蛋白激酶B
PI3K/AKT/mTOR通路
细胞凋亡
程序性细胞死亡
细胞生物学
信号转导
激酶
生物
小RNA
癌症研究
生物化学
基因
作者
Yali Wang,Yitong Yuan,Yuantao Gao,Xiao Li,Feng Tian,Fang Liu,Ruochen Du,Pengfei Li,Fei Wang,Suming Xu,Xueqing Wu,Chunfang Wang
标识
DOI:10.1016/j.braindev.2019.04.010
摘要
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.
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