State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Department of Pathology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
J Genet Genomics. 2019 Oct 20;46(10):477-488. doi: 10.1016/j.jgg.2019.10.004. Epub 2019 Nov 14.
Ras-association (RA) domain family number 6 (RASSF6) is a member of the Ras-association domain protein family. It is epigenetically inactive and negatively regulates the malignant progression of some tumors. However, its precise role in esophageal squamous cell carcinoma (ESCC) has not been reported. In this study, we performed immunohistochemistry (IHC) assay. The results show that RASSF6 is upregulated in ESCC and that the elevated expression level of RASSF6 is associated with lymph node metastasis and poor survival of ESCC patients. Consistent with the clinical observations, the upregulation of RASSF6 greatly promotes ESCC cell proliferation, migration and invasion as well as the cell cycle transition to G1/S phase in vitro. According to models in vivo, the downregulation of RASSF6 considerably inhibits ESCC tumor growth and lung metastasis. Mechanistically, RASSF6 negatively regulates the tumor suppressor tripartite-motif-containing protein 16 (TRIM16) by promoting its ubiquitination-dependent degradation and eventually activates pathways associated with the cell cycle and epithelial-mesenchymal transition (EMT). Together, these results indicate that the RASSF6-TRIM16 axis is a key effector in ESCC progression and that RASSF6 serves as a potential target for the treatment of ESCC.
Ras 结合(RA)域家族成员 6(RASSF6)是 Ras 结合域蛋白家族的成员。它是表观遗传失活的,可负向调节某些肿瘤的恶性进展。然而,其在食管鳞状细胞癌(ESCC)中的确切作用尚未报道。在本研究中,我们进行了免疫组织化学(IHC)检测。结果表明,RASSF6 在 ESCC 中上调,并且 RASSF6 的高表达水平与 ESCC 患者的淋巴结转移和不良生存相关。与临床观察一致,RASSF6 的上调极大地促进了 ESCC 细胞的增殖、迁移和侵袭以及细胞周期向 G1/S 期的转变。根据体内模型,RASSF6 的下调可显著抑制 ESCC 肿瘤生长和肺转移。在机制上,RASSF6 通过促进其三肽基结构域蛋白 16(TRIM16)的泛素化依赖性降解来负调控肿瘤抑制因子 TRIM16,最终激活与细胞周期和上皮-间充质转化(EMT)相关的途径。总之,这些结果表明 RASSF6-TRIM16 轴是 ESCC 进展的关键效应因子,并且 RASSF6 可作为 ESCC 治疗的潜在靶点。