The miR-365a caused down regulation of antioxidant proteins and ROS accumulation in HepG2 cells

The miR-365a caused down regulation of antioxidant proteins and ROS accumulation in HepG2 cells


چاپ صفحه
پژوهان
صفحه نخست سامانه
نویسندگان
نویسندگان
اطلاعات تفضیلی
اطلاعات تفضیلی
دانلود مقاله
دانلود مقاله
دانشگاه علوم پزشکی تبریز
دانشگاه علوم پزشکی تبریز

نویسندگان: آرمیتا قوطاسلو , آرزو عزیزسلطانی , عفت علیزاده

عنوان کنگره / همایش: هشتمین کنفرانس بین المللی زیست پزشکی 2024 , Iran (Islamic Republic) , Tehran , 2024

اطلاعات کلی مقاله
hide/show

نویسنده ثبت کننده مقاله عفت علیزاده
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه دانشکده علوم نوین پزشکی
کد مقاله 86391
عنوان فارسی مقاله The miR-365a caused down regulation of antioxidant proteins and ROS accumulation in HepG2 cells
عنوان لاتین مقاله The miR-365a caused down regulation of antioxidant proteins and ROS accumulation in HepG2 cells
نوع ارائه پوستر
عنوان کنگره / همایش هشتمین کنفرانس بین المللی زیست پزشکی 2024
نوع کنگره / همایش بین المللی
کشور محل برگزاری کنگره/ همایش Iran (Islamic Republic)
شهر محل برگزاری کنگره/ همایش Tehran
سال انتشار/ ارائه شمسی 1403
سال انتشار/ارائه میلادی 2024
تاریخ شمسی شروع و خاتمه کنگره/همایش 1403/08/19 الی 1403/08/29
آدرس لینک مقاله/ همایش در شبکه اینترنت
آدرس علمی (Affiliation) نویسنده متقاضی Department of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran

نویسندگان
hide/show

نویسنده نفر چندم مقاله
آرمیتا قوطاسلواول
آرزو عزیزسلطانیدوم
عفت علیزادهسوم

اطلاعات تفضیلی
hide/show

عنوان متن
خلاصه مقالهIntroduction Hepatocellular carcinoma (HCC), a deadly form of liver cancer, is influenced by miRNAs and imbalances in redox homeostasis. Cancer cells adapt themselves to high oxidative stress by increasing self-antioxidant levels. MicroRNA-365a-3p (miR-365a-3p) has emerged as a critical regulator of cellular processes, yet its specific role in oxidative stress within liver cells remains poorly understood. This study investigates the effects of miR-365a on antioxidant protein expression, reactive oxygen species (ROS) levels, and apoptosis in HepG2 cells. Material and methods The miR-365a mimic was delivered to HCC cells using Lipofectamine reagent. Next, the effect of the miR-365a-3p on intracellular ROS was detected using DCFDA method. The network of proteins involved in oxidative responses were extracted from String Database then two key proteins downstream to Nrf2 protein including superoxide dismutase1 (SOD1) and, Heme Oxygenase 1(HO-1) were selected. Finally, the effect of miR-365a-3p treatment on levels of HO1, and SOD1 proteins were investigated using western blot. Apoptosis was detected by flowcytometry. Results & Discussion We found that the increasing intracellular levels of miR-365a-3p led to a marked downregulation of key antioxidant proteins, including SOD1 and HO-1. Consequently, this downregulation resulted in a significant accumulation of ROS, indicating a failure of cancer cell antioxidant performance and accumulation of ROS. Such high levels of ROS massive programmed death in HepG2 cells. Conclusion Our results suggest that miR-365a-3p may play a pivotal role in modulating oxidative stress responses in HepG2 cells which results in triggering apoptosis. These findings pave the way for further investigations into the therapeutic applications of miR-365a-3p in oxidative stress-related liver diseases.
کلمات کلیدیROS, HepG2, Antioxidant proteins, miR-365a-3p

لینک دانلود مقاله
hide/show

نام فایل تاریخ درج فایل اندازه فایل دانلود
Govahi.jpg1403/10/05273039دانلود
The miR-AG-EA2.final.pdf1403/10/05362274دانلود