Guifa Xi,Barbara Mania-Farnell,Ting Lei,Tadanori Tomita. Histone modification as a drug resistance driver in brain tumors. Oncol Transl Med, 2016, 2: 216-226.
Histone modification as a drug resistance driver in brain tumors
Received:June 16, 2016  Revised:October 11, 2016
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KeyWord:histone modification; drug resistance; brain tumor
Author NameAffiliationE-mail
Guifa Xi Falk Brain Tumor Center, Division of Pediatric Neurosurgery, Ann & Robert H. Lurie Children’s Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL USA guifa.xi@northwestern.edu 
Barbara Mania-Farnell Purdue University Calumet, Hammond, IN USA bmania@pnw.edu 
Ting Lei Department of Neurosurgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China hufeng268@qq.com 
Tadanori Tomita Northwestern University Feinberg School of Medicine, Chicago, IL USA ttomita@luriechildrens.org 
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Abstract:
      Patients with brain tumors, specifically, malignant forms such as glioblastoma, medulloblastoma and ependymoma, exhibit dismal survival rates despite advances in treatment strategies. Chemotherapeutics, the primary adjuvant treatment for human brain tumors following surgery, commonly lack efficacy due to either intrinsic or acquired drug resistance. New treatments targeting epigenetic factors are being explored. Post-translational histone modification provides a critical regulatory platform for processes such as chromosome condensation and segregation, apoptosis, gene transcription, and DNA replication and repair. This work reviews how aberrant histone modifications and alterations in histone-modifying enzymes can drive the acquisition of drug resistance in brain tumors. Elucidating these mechanisms should lead to new treatments for overcoming drug resistance.
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