核孔蛋白
转移
癌症研究
肝细胞癌
核运输
连环素
核孔
生物
基因敲除
细胞生长
癌变
医学
癌症
Wnt信号通路
细胞质
细胞核
细胞生物学
内科学
信号转导
细胞凋亡
生物化学
遗传学
作者
Censhan Lin,Yuyi Liang,Shu-Guang Su,Yinli Zheng,Xia Yang,Neng Jiang,Lingyi Fu,Jing Zhou,Ying Zhang,Ruijie Deng,Chunhua Wang,Shi-Xun Lu,Yuhua Huang,Li‐Li Liu,Chao Zhang,Jing‐Ping Yun
标识
DOI:10.1016/j.canlet.2021.11.001
摘要
Nuclear pore complex (NPC) embedded in the nuclear envelope, is the only channel for macromolecule nucleocytoplasmic transportation and has important biological functions. However, the deregulation of specific nucleoporins (Nups) and NPC-Nup-based mechanisms and their function in tumour progression remain poorly understood. Here, we aimed to identify the Nups that contribute to HCC progression and metastasis in 729 primary hepatocellular carcinoma (HCC) cases using molecular, cytological, and biochemical techniques. Our results revealed elevated Nup93 expression in HCC tissues, especially in cases with metastasis, and was linked to worse prognosis. Furthermore, Nup93 knockdown suppressed HCC cell metastasis and proliferation, while Nup93 overexpression promoted these activities. We observed that Nup93 promotes HCC metastasis and proliferation by regulating β-catenin translocation. In addition, we found that Nup93 interacted with β-catenin directly, independent of importin. Furthermore, LEF1 and β-catenin facilitated the Nup93-mediated metastasis and proliferation in HCC via a positive feedback loop. Thus, our findings provide novel insights into the mechanisms underlying the Nup93-induced promotion of HCC metastasis and suggest potential therapeutic targets in the LEF1-Nup93-β-catenin pathway for HCC therapeutics.
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