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Krüppel-like Factor 5 Promotes Sonic Hedgehog Signaling and Neoplasia in Barrett's Esophagus and Esophageal Adenocarcinoma

机译:克虏伯样因子5促进巴雷特食管和食管腺癌中的声波刺猬信号和肿瘤形成。

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Krüppel-like Factor 5 (KLF5) is a zinc-finger transcription factor associated with cell cycle progression and cell survival. KLF5 plays a key role in mammalian intestinal epithelium development and maintenance, expressed at high levels in basal proliferating cells and low levels in terminally differentiated cells. Considering Barrett's esophagus (BE) and esophageal adenocarcinoma's (EAC) histopathological similarities to intestinal epithelium, we sought to determine KLF5’s role in BE and EAC, as well as KLF5’s possible connection to the sonic hedgehog (SHH) pathway which is highly active in BE and EAC development. Low levels of KLF5 mRNA were found in BE cell lines and tissue– similar to what has been reported in differentiated intestinal epithelium. In contrast, higher KLF5 levels were observed in EAC cells and tissues. KLF5 knockdown in EAC cells caused significant decreases in cell migration, proliferation, and EAC-associated gene expression. Moreover, KLF5 knockdown led to decreased SHH signaling. These results suggest that KLF5 is connected to the SHH pathway in BE and EAC and may represent a potential drug target in EAC; further studies are now indicated to verify these findings and elucidate underlying mechanisms involved.
机译:Krüppel样因子5(KLF5)是与细胞周期进程和细胞存活相关的锌指转录因子。 KLF5在哺乳动物肠道上皮的发育和维持中起关键作用,在基底增殖细胞中高水平表达,而在终末分化细胞中低水平表达。考虑到Barrett食道(BE)和食道腺癌(EAC)与肠上皮的组织病理学相似性,我们试图确定KLF5在BE和EAC中的作用,以及KLF5可能与在BE和EAC中活跃的声波刺猬(SHH)途径有关。 EAC开发。在BE细胞系和组织中发现低水平的KLF5 mRNA,这与分化的肠上皮细胞中报道的相似。相反,在EAC细胞和组织中观察到较高的KLF5水平。 EAC细胞中的KLF5敲低导致细胞迁移,增殖和EAC相关基因表达显着下降。此外,KLF5敲低导致减少SHH信号。这些结果表明,KLF5与BE和EAC中的SHH途径相关,并且可能代表EAC中的潜在药物靶标。现在需要进行进一步的研究以验证这些发现并阐明涉及的潜在机制。

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