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Transcriptional factor OCT4 promotes esophageal cancer metastasis by inducing epithelial-mesenchymal transition through VEGF-C/VEGFR-3 signaling pathway

机译:转录因子OCT4通过通过VEGF-C / VEGFR-3信号途径诱导上皮-间质转化来促进食道癌转移

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摘要

The octamer-binding transcription factor 4 (OCT4) can promote cancer proliferation and metastasis. Esophageal carcinoma (ECC) harbors different quantities of OCT4-positive cancer cells. These cells are highly malignant and prone to metastasis; however, the mechanism remains unknown. In this study, we found that OCT4 enhances vascular endothelial growth factor C (VEGF-C) promoter activity to promote VEGF-C expression and activates VEGF receptor 3 (VEGFR-3) in ECC cells, thereby inducing cancer cell epithelial-mesenchymal transition (EMT). Studies using xenograft models showed that OCT4 promoted xenograft growth and intraperitoneal implantation metastasis of ECC cells. Downregulation of OCT4 expression could inhibit cancer metastasis. OCT4- and VEGF-C-positive ECC presented more malignant biological behaviors and the corresponding patients exhibited a poor prognosis. The study confirmed that the OCT4/VEGF-C/VEGFR-3/EMT signaling plays a role in the progression of ECC. Understanding of how OCT4 regulates EMT and how ECC metastasis occurs will provide useful targets for the biological treatment of ECC.
机译:八聚物结合转录因子4(OCT4)可以促进癌症的扩散和转移。食道癌(ECC)包含不同数量的OCT4阳性癌细胞。这些细胞是高度恶性的,易于转移。但是,该机制仍然未知。在这项研究中,我们发现OCT4增强了ECC细胞中的血管内皮生长因子C(VEGF-C)启动子活性以促进VEGF-C表达并激活VEGF受体3(VEGFR-3),从而诱导癌细胞上皮-间质转化( EMT)。使用异种移植模型的研究表明,OCT4促进了ECC细胞的异种移植生长和腹膜内植入转移。 OCT4表达的下调可以抑制癌症转移。 OCT4和VEGF-C阳性ECC表现出更多的恶性生物学行为,相应的患者预后较差。研究证实,OCT4 / VEGF-C / VEGFR-3 / EMT信号传导在ECC的进展中起作用。了解OCT4如何调节EMT以及ECC转移如何发生将为ECC的生物学治疗提供有用的靶标。

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