| Literature DB >> 31036380 |
Yali Wang1, Yitong Yuan1, Yuantao Gao2, Xiao Li1, Feng Tian1, Fang Liu1, Ruochen Du1, Pengfei Li1, Fei Wang1, Suming Xu3, Xueqing Wu4, Chunfang Wang5.
Abstract
Apoptosis is a highly conservative energy demand program for non-inflammatory cell death, which is extremely significant in normal physiology and disease. There are many techniques used for studying apoptosis. MicroRNA (miRNA) is closely related to cell apoptosis, and especially microRNA-31 (miR-31) is involved in apoptosis by regulating a large number of target genes and signaling pathways. In many neurological diseases, cell apoptosis or programmed cell death plays an important role in the reduction of cell number, including the reduction of neurons in spinal cord injuries. In recent years, the phosphoinositol 3-kinase/AKT (PI3K/AKT) signal pathway, as a signal pathway involved in a variety of cell functions, has been studied in spinal cord injury diseases. The PI3K/AKT pathway directly or indirectly affects whether apoptosis occurs in a cell, thereby affecting a significant intracellular event sequence. This paper reviewed the interactions of miR-31 target sites in the PI3K/AKT signaling pathway, and explored new ways to prevent and treat spinal cord injury by regulating the effect of miR-31 on apoptosis.Entities:
Keywords: Apoptosis; MicroRNA; MicroRNA-31; PI3K/AKT signaling pathway; Spinal cord injury
Year: 2019 PMID: 31036380 DOI: 10.1016/j.braindev.2019.04.010
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961