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Kaempferia parviflora Extract Inhibits STAT3 Activation and Interleukin-6 Production in HeLa Cervical Cancer Cells

机译:山竹(Kaempferia parviflora)提取物抑制Hela宫颈癌细胞中的STAT3活化和白介素6的产生

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摘要

Kaempferia parviflora (KP) has been reported to have anti-cancer activities. We previously reported its effects against cervical cancer cells and continued to elucidate the effects of KP on inhibiting the production and secretion of interleukin (IL)-6, as well as its relevant signaling pathways involved in cervical tumorigenesis. We discovered that KP suppressed epidermal growth factor (EGF)-induced IL-6 secretion in HeLa cells, and it was associated with a reduced level of Glycoprotein 130 (GP130), phosphorylated signal transducers and activators of transcription 3 (STAT3), and Mcl-1. Our data clearly showed that KP has no effect on nuclear factor kappa B (NF-κB) localization status. However, we found that KP inhibited EGF-stimulated phosphorylation of tyrosine 1045 and tyrosine 1068 of EGF receptor (EGFR) without affecting its expression level. The inhibition of EGFR activation was verified by the observation that KP significantly suppressed a major downstream MAP kinase, ERK1/2. Consistently, KP reduced the expression of Ki-67 protein, which is a cellular marker for proliferation. Moreover, KP potently inhibited phosphorylation of STAT3, Akt, and the expression of Mcl-1 in response to exogenous IL-6 stimulation. These data suggest that KP suppresses EGF-induced production of IL-6 and inhibits its autocrine IL-6/STAT3 signaling critical for maintaining cancer cell progression. We believe that KP may be a potential alternative anti-cancer agent for suppressing cervical tumorigenesis.
机译:据报道,Kaempferia parviflora(KP)具有抗癌活性。我们先前报道了其对子宫颈癌细胞的作用,并继续阐明了KP对抑制白介素(IL)-6的产生和分泌及其与子宫颈肿瘤发生有关的信号通路的影响。我们发现KP抑制HeLa细胞中表皮生长因子(EGF)诱导的IL-6分泌,并且它与糖蛋白130(GP130),磷酸化信号转导子和转录激活因子3(STAT3)和Mcl的水平降低有关-1。我们的数据清楚地表明,KP对核因子κB(NF-κB)的定位状态没有影响。但是,我们发现KP抑制EGF刺激的EGF受体(EGFR)的酪氨酸1045和酪氨酸1068的磷酸化,而不影响其表达水平。通过观察到KP显着抑制了主要的下游MAP激酶ERK1 / 2,证实了对EGFR激活的抑制作用。一致地,KP减少了Ki-67蛋白的表达,该蛋白是增殖的细胞标记。此外,KP可以有效抑制STAT3,Akt的磷酸化以及响应外源IL-6刺激的Mcl-1的表达。这些数据表明,KP抑制EGF诱导的IL-6产生并抑制其自分泌IL-6 / STAT3信号,这对于维持癌细胞的进展至关重要。我们认为,KP可能是抑制宫颈肿瘤发生的潜在替代抗癌药。

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