Functionally defined therapeutic targets in diffuse intrinsic pontine glioma
弥漫性内生性脑桥胶质瘤的功能性治疗靶点
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作者:Catherine S Grasso,Yujie Tang,Nathalene Truffaux,Noah E Berlow,Lining Liu,Marie-Anne Debily,Michael J Quist,Lara E Davis,Elaine C Huang,Pamelyn J Woo,Anitha Ponnuswami,Spenser Chen,Tessa B Johung,Wenchao Sun,Mari Kogiso,Yuchen Du,Lin Qi,Yulun Huang,Marianne Hütt-Cabezas,Katherine E Warren,Ludivine Le Dret,Paul S Meltzer,Hua Mao,Martha Quezado,Dannis G van Vuurden,Jinu Abraham,Maryam Fouladi,Matthew N Svalina,Nicholas Wang,Cynthia Hawkins,Javad Nazarian,Marta M Alonso,Eric H Raabe,Esther Hulleman,Paul T Spellman,Xiao-Nan Li,Charles Keller,Ranadip Pal,Jacques Grill,Michelle Monje
| 期刊: | | 影响因子: | 58.700 |
| 时间: | 2015 | 起止号: | 2015 Jun;21(6):555-9. |
| doi: | PMC4862411 | 疾病类型: | 胶质瘤 |
Abstract
Diffuse intrinsic pontine glioma (DIPG) is a fatal childhood cancer. We performed a chemical screen in patient-derived DIPG cultures along with RNA-seq analyses and integrated computational modeling to identify potentially effective therapeutic strategies. The multi-histone deacetylase inhibitor panobinostat demonstrated therapeutic efficacy both in vitro and in DIPG orthotopic xenograft models. Combination testing of panobinostat and the histone demethylase inhibitor GSK-J4 revealed that the two had synergistic effects. Together, these data suggest a promising therapeutic strategy for DIPG.
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