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里博西利联合吉西他滨治疗髓母细胞瘤。

Combination of Ribociclib and Gemcitabine for the Treatment of Medulloblastoma.

机构信息

Department of Tumor Cell Biology, St. Jude Children's Research Hospital, Memphis, Tennessee.

Department of Computational Biology, St. Jude Children's Research Hospital, Memphis, Tennessee.

出版信息

Mol Cancer Ther. 2022 Aug 2;21(8):1306-1317. doi: 10.1158/1535-7163.MCT-21-0598.

Abstract

Group3 (G3) medulloblastoma (MB) is one of the deadliest forms of the disease for which novel treatment is desperately needed. Here we evaluate ribociclib, a highly selective CDK4/6 inhibitor, with gemcitabine in mouse and human G3MBs. Ribociclib central nervous system (CNS) penetration was assessed by in vivo microdialysis and by IHC and gene expression studies and found to be CNS-penetrant. Tumors from mice treated with short term oral ribociclib displayed inhibited RB phosphorylation, downregulated E2F target genes, and decreased proliferation. Survival studies to determine the efficacy of ribociclib and gemcitabine combination were performed on mice intracranially implanted with luciferase-labeled mouse and human G3MBs. Treatment of mice with the combination of ribociclib and gemcitabine was well tolerated, slowed tumor progression and metastatic spread, and increased survival. Expression-based gene activity and cell state analysis investigated the effects of the combination after short- and long-term treatments. Molecular analysis of treated versus untreated tumors showed a significant decrease in the activity and expression of genes involved in cell-cycle progression and DNA damage response, and an increase in the activity and expression of genes implicated in neuronal identity and neuronal differentiation. Our findings in both mouse and human patient-derived orthotopic xenograft models suggest that ribociclib and gemcitabine combination therapy warrants further investigation as a treatment strategy for children with G3MB.

摘要

Group3(G3)髓母细胞瘤(MB)是该疾病中最致命的形式之一,迫切需要新的治疗方法。在这里,我们评估了瑞博西利(一种高度选择性的 CDK4/6 抑制剂)与吉西他滨在小鼠和人 G3MB 中的联合应用。通过体内微透析和免疫组化及基因表达研究评估了瑞博西利的中枢神经系统(CNS)穿透性,并发现其具有 CNS 穿透性。用短期口服瑞博西利治疗的小鼠肿瘤显示 RB 磷酸化受到抑制,E2F 靶基因下调,增殖减少。对颅内植入荧光素酶标记的小鼠和人 G3MB 的小鼠进行了瑞博西利和吉西他滨联合治疗的生存研究,以确定其疗效。瑞博西利和吉西他滨联合治疗的小鼠耐受性良好,肿瘤进展和转移扩散速度减慢,生存时间延长。对短期和长期治疗后的联合治疗进行基于表达的基因活性和细胞状态分析。对治疗和未治疗的肿瘤进行分子分析表明,参与细胞周期进程和 DNA 损伤反应的基因的活性和表达显著降低,而与神经元身份和神经元分化相关的基因的活性和表达增加。我们在小鼠和人源性原位异种移植模型中的发现表明,瑞博西利和吉西他滨联合治疗作为 G3MB 儿童的治疗策略值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/882b/9662921/e70561484f65/1306fig1.jpg

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