Department of Neurosurgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Department of Ophthalmology, Jili Hospital of Liuyang (Liuyang Eye Hospital), Changsha, 410300, China.
Cell Death Dis. 2023 Mar 4;14(3):178. doi: 10.1038/s41419-023-05702-6.
Diffuse invasion is an important factor leading to treatment resistance and a poor prognosis in gliomas. Herein, we found that expression of the tripartite motif containing 56 (TRIM56), a RING-finger domain containing E3 ubiquitin ligase, was markedly higher in glioma than in normal brain tissue, and was significantly correlated with malignant phenotypes and a poor prognosis. In vitro and in vivo experimental studies revealed that TRIM56 promoted the migration and invasion of glioma cells. Mechanistically, TRIM56 was transcriptionally regulated by SP1 and promoted the K48-K63-linked poly-ubiquitination transition of IQGAP1 at Lys-1230 by interacting with it, which in turn promoted CDC42 activation. This mechanism was confirmed to mediate glioma migration and invasion. In conclusion, our study provides insights into the mechanisms through which TRIM56 promotes glioma motility, i.e., by regulating IQGAP1 ubiquitination to promote CDC42 activation, which might be clinically targeted for the treatment of glioma.
弥漫性浸润是导致胶质瘤治疗抵抗和预后不良的重要因素。在这里,我们发现三结构域蛋白 56(TRIM56)的表达在胶质瘤中明显高于正常脑组织,并且与恶性表型和不良预后显著相关。体外和体内实验研究表明,TRIM56 促进了胶质瘤细胞的迁移和侵袭。在机制上,TRIM56 受 SP1 转录调控,并通过与 IQGAP1 相互作用促进 IQGAP1 在 Lys-1230 处的 K48-K63 连接多泛素化转变,从而促进 CDC42 的激活。该机制被证实介导了胶质瘤的迁移和侵袭。总之,我们的研究提供了关于 TRIM56 促进胶质瘤运动的机制的见解,即通过调节 IQGAP1 的泛素化来促进 CDC42 的激活,这可能为治疗胶质瘤提供临床靶向。