TY - JOUR
T1 - PAX genes in childhood oncogenesis
T2 - Developmental biology gone awry?
AU - Mahajan, P.
AU - Leavey, P. J.
AU - Galindo, R. L.
N1 - Publisher Copyright:
© 2015 Macmillan Publishers Limited All rights reserved.
PY - 2015/5/21
Y1 - 2015/5/21
N2 - Childhood solid tumors often arise from embryonal-like cells, which are distinct from the epithelial cancers observed in adults, and etiologically can be considered as 'developmental patterning gone awry'. Paired-box (PAX) genes encode a family of evolutionarily conserved transcription factors that are important regulators of cell lineage specification, migration and tissue patterning. PAX loss-of-function mutations are well known to cause potent developmental phenotypes in animal models and underlie genetic disease in humans, whereas dysregulation and/or genetic modification of PAX genes have been shown to function as critical triggers for human tumorigenesis. Consequently, exploring PAX-related pathobiology generates insights into both normal developmental biology and key molecular mechanisms that underlie pediatric cancer, which are the topics of this review.
AB - Childhood solid tumors often arise from embryonal-like cells, which are distinct from the epithelial cancers observed in adults, and etiologically can be considered as 'developmental patterning gone awry'. Paired-box (PAX) genes encode a family of evolutionarily conserved transcription factors that are important regulators of cell lineage specification, migration and tissue patterning. PAX loss-of-function mutations are well known to cause potent developmental phenotypes in animal models and underlie genetic disease in humans, whereas dysregulation and/or genetic modification of PAX genes have been shown to function as critical triggers for human tumorigenesis. Consequently, exploring PAX-related pathobiology generates insights into both normal developmental biology and key molecular mechanisms that underlie pediatric cancer, which are the topics of this review.
UR - http://www.scopus.com/inward/record.url?scp=84930275898&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84930275898&partnerID=8YFLogxK
U2 - 10.1038/onc.2014.209
DO - 10.1038/onc.2014.209
M3 - Review article
C2 - 25043308
AN - SCOPUS:84930275898
SN - 0950-9232
VL - 34
SP - 2681
EP - 2689
JO - Oncogene
JF - Oncogene
IS - 21
ER -