ZEB1是髓母细胞瘤预后的亚群特异性标志物和潜在的药物靶点。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2023-03-01 DOI:10.1007/s12017-022-08716-z
Livia Fratini, Matheus Gibeke Siqueira Dalmolin, Marialva Sinigaglia, Alexandre da Silveira Perla, Caroline Brunetto de Farias, Algemir L Brunetto, André T Brunetto, Mariane da Cunha Jaeger, Rafael Roesler
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引用次数: 1

摘要

髓母细胞瘤(Medulloblastoma, MB)是一种恶性脑肿瘤,主要发生于儿童和青少年,并表现为四个不同的分子亚群,分别为WNT, SHH, Group 3和Group 4。ZEB1是一种促进间充质标志物表达,抑制上皮和极性基因表达的转录因子。由于ZEB1参与小脑发育,我们研究了ZEB1在MB中的作用。我们发现,与正常小脑组织相比,MB肿瘤样本中ZEB1的表达增加。与所有其他MB分子亚组相比,SHH亚组的表达更高。在3组和4组中,ZEB1高表达与预后差相关,而在WNT肿瘤患者中,ZEB1低表达与预后差相关。在第3组和第4组MB中,ZEB1和MYC的表达有中度相关性。用免疫调节剂和组蛋白去乙酰化酶(HDAC)抑制剂fingolimod (FTY720)治疗可以降低D283细胞中ZEB1的表达。这些发现揭示了ZEB1表达与MB患者生存之间新的亚组特异性关联,并表明靶向HDAC活性的药物可以降低ZEB1表达。
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ZEB1 is a Subgroup-Specific Marker of Prognosis and Potential Drug Target in Medulloblastoma.

Medulloblastoma (MB) is a malignant brain tumor that afflicts mostly children and adolescents and presents four distinct molecular subgroups, known as WNT, SHH, Group 3, and Group 4. ZEB1 is a transcription factor that promotes the expression of mesenchymal markers while restraining expression of epithelial and polarity genes. Because of ZEB1 involvement in cerebellum development, here we investigated the role of ZEB1 in MB. We found increased expression of ZEB1 in MB tumor samples compared to normal cerebellar tissue. Expression was higher in the SHH subgroup when compared to all other MB molecular subgroups. High ZEB1 expression was associated with poor prognosis in Group 3 and Group 4, whereas in patients with WNT tumors poorer prognosis were related to lower ZEB1 expression. There was a moderate correlation between ZEB1 and MYC expression in Group 3 and Group 4 MB. Treatment with the immunomodulator and histone deacetylase (HDAC) inhibitor fingolimod (FTY720) reduced ZEB1 expression specifically in D283 cells, which are representative of Group 3 and Group 4 MB. These findings reveal novel subgroup-specific associations of ZEB1 expression with survival in patients with MB and suggest that ZEB1 expression can be reduced by pharmacological agents that target HDAC activity.

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7.20
自引率
4.30%
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567
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