The developmental stage of the medulloblastoma cell-of-origin restricts Sonic hedgehog pathway usage and drug sensitivity

被引:5
作者
Smit, Marlinde J. [1 ]
Martini, Tosca E., I [1 ]
Armandari, Inna [1 ]
Bockaj, Irena [1 ]
Zomerman, Walderik W. [2 ]
de Camargo Magalhaes, Eduardo S. [1 ,3 ]
Siragna, Zillah [1 ]
Meeuwsen, Tiny G. J. [4 ]
Scherpen, Frank J. G. [4 ]
Schoots, Mirthe H. [4 ]
Ritsema, Martha [1 ]
den Dunnen, Wilfred F. A. [4 ]
Hoving, Eelco W. [5 ]
Paridaen, Judith T. M. L. [1 ]
de Haan, Gerald [1 ,6 ]
Guryev, Victor [1 ]
Bruggeman, Sophia W. M. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, European Res Inst Biol Ageing ERIBA, Hanzepl 1, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Pediat Pediat Oncol & Hematol, Hanzepl 1, NL-9700 RB Groningen, Netherlands
[3] Univ Fed Rio de Janeiro, Biomed Sci Inst, Glial Cell Biol Lab, BR-21949590 Rio De Janeiro, Brazil
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol & Med Biol, Hanzepl 1, NL-9700 RB Groningen, Netherlands
[5] Princess Maxima Ctr Pediat Oncol, Lundlaan 6, NL-3584 EA Utrecht, Netherlands
[6] Univ Amsterdam, Amsterdam UMC, Sanquin Res & Landsteiner Lab, Dept Hernalopoiesis, NL-1066 CX Amsterdam, Netherlands
关键词
Medulloblastoma; Sonic hedgehog signaling; Cerebellar development; Cerebellar granule neuron progenitors; Tumor cell-of-origin; Primary cilia; PRIMARY CILIA; CEREBELLAR MORPHOGENESIS; SHH MEDULLOBLASTOMA; REPRESSOR FUNCTIONS; EXPRESSION; PROLIFERATION; SUPPRESSOR; STEM; EXPANSION; MATH1;
D O I
10.1242/jcs.258608
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sonic hedgehog (SHH) medulloblastoma originates from the cerebellar granule neuron progenitor (CGNP) lineage, which depends on Hedgehog signaling for its perinatal expansion. Whereas SHH tumors exhibit overall deregulation of this pathway, they also show patient age-specific aberrations. To investigate whether the developmental stage of the CGNP can account for these age-specific lesions, we analyzed developing murine CGNP transcriptomes and observed highly dynamic gene expression as a function of age. Cross-species comparison with human SHH medulloblastoma showed partial maintenance of these expression patterns, and highlighted low primary cilium expression as hallmark of infant medulloblastoma and early embryonic CGNPs. This coincided with reduced responsiveness to upstream SHH pathway component Smoothened, whereas sensitivity to downstream components SUFU and GLI family proteins was retained. Together, these findings can explain the preference for SUFU mutations in infant medulloblastoma and suggest that drugs targeting the downstream SHH pathway will be most appropriate for infant patients.
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页数:14
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