癌症研究
河马信号通路
活力测定
信号转导
免疫印迹
生物
微阵列分析技术
体内
组蛋白脱乙酰基酶
生物发光成像
化学
表观遗传学
细胞生长
基因沉默
神经球
细胞生物学
细胞
胶质母细胞瘤
生物途径
微阵列
基因表达
下调和上调
骨膜炎
基因表达调控
细胞培养
替莫唑胺
HMGA2型
作者
Tae Hoon Roh,Hye Eun Byeon,Seo Jin Kim,Seonah Choi,Ju Hyung Moon,Eui Hyun Kim,Seok-Gu Kang,Jong Hee Chang
出处
期刊:Neuro-oncology
[Oxford University Press]
日期:2025-11-01
卷期号:27 (Supplement_5): v86-v86
标识
DOI:10.1093/neuonc/noaf201.0347
摘要
Abstract Glioblastoma (GBM) is characterized by high morbidity and resistance to conventional therapies. Targeting epigenetic regulators and signaling pathways may offer novel therapeutic avenues. In this study, we evaluated the therapeutic impact of combining the HDAC inhibitor SAHA (suberoylanilide hydroxamic acid) with Verteporfin, a Hippo signaling pathway regulator, in patient-derived GBM tumor spheres (TS13-64 and TS15-88). We assessed cell viability, synergy scores, ATP activity, and protein expression through Western blot analysis. Gene expression changes were analyzed using microarray and RNA sequencing. Additionally, in vivo studies were conducted using bioluminescence imaging and survival analysis in luciferase-tagged TS13-64 orthotopic xenograft models. The combination of SAHA and Verteporfin significantly reduced cell viability and yielded high synergy scores, indicating an effective interaction between the two drugs. Microarray and real-time PCR analyses revealed decreased HDAC and YAP expression following treatment. We also observed reduced stemness and invasiveness of GBM tumor spheres, as evidenced by decreased neurosphere formation and altered protein expression profiles associated with these phenotypes. In vivo, the combined treatment led to a significant decrease in bioluminescence intensity, suggesting reduced tumor burden. Survival analysis showed a trend toward prolonged survival in treated animals. Our findings suggest that combined modulation of HDAC activity and Hippo pathway signaling represents a promising therapeutic strategy for GBM. This dual-targeted approach may overcome current treatment resistance and improve clinical outcomes in GBM patients.
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