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YAP1是髓母细胞瘤细胞中对SMO抑制剂反应的潜在预测性分子生物标志物。

YAP1 Is a Potential Predictive Molecular Biomarker for Response to SMO Inhibitor in Medulloblastoma Cells.

作者信息

Alencastro Veiga Cruzeiro Gustavo, de Almeida Magalhães Taciani, Ribeiro de Sousa Graziella, Bonfim Silva Ricardo, Alberto Oliveira de Biagi Junior Carlos, Ferreira das Chagas Pablo, Gomes de Paula Queiroz Rosane, Alberto Scrideli Carlos, Gonzaga Tone Luiz, Terci Valera Elvis

机构信息

Department of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, Hospital das Clínicas Ribeirão Preto, Av. Bandeirantes 3900, Ribeirão Preto 05468901, São Paulo, Brazil.

Department of Pediatric Oncology, Dana-Farber Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, 450 Brookline Avenue, Boston, MA 02215, USA.

出版信息

Cancers (Basel). 2021 Dec 13;13(24):6249. doi: 10.3390/cancers13246249.

Abstract

Advances in genomics have led to the identification of twelve relevant molecular subtypes within medulloblastoma (MB). The alpha subtype of Sonic hedgehog-driven MB is resistant to therapy (including smoothened inhibitors) due to activation of genes from the non-canonical SHH pathway, such as , , or . Using retrospective cohort microarray data, we found that is overexpressed in SHH alpha MB and patients profiled as resistant to SMO inhibitors compared to good responders. Here, we performed depletion via CRISPR/Cas9 in two in vitro models of SHH-like MB cells and found that this protein is involved in responsiveness to the SMO inhibitor regarding proliferation, apoptosis, and colony formation. Further, considering the synergic combination of YAP1 depletion with SMO inhibition, we assessed single-cell RNA-seq data from five patients and found that and are enriched within cells of SHH MB. Importantly, our data suggest that is not only a reliable biomarker for cellular response to SMOi but may indicate prospective testing of combination therapy using YAP1 and SMO inhibitors in preclinical models of SHH MB.

摘要

基因组学的进展已导致在髓母细胞瘤(MB)中鉴定出12种相关分子亚型。由音猬因子(Sonic hedgehog)驱动的MB的α亚型由于非经典SHH途径的基因激活,如 、 或 ,而对治疗(包括 smoothened 抑制剂)耐药。利用回顾性队列微阵列数据,我们发现与反应良好者相比, 在SHHα MB和被描述为对SMO抑制剂耐药的患者中过表达。在此,我们在两种SHH样MB细胞的体外模型中通过CRISPR/Cas9进行了 缺失实验,发现该蛋白在增殖、凋亡和集落形成方面参与了对SMO抑制剂的反应。此外,考虑到YAP1缺失与SMO抑制的协同组合,我们评估了5名患者的单细胞RNA测序数据,发现 和 在SHH MB细胞中富集。重要的是,我们的数据表明, 不仅是细胞对SMOi反应的可靠生物标志物,而且可能表明在SHH MB的临床前模型中使用YAP1和SMO抑制剂进行联合治疗的前瞻性测试。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/177b/8699675/d53426e8ed1f/cancers-13-06249-g001.jpg

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