TRAF6 regulates the signaling pathway influencing colorectal cancer function through ubiquitination mechanisms

被引:23
作者
Zhu Guangwei [1 ]
Cheng Zhibin [1 ]
Wang Qin [1 ]
Lin Chunlin [1 ,2 ]
Lin Penghang [1 ,2 ]
He Ruofan [1 ,2 ]
Chen Hui [1 ,2 ]
Hoffman, Robert M. [3 ,4 ]
Ye Jianxin [1 ]
机构
[1] Fujian Med Univ, Hosp 1, Key Lab Accurate Diag & Treatment Canc, Inst Abdominal Surg,Sect 2,Dept Gastrointestinal, 20th Chazhong Rd, Fuzhou 350005, Fujian, Peoples R China
[2] Fujian Med Univ Fuzhou, Key Lab Minist Educ Gastrointestinal Canc, Fuzhou, Peoples R China
[3] AntiCanc Inc, San Diego, CA USA
[4] Univ Calif San Diego, Dept Surg, San Diego, CA 92103 USA
基金
中国国家自然科学基金;
关键词
colorectal cancer; lymphangiogenesis; NF-kappa B; TRAF6; ubiquitination; GROWTH-FACTOR RECEPTOR-3; KAPPA-B; TNF RECEPTOR; COLON-CANCER; PROMOTES; TUMOR; LYMPHANGIOGENESIS; METASTASIS; INVASION; LPS;
D O I
10.1111/cas.15302
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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-kappa B-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-kappa B-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.
引用
收藏
页码:1393 / 1405
页数:13
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