Adenosine Deaminase Family Acting on RNA 1 (ADAR1) May Be a De Novo Target for Endometriosis Treatment

被引:0
|
作者
Vu, Thuy Ha [1 ]
Nakamura, Keiichiro [1 ,3 ]
Shigeyasu, Kunitoshi [2 ]
Kubo, Kotaro [1 ]
Kashino, Chiaki [1 ]
Masuyama, Hisashi [1 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Obstet & Gynecol, Okayama, Japan
[2] Okayama Univ, Dept Gastroenterol Surg, Grad Sch Med Dent & Pharmaceut Sci, Okayama, Japan
[3] Okayama Univ, Dept Obstet & Gynecol, Grad Sch Med Dent & Pharmaceut Sci, 2-5-1 Shikata Cho,Kita Ku, Okayama, Okayama 7008558, Japan
来源
IN VIVO | 2024年 / 38卷 / 02期
关键词
ADAR1; endometriosis; apoptosis; potential therapeutic target; PROTEIN-KINASE PKR; EDITING ENZYME; PRINCIPLES; MEMBER; GENE;
D O I
10.21873/invivo.13489
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background/Aim: Adenosine deaminase family acting on RNA 1 (ADAR1) expression was examined to determine its correlation with endometriosis. The biological functions and inhibitory effects of ADAR1 knockdown were investigated in a human endometriotic cell line. Materials and Methods: ADAR1 was examined in patients with and without endometriosis using reverse transcription polymerase chain reaction (RT-PCR), and the apoptotic expression of ADAR1 small interfering RNA (siRNA) was confirmed using flow cytometry. The biological functions and inhibitory effects of ADAR1 knockdown were investigated using RT-PCR in a 12Z immortalized human endometriotic cell line. Results: ADAR1 expression was significantly higher in patients with endometriosis than in those without (p<0.001). ADAR1 siRNA increased early and late apoptosis, compared to the mock (24.83%) and control (19.96%) cells. ADAR1 knockdown led to apoptosis through MDA5, RIG -I, IRF3, IRF7, caspase 3, caspase 7, and caspase 8 expression in the cell lines. Conclusion: ADAR1 is a potential novel therapeutic target in endometriosis.
引用
收藏
页码:683 / 690
页数:8
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