2016
DOI: 10.1016/j.neulet.2015.11.050
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siRNA mediated down-regulation of Sprouty2/4 diminishes ischemic brain injury

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Cited by 9 publications
(6 citation statements)
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“…This gene has also been suggested as a possible pharmacological target for stroke patients 70 , as it promotes angiogenesis and glial scarring around the ischemic injury, and therefore prevents increase in lesion size and secondary damage to brain tissue. 71 In addition, SPRY2 may exert neuroprotective effects as its expression regulates BDNF-induced signaling pathways 72 . Similarly, PIKFYVE is an important regulator of platelet lysosome homeostasis 73 , which in turn may promote recovery after ischemic stroke 74 .…”
Section: Discussionmentioning
confidence: 99%
“…This gene has also been suggested as a possible pharmacological target for stroke patients 70 , as it promotes angiogenesis and glial scarring around the ischemic injury, and therefore prevents increase in lesion size and secondary damage to brain tissue. 71 In addition, SPRY2 may exert neuroprotective effects as its expression regulates BDNF-induced signaling pathways 72 . Similarly, PIKFYVE is an important regulator of platelet lysosome homeostasis 73 , which in turn may promote recovery after ischemic stroke 74 .…”
Section: Discussionmentioning
confidence: 99%
“…Consistent with our findings, Klimaschewski et al reported that downregulation of SPRY2 in mice conferred neuroprotective effects and induced injury-induced astrogliosis which limited neuronal cell death and lesion size. 16 Moreover, we also found that E2F1-downregulated miR-122 and disrupted the MAPK pathway in IS via SPRY2. A prior study revealed that E2F1 depletion increased enrichment of MAPK pathway in esophageal squamous cell carcinoma cells.…”
Section: Discussionmentioning
confidence: 56%
“… 15 SPRY2 silencing resulted in reduction of ischemic brain injury through limiting neuronal cell death and lesion size. 16 On basis of this ground, a hypothesis could be proposed that E2F1 might be involved in IS by mediating SPRY2 via miR-122. Therefore, experiments were conducted in clinical, cell, and animal levels to confirm this hypothesis, thus exploring the novel mechanism for IS treatment.…”
Section: Introductionmentioning
confidence: 99%
“…In line with our findings, results from Taniguchi et al implied that Spry4 deficiency accelerated neovascularization and subsequently prevented ischemic injury of hind limb and soft tissue [ 49 ]. Meanwhile, Spry4 knockdown significantly enhanced neuronal survival and functional recovery [ 50 ]. The lung is composed of various cell types, and alveolar epithelial cells (AECs) are the main cell population in the lung.…”
Section: Discussionmentioning
confidence: 99%