Abstract:
:In retinoblastoma, genetic alteration of N-myc amplification different from the alteration of the RB1 gene on chromosome 13q14 has been described. This study is to determine the frequency of N-myc amplification by fluorescence in situ hybridization method in retinoblastoma. This study was prospectively derived from 26 patients who were diagnosed as having unilateral retinoblastoma (highly progressive large retinoblastoma, group 5 in Reese-Ellsworth classification) and underwent enucleation. We performed locus-specific fluorescence in situ hybridization probes for N-myc gene. Our results demonstrated that in only one of 26 patients was N-myc amplification found in retinoblastoma tissue. N-myc amplification has been regarded as one characteristic of retinoblastoma cell line and an adverse prognostic factor. However, our study indicates that N-myc amplification is not frequently found in retinoblastoma.
journal_name
Hum Patholjournal_title
Human pathologyauthors
Kim JH,Choi JM,Yu YS,Kim DH,Kim JH,Kim KWdoi
10.1016/j.humpath.2007.12.008subject
Has Abstractpub_date
2008-08-01 00:00:00pages
1172-5issue
8eissn
0046-8177issn
1532-8392pii
S0046-8177(07)00712-5journal_volume
39pub_type
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