Targeting the Hedgehog Pathway in Pediatric Medulloblastoma

被引:41
作者
Huang, Sherri Y. [1 ]
Yang, Jer-Yen [2 ,3 ]
机构
[1] Indiana Univ, Sch Med, Dept Pharmacol & Toxicol, Indianapolis, IN 46202 USA
[2] Purdue Univ, Dept Basic Med Sci, Coll Vet Med, W Lafayette, IN 47906 USA
[3] Purdue Univ, Ctr Canc Res, W Lafayette, IN 47906 USA
基金
芬兰科学院;
关键词
hedgehog; Gli1; medulloblastoma; BASAL-CELL CARCINOMAS; TRANSCRIPTIONAL ACTIVITY; CEREBELLAR DEVELOPMENT; NUCLEAR-LOCALIZATION; SIGNALING PATHWAY; CYCLIC-AMP; STEM-CELLS; PHASE-II; GLI1; INHIBITION;
D O I
10.3390/cancers7040880
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Medulloblastoma (MB), a primitive neuroectomal tumor of the cerebellum, is the most common malignant pediatric brain tumor. The cause of MB is largely unknown, but aberrant activation of Hedgehog (Hh) pathway is responsible for similar to 30% of MB. Despite aggressive treatment with surgical resection, radiation and chemotherapy, 70%-80% of pediatric medulloblastoma cases can be controlled, but most treated patients suffer devastating side effects. Therefore, developing a new effective treatment strategy is urgently needed. Hh signaling controls transcription of target genes by regulating activities of the three Glioma-associated oncogene (Gli1-3) transcription factors. In this review, we will focus on current clinical treatment options of MB and discuss mechanisms of drug resistance. In addition, we will describe current known molecular pathways which crosstalk with the Hedgehog pathway both in the context of medulloblastoma and non-medulloblastoma cancer development. Finally, we will introduce post-translational modifications that modulate Gli1 activity and summarize the positive and negative regulations of the Hh/Gli1 pathway. Towards developing novel combination therapies for medulloblastoma treatment, current information on interacting pathways and direct regulation of Hh signaling should prove critical.
引用
收藏
页码:2110 / 2123
页数:14
相关论文
共 97 条
[1]   Unraveling the therapeutic potential of the Hedgehog pathway in cancer [J].
Amakye, Dereck ;
Jagani, Zainab ;
Dorsch, Marion .
NATURE MEDICINE, 2013, 19 (11) :1410-1422
[2]   Isolated Sensorineural Hearing Loss as Initial Presentation of Recurrent Medulloblastoma: Neuroimaging and Audiologic Correlates [J].
Amene, C. S. ;
Yeh-Nayre, L. A. ;
Crawford, J. R. .
CLINICAL NEURORADIOLOGY, 2013, 23 (04) :301-303
[3]   Canonical TGF-β Pathway Activity Is a Predictor of SHH-Driven Medulloblastoma Survival and Delineates Putative Precursors in Cerebellar Development [J].
Aref, Donya ;
Moffatt, Connor J. ;
Agnihotri, Sameer ;
Ramaswamy, Vijay ;
Dubuc, Adrian M. ;
Northcott, Paul A. ;
Taylor, Michael D. ;
Perry, Arie ;
Olson, James M. ;
Eberhart, Charles G. ;
Croul, Sidney E. .
BRAIN PATHOLOGY, 2013, 23 (02) :178-191
[4]   Identification of a Suppressive Mechanism for Hedgehog Signaling through a Novel Interaction of Gli with 14-3-3 [J].
Asaoka, Yoshinari ;
Kanai, Fumihiko ;
Ichimura, Tohru ;
Tateishi, Keisuke ;
Tanaka, Yasuo ;
Ohta, Miki ;
Seto, Motoko ;
Tada, Motohisa ;
Ijichi, Hideaki ;
Ikenoue, Tsuneo ;
Kawabe, Takao ;
Isobe, Toshiaki ;
Yaffe, Michael B. ;
Omata, Masao .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (06) :4185-4194
[5]   Inhibition of Smoothened signaling prevents ultraviolet B-induced basal cell carcinomas through regulation of Fas expression and apoptosis [J].
Athar, M ;
Li, CX ;
Tang, XW ;
Chi, SM ;
Zhang, XL ;
Kim, AL ;
Tyring, SK ;
Kopelovich, L ;
Hebert, J ;
Epstein, EH ;
Bickers, DR ;
Xie, JW .
CANCER RESEARCH, 2004, 64 (20) :7545-7552
[6]   Sonic hedgehog induces transcription-independent cytoskeletal rearrangement and migration regulated by arachidonate metabolites [J].
Bijlsma, Maarten F. ;
Borensztajn, Keren S. ;
Roelink, Henk ;
Peppelenbosch, Maikel P. ;
Spek, C. Arnold .
CELLULAR SIGNALLING, 2007, 19 (12) :2596-2604
[7]   Survivin as a therapeutic target in Sonic hedgehog-driven medulloblastoma [J].
Brun, S. N. ;
Markant, S. L. ;
Esparza, L. A. ;
Garcia, G. ;
Terry, D. ;
Huang, J-M ;
Pavlyukov, M. S. ;
Li, X-N ;
Grant, G. A. ;
Crawford, J. R. ;
Levy, M. L. ;
Conway, E. M. ;
Smith, L. H. ;
Nakano, I. ;
Berezov, A. ;
Greene, M. I. ;
Wang, Q. ;
Wechsler-Reya, R. J. .
ONCOGENE, 2015, 34 (29) :3770-3779
[8]   Interfering with Resistance to Smoothened Antagonists by Inhibition of the PI3K Pathway in Medulloblastoma [J].
Buonamici, Silvia ;
Williams, Juliet ;
Morrissey, Michael ;
Wang, Anlai ;
Guo, Ribo ;
Vattay, Anthony ;
Hsiao, Kathy ;
Yuan, Jing ;
Green, John ;
Ospina, Beatriz ;
Yu, Qunyan ;
Ostrom, Lance ;
Fordjour, Paul ;
Anderson, Dustin L. ;
Monahan, John E. ;
Kelleher, Joseph F. ;
Peukert, Stefan ;
Pan, Shifeng ;
Wu, Xu ;
Maira, Sauveur-Michel ;
Garcia-Echeverria, Carlos ;
Briggs, Kimberly J. ;
Watkins, D. Neil ;
Yao, Yung-mae ;
Lengauer, Christoph ;
Warmuth, Markus ;
Sellers, William R. ;
Dorsch, Marion .
SCIENCE TRANSLATIONAL MEDICINE, 2010, 2 (51)
[9]   Protein Kinase Cδ Negatively Regulates Hedgehog Signaling by Inhibition of Gli1 Activity [J].
Cai, Qingsong ;
Li, Jing ;
Gao, Tianyan ;
Xie, Jingwu ;
Evers, B. Mark .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (04) :2150-2158
[10]   Activity-dependent internalization of smoothened mediated by β-arrestin 2 and GRK2 [J].
Chen, W ;
Ren, XR ;
Nelson, CD ;
Barak, LS ;
Chen, JK ;
Beachy, PA ;
de Sauvage, F ;
Lefkowitz, RJ .
SCIENCE, 2004, 306 (5705) :2257-2260