IndraLab

Statements



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"Promoter Methylation Analysis Reveals that KCNA5 Ion Channel Silencing Supports Ewing Sarcoma Cell Proliferation."

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"For instance, the phosphorylation of Kv1.5 inhibited the glial proliferation and retarded scar repair ( Perez-Garcia et al., 2018 ), the enhanced expressions of Kv1.3 could control cell proliferation [MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

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"The EdU assay and CCK-8 assay results consistently indicated that KCNA5 silence significantly promoted GC proliferation ( Fig. 3 G–I)."

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"Polycystic ovary syndrome suppresses KCNA5 expression in granulosa cells, slowing down the proliferation of granulosa (Gao et al. 2020)."

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"In response to chronic hypoxia, hypoxia-inducible fact 1-alpha (HIF1-α) and nuclear factor of activated T-cells (NFAT) are overexpressed causing reduced expression and function of Kv1.5 and thereby stimulating PASMC hypertrophy and cell proliferation [3,88,89,90]."

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"In vitro , miRNA153 increased the level of Kv1.5 in hypoxic PASMCs by targeting NFATc3 and inhibiting their proliferation and apoptosis resistance."

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"Here, we observed that KCNA5 was downregulated in GC from PCOS, and KCNA5 suppressed GC proliferation."

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"We explored the effects of Kv1.5 silencing on proliferation and growth of osteosarcoma cells using CCK-8 and colony formation assays, and we found that Kv1.5 silencing significantly suppressed cell proliferation and growth after a 48-h treatment compared to the control-shRNA or untreated groups in MG-63 cells."

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"Consistent with our findings, KCNA5 was reported to suppress proliferation in HEK293 cells [ 29 ]."

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"Silencing Kv1.5 expression significantly inhibited proliferation and induced cell cycle arrest at the G0/G1 phase in osteosarcoma [29] but supported Ewing sarcoma cell proliferation [30]."

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"The knock-out of Kv1.5 in microglia reduces the production of NO and proliferation post-inflammatory insult (Pannasch et al., 2006) through ERK/MAPK pathway, suggesting the proinflammatory role of this outward potassium channel in multiple microglial functions."

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"Specifically, these studies have demonstrated that DNA hypermethylation contributes to epigenetic repression of the KCNA5 locus, and that the consequent suppression of the Kv1.5 ion channel promotes cancer cell proliferation [21]."