scholarly journals Long Noncoding RNA-Maternally Expressed Gene 3 Contributes to Hypoxic Pulmonary Hypertension

Author(s):  
Yan Xing ◽  
Xiaodong Zheng ◽  
Yao Fu ◽  
Jing Qi ◽  
Minghui Li ◽  
...  
2019 ◽  
Vol 27 (12) ◽  
pp. 2166-2181 ◽  
Author(s):  
Yan Xing ◽  
Xiaodong Zheng ◽  
Yao Fu ◽  
Jing Qi ◽  
Minghui Li ◽  
...  

2018 ◽  
Author(s):  
Yan Xing ◽  
Xiaodong Zheng ◽  
Yao Fu ◽  
Jing Qi ◽  
Minghui Li ◽  
...  

ABSTRACTThe expression and function of long noncoding RNAs (lncRNAs) in the development of hypoxic pulmonary hypertension, especially in the proliferation of pulmonary artery smooth muscle cells (PASMCs) are largely unknown. Here, we characterized the expression of lncRNA-maternally expressed gene 3 (lncRNA-MEG3) was significantly increased and primarily located in the cytoplasm of PASMCs by hypoxia. LncRNA-MEG3 knockdown by lung-specific delivery of small interfering RNAs (siRNAs) significantly prevented the development of hypoxic pulmonary hypertension in vivo. Silencing of lncRNA-MEG3 by siRNAs and gapmers attenuated PASMC responses to hypoxia in vitro. Mechanically, we found that lncRNA-MEG3 acts as a molecular sponge of microRNA-328 (miR-328); upon hypoxia, lncRNA-MEG3 interacts and sequesters miR-328, leading to the upregulation of insulin-like growth factor 1 receptor (IGF1R). Additionally, higher expression of lncRNA-MEG3 and IGF1R, and lower expression of miR-328 were observed in PASMCs of iPAH patients. These data provide insight into the contribution of lncRNA-MEG3 in hypoxia pulmonary hypertension. Upregulation of lncRNA-MEG3 sequesters cytoplasmic miR-328, eventually leading to the expression of IGF1R, revealing a regulatory mechanism by lncRNAs in hypoxia-induced PASMC proliferation.


Gene ◽  
2016 ◽  
Vol 579 (1) ◽  
pp. 23-28 ◽  
Author(s):  
Xiaohua Wang ◽  
Chao Yan ◽  
Xiaoling Xu ◽  
Liangliang Dong ◽  
Hua Su ◽  
...  

2016 ◽  
Vol 35 (4) ◽  
pp. S358 ◽  
Author(s):  
M. Brock ◽  
C. Schuoler ◽  
S. Ulrich ◽  
R. Speich ◽  
M. Gassmann ◽  
...  

2020 ◽  
Vol 202 (10) ◽  
pp. 1445-1457 ◽  
Author(s):  
Christoph M. Zehendner ◽  
Chanil Valasarajan ◽  
Astrid Werner ◽  
Jes-Niels Boeckel ◽  
Florian C. Bischoff ◽  
...  

2020 ◽  
Vol 19 ◽  
pp. 153303382094581
Author(s):  
Chunling He ◽  
Xinmei Wang ◽  
Jing Luo ◽  
Yinghua Ma ◽  
Zhen Yang

Objective: Our study aimed to investigate the correlation of long noncoding RNA maternally expressed gene 3 expression with clinical features, treatment response, and survival profiles in patients with acute myeloid leukemia. Methods: Bone marrow samples of 122 de novo patients with acute myeloid leukemia (prior to treatment) and 30 healthy donors (after enrollment) were collected, and long noncoding RNA maternally expressed gene 3 expression was detected by reverse transcription quantitative polymerase chain reaction. According to median value of long noncoding RNA maternally expressed gene 3 expression in patients with acute myeloid leukemia, they were divided into long noncoding RNA maternally expressed gene 3 high expression and low expression patients (which were further categorized as low---, low--, and low- expression patients). Results: Long noncoding RNA maternally expressed gene 3 expression was decreased in patients with acute myeloid leukemia compared to healthy donors. Besides, receiver operating characteristic curve displayed that long noncoding RNA maternally expressed gene 3 distinguished patients with acute myeloid leukemia from healthy donors. In patients with acute myeloid leukemia, long noncoding RNA maternally expressed gene 3 low expression was associated with poor-risk stratification but was not correlated with age, gender, French-American-Britain classification, or white blood cell level. For prognosis, complete remission rate was lowest in long noncoding RNA maternally expressed gene 3 low--- expression patients, followed by long noncoding RNA maternally expressed gene 3 low-- expression patients, long noncoding RNA maternally expressed gene 3 low- expression patients, and was highest in long noncoding RNA maternally expressed gene 3 high expression patients; Kaplan-Meier curves displayed that lower long noncoding RNA maternally expressed gene 3 expression was associated with reduced event-free survival and overall survival; Cox regression analysis showed that lower long noncoding RNA maternally expressed gene 3 expression independently predicted decreased event-free survival and worse overall survival in patients with acute myeloid leukemia. Conclusion: Long noncoding RNA maternally expressed gene 3 may function as a novel marker for effective surveillance and management of acute myeloid leukemia.


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