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Yes-associated protein promotes cell proliferation by activating Fos Related Activator-1 in oral squamous cell carcinoma

机译:是的相关蛋白通过激活口腔鳞状细胞癌中的Fos Related Activator-1促进细胞增殖

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In our previous study, we established an in vitro cellular carcinogenesis model of oral squamous cell carcinoma (OSCC), including a human immortalized oral epithelial cell (HIOEC) and a cancerous cell line (HB96). Microarray analysis showed that the gene encoding Yes-associated protein (YAP) was significantly increased in HB96 cells compared with HIOEC cells. But the underlying mechanism of YAP on oncogenesis, especially its downstream targets, are still not clear. YAP expression in OSCC cell lines and tissue specimens were investigated by using realtime PCR. western blotting and immunohistochem-istry staining. YAP put-back plasmid with four mutation sites after YAP-siRNA interference was constructed by site-directed muugenesis. Cell growth and colony formation were observed after YAP-siRNA interference or YAP put-back again in CAL27 cells. YAP expression was increased in the cellular carcinogenesis models and the clinical samples from primary OSCC patients. Inhibition of YAP by siRNA interference in CAL27 cells significantly inhibited cell proliferation and colony formation in soft agar. but these abilities were rescued when YAP was put-back again. At the same time, Fos Related Activator-1 (Fra-1) was downregulated when YAP was inhibited by siRNA interference while Fra-1 was rescued when YAP was put-back again. Immunohistochemistry results also indicated that higher levels of YAP were significantly associated with Fra-1 overexpression in OSCC clinical samples. YAP could promote cell proliferation by activating transcription factor Fra1 in oral squamous cell carcinoma.
机译:在我们先前的研究中,我们建立了口腔鳞状细胞癌(OSCC)的体外细胞致癌模型,包括人类永生化口腔上皮细胞(HIOEC)和癌细胞系(HB96)。芯片分析表明,与HIOEC细胞相比,HB96细胞中编码Yes相关蛋白(YAP)的基因显着增加。但是,YAP对肿瘤发生的潜在机制,特别是其下游靶点,尚不清楚。通过使用实时PCR研究了OSCC细胞系和组织标本中的YAP表达。免疫印迹和免疫组化染色。通过定点诱变构建YAP-siRNA干扰后具有四个突变位点的YAP回收质粒。在CAL27细胞中,YAP-siRNA干扰或YAP放回后,观察到细胞生长和集落形成。在原发性OSCC患者的细胞癌变模型和临床样品中,YAP表达增加。在CAL27细胞中通过siRNA干扰抑制YAP可显着抑制软琼脂中的细胞增殖和集落形成。但是当再次撤回YAP时,这些能力得以挽救。同时,当siRNA干扰抑制YAP时,Fos Related Activator-1(Fra-1)被下调,而当再次放回YAP时,则拯救了Fra-1。免疫组织化学结果还表明,较高的YAP水平与OSCC临床样品中的Fra-1过表达显着相关。 YAP可以通过激活口腔鳞状细胞癌中的转录因子Fra1来促进细胞增殖。

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