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首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >Anxa5 mediates the in vitro malignant behaviours of murine hepatocarcinoma Hca-F cells with high lymph node metastasis potential preferentially via ERK2/p-ERK2/c-Jun/p-c-Jun(Ser73) and E-cadherin
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Anxa5 mediates the in vitro malignant behaviours of murine hepatocarcinoma Hca-F cells with high lymph node metastasis potential preferentially via ERK2/p-ERK2/c-Jun/p-c-Jun(Ser73) and E-cadherin

机译:ANXA5通过ERK2 / P-ERK2 / C-Jun / P-C-Jun(Ser73)和E-Cadherin,用高淋巴结转移潜力介导小淋巴结转移潜力的鼠肝癌HCA-F细胞的体外恶性行为。

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摘要

Objective: Annexin A5 (Anxa5) is associated with the progression of some cancers, while its role and regulation mechanism in tumor lymphatic metastasis is rarely reported. This study aims to investigate the influence of Anxa5 knockdown on the malignant behaviours of murine hepatocarcinoma Hca-F cell line with high lymph node metastatic (LNM) potential and the underlying regulation mechanism.
机译:目的:附着膜蛋白A5(ANXA5)与某些癌症的进展相关,而其在肿瘤淋巴结转移中的作用和调节机制很少。 本研究旨在调查ANXA5敲低对高淋巴结转移(LNM)电位和潜在调节机制的鼠肝癌HCA-F细胞系恶性行为的影响。

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