Comprehensive genomics linking between neural development and cancer: neuroblastoma as a model.

Abstract:

:Cancer cells are derived from their precursor cells, which normally develop to the matured cells to form individual organs. Neuroblastoma, one of the most common pediatric solid tumors, originates from possible cancer stem cells derived from the neural crest. During the development, neural crest cells segregate into several lineages such as sensory, enteric and sympathetic neurons. However, the genetic events to cause neuroblastoma occur only in the sympathetic precursor cells or cancer stem cells. Furthermore, spontaneous regression of a subset of neuroblastoma found in patients under one year of age mimics a developmentally programmed neuronal cell death that occurs in normal sympathetic neurons during the perinatal period. Thus, the genetic events to cause neuroblastoma may be programmed to occur in a lineage-specific as well as developmentally regulated manner. In this review, we discuss about the molecular link between neural development and the genesis of neuroblastoma based on our comprehensive genomics approach.

journal_name

Cancer Lett

journal_title

Cancer letters

authors

Nakagawara A,Ohira M

doi

10.1016/S0304-3835(03)00457-9

keywords:

subject

Has Abstract

pub_date

2004-02-20 00:00:00

pages

213-24

issue

2

eissn

0304-3835

issn

1872-7980

pii

S0304383503004579

journal_volume

204

pub_type

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