Loss of RND3/RHOE controls entosis through LAMP1 expression in hepatocellular carcinoma

被引:5
作者
Basbous, Sara [1 ]
Dif, Lydia [1 ]
Dantzer, Camille [1 ]
Di-Tommaso, Sylvaine [2 ,3 ]
Dupuy, Jean-William [3 ,4 ]
Bioulac-Sage, Paulette [1 ,2 ]
Raymond, Anne-Aurelie [1 ,3 ]
Desdouets, Chantal [5 ]
Saltel, Frederic [1 ,3 ]
Moreau, Violaine [1 ]
机构
[1] Univ Bordeaux, INSERM, BRIC, U1312, Bordeaux, France
[2] CHU Bordeaux, F-33076 Bordeaux, France
[3] Univ Bordeaux, Oncoprot Platform, UMS005, TBMCore, F-33076 Bordeaux, France
[4] Univ Bordeaux, Prote Plateform, F-33076 Bordeaux, France
[5] Sorbonne Univ, Ctr Rech Cordeliers CRC, INSERM, Paris, France
关键词
CELL-DEATH; RHOE;
D O I
10.1038/s41419-024-06420-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Entosis is a process that leads to the formation of cell-in-cell structures commonly found in cancers. Here, we identified entosis in hepatocellular carcinoma and the loss of Rnd3 (also known as RhoE) as an efficient inducer of this mechanism. We characterized the different stages and the molecular regulators of entosis induced after Rnd3 silencing. We demonstrated that this process depends on the RhoA/ROCK pathway, but not on E-cadherin. The proteomic profiling of entotic cells allowed us to identify LAMP1 as a protein upregulated by Rnd3 silencing and implicated not only in the degradation final stage of entosis, but also in the full mechanism. Moreover, we found a positive correlation between the presence of entotic cells and the metastatic potential of tumors in human patient samples. Altogether, these data suggest the involvement of entosis in liver tumor progression and highlight a new perspective for entosis analysis in medicine research as a novel therapeutic target.
引用
收藏
页数:14
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