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1.
Oncol Res ; 32(4): 607-614, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38560568

RESUMEN

C-mannosylation is a post-translational modification that occurs intracellularly in the endoplasmic reticulum. In humans, biosynthesis of C-mannosylation in proteins containing thrombospondin type 1 repeat is catalyzed by the DPY19 family; nonetheless, biological functions of protein C-mannosylation are not yet fully understood, especially in tumor progression. Vasculogenic mimicry (VM) is the formation of fluid-conducting channels by highly invasive and genetically deregulated tumor cells, enabling the tumors to form matrix-embedded vasculogenic structures, containing plasma and blood cells to meet the metabolic demands of rapidly growing tumors. In this study, we focused on DPY19L3, a C-mannosyltransferase, and aimed to unravel its role in VM. Knockout of DPY19L3 inhibited the formation of VM in HT1080 human fibrosarcoma cells. Re-expression of wild-type DPY19L3 recovered VM formation; however, DPY19L3 isoform2, an enzymatic activity-defect mutant, did not restore it, suggesting that the C-mannosyltransferase activity of DPY19L3 is crucial to its function. Furthermore, the knockdown of DPY19L3 in MDA-MB-231 breast cancer cells hindered its network formation ability. Altogether, our findings suggest that DPY19L3 is required for VM formation and stipulate the relevance of C-mannosylation in oncogenesis.


Asunto(s)
Neoplasias de la Mama , Manosiltransferasas , Femenino , Humanos , Neoplasias de la Mama/patología , Línea Celular Tumoral , Manosiltransferasas/genética , Manosiltransferasas/metabolismo , Neovascularización Patológica/genética , Neovascularización Patológica/metabolismo
2.
Molecules ; 26(18)2021 Sep 19.
Artículo en Inglés | MEDLINE | ID: mdl-34577156

RESUMEN

DPY19L3 has been identified as a C-mannosyltransferase for thrombospondin type-1 repeat domain-containing proteins. In this study, we focused on the role of DPY19L3 in the myogenic differentiation of C2C12 mouse myoblast cells. We carried out DPY19L3 gene depletion using the CRISPR/Cas9 system. The result showed that these DPY19L3-knockout cells could not be induced for differentiation. Moreover, the phosphorylation levels of MEK/ERK and p70S6K were suppressed in the DPY19L3-knockout cells compared with that of parent cells, suggesting that the protein(s) that is(are) DPY19L3-mediated C-mannosylated and regulate(s) MEK/ERK or p70S6K signaling is(are) required for the differentiation.


Asunto(s)
Diferenciación Celular/genética , Diferenciación Celular/fisiología , Manosiltransferasas/fisiología , Mioblastos/fisiología , Animales , Línea Celular , Quinasas MAP Reguladas por Señal Extracelular/metabolismo , Técnicas de Silenciamiento del Gen , Glicosilación , Manosiltransferasas/genética , Ratones , Quinasas de Proteína Quinasa Activadas por Mitógenos/metabolismo , Mioblastos/citología , Fosforilación/genética , Proteínas Quinasas S6 Ribosómicas 70-kDa/metabolismo , Transducción de Señal/genética , Regulación hacia Arriba/genética
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