Pediatric brain tumors as a developmental disease

被引:5
作者
Bruschi, Marco [1 ,2 ]
Grill, Jacques [1 ,2 ,3 ]
Guerrini-Rousseau, Lea [1 ,2 ,3 ]
机构
[1] Gustave Roussy, INSERM, Team Genom & Oncogenesis Pediat Brain Tumors, Unit Biomarkers & New Therapeut Canc 981, Villejuif, France
[2] Univ Paris Saclay, Villejuif, France
[3] Gustave Roussy, Dept Pediat & Adolescent Oncol, Villejuif, France
关键词
brain malformation; cancer predisposition; child; glioma; medulloblastoma; STEM-CELLS; CEREBRAL ORGANOIDS; GLIOMAS; MUTATIONS;
D O I
10.1097/CCO.0000000000000782
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of review Brain tumors are the most frequent solid cancer in the pediatric population. Owing to the rarity of environmental clues about their origin, it is tempting to consider these neoplasms as developmental processes gone awry. Our review will explore the heuristic power of this hypothesis and the influence of these findings on the clinical management. Recent finding A more accurate description of cancer predisposition syndrome has shown their frequent association with developmental abnormalities. Several genes involved in pediatric brain tumor oncogenesis are involved in developmental processes. Modeling of several pediatric brain tumor in cerebral organoids, mimicking embryonal stage of brain development, indicates that early events during brain development create the conditions necessary for their oncogenesis. The onset of multiple brain tumor types early in life suggests a functional relationship between brain development and oncogenesis. A growing body of evidence seems to support the hypothesis that some of the main developmental steps in the brain can be highjacked by the tumors during their initiation. Collaborations between neuroscientists and oncologists should provide room for improvement in the knowledge for these neoplasms.
引用
收藏
页码:608 / 614
页数:7
相关论文
共 48 条
[1]   Pediatric Gliomas as Neurodevelopmental Disorders [J].
Baker, Suzanne J. ;
Ellison, David W. ;
Gutmann, David H. .
GLIA, 2016, 64 (06) :879-895
[2]   Modeling medulloblastoma in vivo and with human cerebellar organoids [J].
Ballabio, Claudio ;
Anderle, Marica ;
Gianesello, Matteo ;
Lago, Chiara ;
Miele, Evelina ;
Cardano, Marina ;
Aiello, Giuseppe ;
Piazza, Silvano ;
Caron, Davide ;
Gianno, Francesca ;
Ciolfi, Andrea ;
Pedace, Lucia ;
Mastronuzzi, Angela ;
Tartaglia, Marco ;
Locatelli, Franco ;
Ferretti, Elisabetta ;
Giangaspero, Felice ;
Tiberi, Luca .
NATURE COMMUNICATIONS, 2020, 11 (01)
[3]   An early cell shape transition drives evolutionary expansion of the human forebrain [J].
Benito-Kwiecinski, Silvia ;
Giandomenico, Stefano L. ;
Sutcliffe, Magdalena ;
Riis, Erlend S. ;
Freire-Pritchett, Paula ;
Kelava, Iva ;
Wunderlich, Stephanie ;
Martin, Ulrich ;
Wray, Gregory A. ;
McDole, Kate ;
Lancaster, Madeline A. .
CELL, 2021, 184 (08) :2084-+
[4]   Genetically engineered cerebral organoids model brain tumor formation [J].
Bian, Shan ;
Repic, Marko ;
Guo, Zhenming ;
Kavirayani, Anoop ;
Burkard, Thomas ;
Bagley, Joshua A. ;
Krauditsch, Christian ;
Knoblich, Juergen A. .
NATURE METHODS, 2018, 15 (08) :631-+
[5]   Consensus Statement From the First International Colloquium on Basal Cell Nevus Syndrome (BCNS) [J].
Bree, Alanna F. ;
Shah, Maulik R. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2011, 155A (09) :2091-2097
[6]   Humanized Stem Cell Models of Pediatric Medulloblastoma Reveal an Oct4/mTOR Axis that Promotes Malignancy [J].
Cancer, Matko ;
Hutter, Sonja ;
Holmberg, Karl O. ;
Rosen, Gabriela ;
Sundstrom, Anders ;
Tailor, Jignesh ;
Bergstrom, Tobias ;
Garancher, Alexandra ;
Essand, Magnus ;
Wechsler-Reya, Robert J. ;
Falk, Anna ;
Weishaupt, Holger ;
Swartling, Fredrik J. .
CELL STEM CELL, 2019, 25 (06) :855-+
[7]   DNA methylation-based classification of central nervous system tumours [J].
Capper, David ;
Jones, David T. W. ;
Sill, Martin ;
Hovestadt, Volker ;
Schrimpf, Daniel ;
Sturm, Dominik ;
Koelsche, Christian ;
Sahm, Felix ;
Chavez, Lukas ;
Reuss, David E. ;
Kratz, Annekathrin ;
Wefers, Annika K. ;
Huang, Kristin ;
Pajtler, Kristian W. ;
Schweizer, Leonille ;
Stichel, Damian ;
Olar, Adriana ;
Engel, Nils W. ;
Lindenberg, Kerstin ;
Harter, Patrick N. ;
Braczynski, Anne K. ;
Plate, Karl H. ;
Dohmen, Hildegard ;
Garvalov, Boyan K. ;
Coras, Roland ;
Hoelsken, Annett ;
Hewer, Ekkehard ;
Bewerunge-Hudler, Melanie ;
Schick, Matthias ;
Fischer, Roger ;
Beschorner, Rudi ;
Schittenhelm, Jens ;
Staszewski, Ori ;
Wani, Khalida ;
Varlet, Pascale ;
Pages, Melanie ;
Temming, Petra ;
Lohmann, Dietmar ;
Selt, Florian ;
Witt, Hendrik ;
Milde, Till ;
Witt, Olaf ;
Aronica, Eleonora ;
Giangaspero, Felice ;
Rushing, Elisabeth ;
Scheurlen, Wolfram ;
Geisenberger, Christoph ;
Rodriguez, Fausto J. ;
Becker, Albert ;
Preusser, Matthias .
NATURE, 2018, 555 (7697) :469-+
[8]   Histone H3 wild-type DIPG/DMG overexpressing EZHIP extend the spectrum diffuse midline gliomas with PRC2 inhibition beyond H3-K27M mutation [J].
Castel, David ;
Kergrohen, Thomas ;
Tauziede-Espariat, Arnault ;
Mackay, Alan ;
Ghermaoui, Samia ;
Lechapt, Emmanuele ;
Pfister, Stefan M. ;
Kramm, Christof M. ;
Boddaert, Nathalie ;
Blauwblomme, Thomas ;
Puget, Stephanie ;
Beccaria, Kevin ;
Jones, Chris ;
Jones, David T. W. ;
Varlet, Pascale ;
Grill, Jacques ;
Debily, Marie-Anne .
ACTA NEUROPATHOLOGICA, 2020, 139 (06) :1109-1113
[9]   Histone H3F3A and HIST1H3B K27M mutations define two subgroups of diffuse intrinsic pontine gliomas with different prognosis and phenotypes [J].
Castel, David ;
Philippe, Cathy ;
Calmon, Raphael ;
Le Dret, Ludivine ;
Truffaux, Nathalene ;
Boddaert, Nathalie ;
Pages, Melanie ;
Taylor, Kathryn R. ;
Saulnier, Patrick ;
Lacroix, Ludovic ;
Mackay, Alan ;
Jones, Chris ;
Sainte-Rose, Christian ;
Blauwblomme, Thomas ;
Andreiuolo, Felipe ;
Puget, Stephanie ;
Grill, Jacques ;
Varlet, Pascale ;
Debily, Marie-Anne .
ACTA NEUROPATHOLOGICA, 2015, 130 (06) :815-827
[10]   An update on the central nervous system manifestations of DICER1 syndrome [J].
de Kock, Leanne ;
Priest, John R. ;
Foulkes, William D. ;
Alexandrescu, Sanda .
ACTA NEUROPATHOLOGICA, 2020, 139 (04) :689-701