2018
DOI: 10.3892/etm.2018.7116
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MicroRNA‑494‑3p protects rat cardiomyocytes against septic shock via PTEN

Abstract: The aim of the present study was to investigate the role of microRNA (miR)-494-3p in myocardial injury in patients with septic shock and the underlying mechanism. A total of 22 patients with sepsis and 17 patients with septic shock were included in the present study. In addition, 20 healthy subjects were recruited as the control group. Peripheral blood was collected from all subjects and a rat cardiomyocyte model of myocardial injury was constructed. Reverse transcription-quantitative polymerase chain reaction… Show more

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Cited by 20 publications
(23 citation statements)
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References 43 publications
(42 reference statements)
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“…Previous studies have found that cell apoptosis plays an important role in sepsis-induced myocardial depression [ 6 ], but the mechanism which specifically regulates apoptosis in this context is still unclear. Notably, microRNAs (miRNAs) can regulate cell apoptosis.…”
Section: Introductionmentioning
confidence: 99%
“…Previous studies have found that cell apoptosis plays an important role in sepsis-induced myocardial depression [ 6 ], but the mechanism which specifically regulates apoptosis in this context is still unclear. Notably, microRNAs (miRNAs) can regulate cell apoptosis.…”
Section: Introductionmentioning
confidence: 99%
“…Wu et al found that also miR-494-3p targeted PTEN [ 60 ]. miR-494-3p is down-regulated in septic patients’ blood and its decrease correlates with the cardiac dysfunction.…”
Section: Resultsmentioning
confidence: 99%
“…It is a phosphatase that regulates various cellular signaling pathways and has tumor suppression properties. Some of the aforementioned studies demonstrated that PTEN is targeted by miRNAs in sepsis-induced cardiac damage [ 53 , 59 , 60 ]. A further complication in understanding the role of miRNAs in septic myocardial injury is represented by lncRNAs, as evidenced by some research studies mentioned above [ 45 , 73 , 74 ].…”
Section: Discussionmentioning
confidence: 99%
“…Another important finding in this research reflected that the elevation of miR-494 and knockdown of RIPK1 could accelerate the proliferation of neurons in the hippocampus of rats with Ep. Similarly, miR-494 has been revealed to be reduced in the temporal cortex of patients with mTLE [9], Wu et al have pointed out that the up-regulation of miR-494-3p was able to promote the proliferation in rat cardiomyocytes [30]. As for the effects of silenced RIPK1 in cell proliferation, Zhao et al have demonstrated that the reduction of RIPK1 has the capacity to promote the proliferation of myocardial cells in myocardial ischemia/ reperfusion (I/R) injury [31].…”
Section: Discussionmentioning
confidence: 97%