Your browser doesn't support javascript.
loading
節目: 20 | 50 | 100
结果 1 - 2 de 2
过滤器
添加過濾器








年份範圍
1.
Chinese Medical Journal ; (24): 447-455, 2022.
文章 在 英语 | WPRIM | ID: wpr-927548

摘要

BACKGROUND@#Systemic lupus erythematosus (SLE) is a complex autoimmune disease, and the mechanism of SLE is yet to be fully elucidated. The aim of this study was to explore the role of two-pore segment channel 2 (TPCN2) in SLE pathogenesis.@*METHODS@#Quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to detect the expression of TPCN2 in SLE. We performed a loss-of-function assay by lentiviral construct in Jurkat and THP-1 cell. Knockdown of TPCN2 were confirmed at the RNA level by qRT-PCR and protein level by Western blotting. Cell Count Kit-8 and flow cytometry were used to analyze the cell proliferation, apoptosis, and cell cycle of TPCN2-deficient cells. In addition, gene expression profile of TPCN2-deficient cells was analyzed by RNA sequencing (RNA-seq).@*RESULTS@#TPCN2 knockdown with short hairpin RNA (shRNA)-mediated lentiviruses inhibited cell proliferation, and induced apoptosis and cell-cycle arrest of G2/M phase in both Jurkat and THP-1 cells. We analyzed the transcriptome of knockdown-TPCN2-Jurkat cells, and screened the differential genes, which were enriched for the G2/M checkpoint, complement, and interleukin-6-Janus kinase-signal transducer and activator of transcription pathways, as well as changes in levels of forkhead box O, phosphatidylinositol 3-kinase/protein kinase B/mechanistic target of rapamycin, and T cell receptor pathways; moreover, TPCN2 significantly influenced cellular processes and biological regulation.@*CONCLUSION@#TPCN2 might be a potential protective factor against SLE.


Subject(s)
Humans , Apoptosis/genetics , Cell Division , Jurkat Cells , Lupus Erythematosus, Systemic/genetics , RNA, Small Interfering/genetics
2.
文章 在 中文 | WPRIM | ID: wpr-693480

摘要

Long non-coding RNAs (lncRNAs) can promote or inhibit the occurrence and development of pancreatic cancer,lung cancer,gastric cancer and breast cancer by regulating the expression of protein,signal pathway and cell cycle in different ways.Further studies of mechanisms of different lncRNAs in tumors may provide new methods for the diagnosis and treatment of cancers.

搜索明细