Chromogenic in situ hybridization using routine tissue sections : MYCN in neuroblastoma

Abstract

For detection of gene amplification, CISH has all the advantages of FISH but in addition, needs no special microscopy or image capturing systems, and preparations are permanent. In the case of neuroblastoma, CISH has disclosed considerable heterogeneity in MYCN copy number between cells in a tumour. Heterogeneity reflects different tumour clones and its role has been under-recognized in neuroblastoma biology. Additional studies are needed to investigate the significance of tumour heterogeneity in neuroblastoma, and whether the aggressive (i.e., MYCN-amplified) clones are more likely to metastasize, survive treatment modalities, and ultimately kill the patient.