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

Cell death & disease (2024-01-14)
Sara Basbous, Lydia Dif, Camille Dantzer, Sylvaine Di-Tommaso, Jean-William Dupuy, Paulette Bioulac-Sage, Anne-Aurélie Raymond, Chantal Desdouets, Frédéric Saltel, Violaine Moreau
RÉSUMÉ

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.

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Sigma-Aldrich
Anti--actine antibody produced in rabbit, affinity isolated antibody, buffered aqueous solution
Sigma-Aldrich
Anticorps anti-phospho-MYPT1 (Thr696), from rabbit, purified by affinity chromatography
Sigma-Aldrich
Anti-MYPT1 Antibody, from rabbit, purified by affinity chromatography