Academic Journal

CircERBB2IP promotes post-infarction revascularization via the miR-145a-5p/Smad5 axis

التفاصيل البيبلوغرافية
العنوان: CircERBB2IP promotes post-infarction revascularization via the miR-145a-5p/Smad5 axis
المؤلفون: Xianping Long, Zhimei Qiu, Chaofu Li, Yan Wang, Jiao Li, Ranzun Zhao, Jidong Rong, Ning Gu, Jinson Yuan, Junbo Ge, Bei Shi
المصدر: Molecular Therapy: Nucleic Acids, Vol 28, Iss , Pp 573-586 (2022)
بيانات النشر: Elsevier, 2022.
سنة النشر: 2022
المجموعة: LCC:Therapeutics. Pharmacology
مصطلحات موضوعية: non-coding RNAs, CircERBB2IP, angiogenesis, miR-145a-5p, GATA4, Smad5, Therapeutics. Pharmacology, RM1-950
الوصف: Myocardial infarction is one of the leading diseases causing death and disability worldwide, and the revascularization of damaged tissues is essential for myocardial-injury repair. Circular RNAs (circRNAs) are widely involved in physiological and pathological processes in various systems throughout the body, and the role of circRNAs in cardiovascular disease is gaining attention. In this study, we determined that circERBB2IP is highly expressed in the hearts of newborn mice. Silencing or overexpression of circERBB2IP inhibited and promoted angiogenesis in vivo and in vitro, respectively. Mechanistically, the transcription factor GATA4 promotes the production of circERBB2IP. Furthermore, circERBB2IP functioned as an endogenous miR-145a-5p sponge and was able to sequester and repress miR-145a-5p activity, which led to an increased expression level of Smad5. In summary, circERBB2IP can promote angiogenesis after myocardial infarction through the miR-145a-5p/Smad5 axis. These data suggest that circERBB2IP may be a potential therapeutic target for the treatment of myocardial infarction.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2162-2531
Relation: http://www.sciencedirect.com/science/article/pii/S2162253122000828; https://doaj.org/toc/2162-2531
DOI: 10.1016/j.omtn.2022.04.006
URL الوصول: https://doaj.org/article/04027c2043c847f285a28fbbd537c8fb
رقم الانضمام: edsdoj.04027c2043c847f285a28fbbd537c8fb
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:21622531
DOI:10.1016/j.omtn.2022.04.006