泛素
泛素连接酶
结直肠癌
转移
癌症研究
淋巴管新生
信号转导
医学
癌症
肿瘤坏死因子α
NF-κB
内科学
生物
细胞生物学
生物化学
基因
作者
Guangwei Zhu,Zhibin Cheng,Qin Wang,Chunlin Lin,Penghang Lin,Ruofan He,Hui Chen,Robert M. Hoffman,Jianxin Ye
出处
期刊:Cancer Science
[Wiley]
日期:2022-03-01
卷期号:113 (4): 1393-1405
被引量:9
摘要
Tumor necrosis factor receptor-associated factor-6 (TRAF6) is a ubiquitin E3 ligase. TRAF6 plays an important role in tumor invasion and metastasis. However, the specific mechanism by which TRAF6 promotes colorectal cancer (CRC) metastasis is incompletely understood. This study aimed to determine whether TRAF6 affects the LPS-NF-κB-VEGF-C signaling pathway through ubiquitination, which plays a role in colorectal cancer metastasis. Here, our results showed that TRAF6 affected lymphangiogenesis through the LPS-NF-κB-VEGF-C signaling pathway. Using ubiquitination experiments, we found that TRAF6 was mainly ubiquitinated with the K63-linked chains, and LPS promoted ubiquitination of TRAF6 and K63-linked chains. More importantly, TRAF6 124mut is the main ubiquitination site of TRAF6 interacting with K63-linked chains. TRAF6 affected the migration, invasion, and lymphatic metastasis of colorectal cancer through its ubiquitination. In subcutaneous xenograft models, TRAF6 124mut inhibited tumor growth. In conclusion, our results provide new insight for studying the mechanism of lymphangiogenesis in colorectal cancer to promote cancer metastasis, which may provide new ideas for tumor immunotherapy.
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