| Literature DB >> 32763292 |
Forough Taheri1, Seyed Omar Ebrahimi2, Salar Shareef3, Somayeh Reiisi4.
Abstract
miRNAs are a class of non-coding RNAs and very conserve molecules that negatively regulate the expression of many genes by targeting the 3' UTR of mRNAs. miRNAs are involved in the modulation of T-cell biology during the earliest and last stages and key controllers of T-cell differentiation and function. The miR-34a, as a major hub of the regulatory network of T cells, plays an important role in T cell activation. miR-34a is widely expressed in immune cells (dendritic cells, macrophages, mast cells, B cells, and T cells) and regulates their development, function, and survival. This miRNA, by targeting over 30 genes across different cellular pathways controls immune response. miR-34a expression is controlled by p53 in transcription level. As well as, miR-34a by activating dendritic cells mediates innate immune response and increases tumor-infiltrating CD8 expression T lymphocytes. In various types of cancers and autoimmune diseases, miR-34a can regulate T cell function and become a possible significant target of microRNA-based therapy. Therefore, in this review, we focus on miR-34a-related regulatory mechanisms in T cell function and understanding mechanisms and molecules involved in this network.Entities:
Keywords: Immune response; Regulatory; T cell; miR-34a
Mesh:
Substances:
Year: 2020 PMID: 32763292 DOI: 10.1016/j.lfs.2020.118209
Source DB: PubMed Journal: Life Sci ISSN: 0024-3205 Impact factor: 5.037