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Expression and subcellular distribution of Bcl-2 and BAX proteins in serum-starved human keratinocytes and mouth carcinoma epidermoid cultures.

机译:Bcl-2和BAX蛋白在血清饥饿的人角质形成细胞和口腔癌表皮样培养物中的表达和亚细胞分布。

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Squamous cell carcinoma (SSC) is the most frequent malignant tumor of the oral cavity. Aberration of programmed cell death is thought to participate in cancer. Using specific antibodies a study of the expression and subcellular distribution of Bcl-2, BAX, caspase-3 and cytochrome c in normal human keratinocytes and mouth carcinoma slowly (HN) and rapidly growing (KB) cells has been carried out. In carcinoma cells depressed expression of BAX, presence in the cytosol of procaspase-3 and absence in this fraction of cytochrome c have been found. PGE2 treatment prevented cell growth depression induced by pro-apoptotic serum starvation both in control and carcinoma cell cultures. It is also shown that PGE2 promoted both in keratinocytes and KB cells expression of Bcl-2, which was accompanied in the first case by increase in its mitochondrial level. These results indicate that in carcinoma cells there is an apparent down regulation of the apoptotic cascade as compared to normal keratinocytes. Thus the possibility that down regulation of apoptosis is associated with promotion of tumor development in the oral mucosa cells seems to be supported by these observations.
机译:鳞状细胞癌(SSC)是口腔中最常见的恶性肿瘤。程序性细胞死亡的异常被认为与癌症有关。使用特异性抗体研究了Bcl-2,BAX,caspase-3和细胞色素c在正常人角质形成细胞和口腔癌中缓慢表达(HN)和快速生长(KB)的表达和亚细胞分布。在癌细胞中抑制了BAX表达的细胞中,发现procaspase-3存在于细胞溶胶中,而这部分细胞色素c则不存在。 PGE 2处理可防止在对照和癌细胞培养中由促凋亡血清饥饿引起的细胞生长抑制。还显示PGE 2促进了Bcl-2在角质形成细胞和KB细胞中的表达,这在第一种情况下伴随着其线粒体水平的增加。这些结果表明,与正常的角质形成细胞相比,在癌细胞中凋亡级联的明显下调。因此,这些观察结果似乎支持了凋亡下调与促进口腔粘膜细胞内肿瘤发展相关的可能性。

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