپیشه , سپیده ایزدی , بهزاد برادران , مهدی یوسفی , فرهاد جدیدی نیارق
کلمات کلیدی: Hypoxia inducible factor
CD73
Nanoparticle
Cancer
SPION
Chitosan
نشریه: 55157 , 1 , 882 , 2020
| نویسنده ثبت کننده مقاله |
فرهاد جدیدی نیارق |
| مرحله جاری مقاله |
تایید نهایی |
| دانشکده/مرکز مربوطه |
مرکز تحقیقات ایمونولوژی |
| کد مقاله |
71557 |
| عنوان فارسی مقاله |
Silencing of HIF-1α/CD73 axis by siRNA-loaded TAT-Chitosan-SPION Nanoparticles robustly blocks cancer cell progression |
| عنوان لاتین مقاله |
Silencing of HIF-1α/CD73 axis by siRNA-loaded TAT-Chitosan-SPION Nanoparticles robustly blocks cancer cell progression |
| ناشر |
15 |
| آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ |
بلی |
| عنوان نشریه (خارج از لیست فوق) |
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| 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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| Induction of Hypoxia Inducible Factor (HIF) as a direct consequence of oxygen deficiency in tumor tissues is a potent stimulus of CD73 (ecto-5′-nucleotidase) expression. Hypoxic environment and CD73 overexpression are associated with altered metabolism, elevated cancer cell proliferation, and tumor vascularization. Herein, a delivery system was developed for silencing CD73 and HIF-1α gene using siRNA-loaded Superparamagnetic iron oxide (SPION) nanocarriers for cancer treatment. SPIONs were encapsulated with thiolated chitosan (TC) and trimethyl chitosan (TMC) for improving their stabilization and functionalization. The nanoparticles (NPs) were about 133 nm in size, spherical, and non-toxic, and the addition of TAT peptide (derived from HIV-1 TAT protein) to TMC-TC-SPIONs significantly increased their cellular uptake by cancer cells. The produced NPs could efficiently accumulate in the tumor site, indicating their stability and targeting ability in reaching the tumor region. TAT-conjugated TMC-TC-SPIONs containing siRNAs could significantly reduce the HIF-1α and CD73 expression levels in cancer cells. Following transfection, cancer cells showed a significant reduction in migration and proliferation. Moreover, siRNA-loaded NPs could effectively reduce tumor growth and angiogenesis, as investigated by the chick chorioallantoic membrane (CAM) assay. This study suggested that TAT-TMC-TC-SPIONs can be potential nanocarrier for gene transfection in cancer therapy. Moreover, the co-silencing of CD73 and HIF-1α can be assumed as a novel anti-cancer treatment strategy with high tumor suppression potential. |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| Silencing of HIF.pdf | 1399/04/07 | 5041912 | دانلود |