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Knockdown of Rap2B, a Ras Superfamily Protein, Inhibits Proliferation, Migration, and Invasion in Cervical Cancer Cells via Regulating the ERK1/2 Signaling Pathway

机译:Rap2B的敲低通过调节ERK1 / 2信号通路抑制宫颈癌细胞中的增殖,迁移和侵袭,抑制宫颈癌细胞中的增殖,迁移和侵袭

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摘要

Rap2B, belonging to the Ras superfamily, has been implicated in cancer development and functions as a tumor promoter. However, the role of Rap2B in cervical cancer is unknown. In this study, we investigated the expression pattern and biological functions of Rap2B in cervical cancer. The results showed that Rap2B was overexpressed in cervical cancer tissues and cell lines. Knockdown of Rap2B inhibited the proliferation, migration, and invasion of cervical cancer cells. In addition, our tumorigenesis assay showed that Rap2B knockdown suppressed cervical cancer cell growth and metastasis in vivo. We also found that the ERK1/2 signaling pathway is involved in the inhibitory effect of Rap2B knockdown on cervical cancer development. In conclusion, we suggest that Rap2B is an oncogene and may be a promising therapeutic target for cervical cancer.
机译:RAP2B属于RAS超家族,已涉及癌症发育和用作肿瘤启动子。 然而,Rap2b在宫颈癌中的作用是未知的。 在这项研究中,我们研究了Rap2b在宫颈癌中的表达模式和生物学功能。 结果表明,RAP2B在宫颈癌组织和细胞系中过表达。 Rap2B的敲低抑制宫颈癌细胞的增殖,迁移和侵袭。 此外,我们的肿瘤发生器测定表明,RAP2B敲低抑制了宫颈癌细胞生长和体内转移。 我们还发现ERK1 / 2信号传导途径参与了RAP2B敲低对宫颈癌发育的抑制作用。 总之,我们表明RAP2B是癌基因,可能是宫颈癌的有希望的治疗靶标。

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