首页> 美国卫生研究院文献>Toxicology Reports >Areca nut extracts exert different effects in oral cancer cells depending on serum concentration: A clue to the various oral alterations in betel quid chewers
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Areca nut extracts exert different effects in oral cancer cells depending on serum concentration: A clue to the various oral alterations in betel quid chewers

机译:槟榔提取物在口腔癌细胞中的作用取决于血清浓度:槟榔咀嚼物的各种口腔变化的线索

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摘要

Betel quid chewing is associated with various pathologic alterations in oral mucosa. However, the molecular mechanism behind so many contradictory alterations remains unclear. Here we aimed to build a model to facilitate the related studies in cultured cells. In our results, areca nut extract (ANE) was found to exert different effects in oral cells depending on the supplemented serum level. ANE strongly induced DNA damage, necrotic ballooning, and inflammatory cytokines under lower serum concentration while might convert to facilitate deregulated growth of serum-supplemented cells via modulating the activity/expression of factors such as E-cadherin and Snail. Despite ANE significantly activated NF-κB, a mediator critical for inflammation, inhibition of NF-κB did not prevent the activation of IL8 promoter. We further discovered Y705-dephosphorylated STAT3 might enhance IL8 transcription. Since necrosis and the inflammatory cytokines could cause massive inflammation, infiltration of interstitial fluid might potentiate cellular resistance against the acute cytotoxicity of ANE and further support the proliferation of transforming cells. Induction of VEGF and angiogenesis under lower serum condition also paved the way for cell growth and subsequent metastasis. Accordingly, we concluded that in correlation with serum infiltration ANE caused particular effects in oral cells and possibly the various clinicopathological alterations in vivo.
机译:槟榔咀嚼与口腔粘膜的各种病理改变有关。然而,如此多矛盾的改变背后的分子机制仍然不清楚。在这里,我们旨在建立一个模型来促进培养细胞的相关研究。在我们的结果中,发现槟榔提取物(ANE)在口腔细胞中的作用取决于补充的血清水平。 ANE在较低的血清浓度下会强烈诱导DNA损伤,坏死性球囊扩张和炎性细胞因子,同时可能通过调节E-钙黏着蛋白和Snail等因子的活性/表达而转变为促进补充血清的细胞生长失调。尽管ANE能够显着激活NF-κB(炎症的关键介质),但抑制NF-κB并不能阻止IL8启动子的激活。我们进一步发现Y705去磷酸化STAT3可能增强IL8转录。由于坏死和炎性细胞因子可能引起大量炎症,因此间质液的浸润可能增强细胞对ANE急性细胞毒性的抵抗力,并进一步支持转化细胞的增殖。在较低血清条件下诱导VEGF和血管生成也为细胞生长和随后的转移铺平了道路。因此,我们得出结论,与血清浸润相关,ANE在口腔细胞中可能引起特殊作用,并可能在体内引起各种临床病理改变。

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