دورية أكاديمية

Regulation mechanism and pathogenic role of lncRNA plasmacytoma variant translocation 1 (PVT1) in human diseases

التفاصيل البيبلوغرافية
العنوان: Regulation mechanism and pathogenic role of lncRNA plasmacytoma variant translocation 1 (PVT1) in human diseases
المؤلفون: Fang Wu, Yiping Zhu, Caiping Zhou, Weiwei Gui, Hong Li, Xihua Lin
المصدر: Genes and Diseases, Vol 10, Iss 3, Pp 901-914 (2023)
بيانات النشر: KeAi Communications Co., Ltd., 2023.
سنة النشر: 2023
المجموعة: LCC:Medicine (General)
LCC:Genetics
مصطلحات موضوعية: Cancer, ceRNA, CircPVT1, Long non-coding RNAs, MicroRNAs, MYC, Medicine (General), R5-920, Genetics, QH426-470
الوصف: Plasmacytoma variant translocation 1 (PVT1) is a long non-coding RNA (lncRNA) gene identified as a recurrent breakpoint of Burkitt’s lymphomas. Human PVT1 gene is located on region 8q24.21, a well-known cancer risk region, and encodes at least 26 linear ncRNA isoforms and 26 circular RNA isoforms, as well as 6 microRNAs. Several PVT1 functioning models have been reported recently such as competing endogenous RNA (ceRNA) activity and regulating protein stability of oncogenes, especially MYC oncogene. The promoter of PVT1 gene is a boundary element of tumor-suppressor DNA. CircPVT1 derived from PVT1 gene is also a critical non-coding oncogenic RNA. Although substantial advancements have been made in understanding the roles of PVT1 in cancer recently, the detailed mechanisms underlying its functions remain unclear. Herein, we summarize the recent progressions on the mechanisms underlying PVT1 regulated gene expression at different levels. We also discuss the interaction between lncRNA and protein, RNA and DNA, as well as the potential cancer therapy strategy by targeting these networks.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2352-3042
Relation: http://www.sciencedirect.com/science/article/pii/S2352304222001726; https://doaj.org/toc/2352-3042
DOI: 10.1016/j.gendis.2022.05.037
URL الوصول: https://doaj.org/article/edc3439b65364fd29bca44370d6801b6
رقم الأكسشن: edsdoj.3439b65364fd29bca44370d6801b6
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:23523042
DOI:10.1016/j.gendis.2022.05.037