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Detection of N‐ myc amplification by FISH in immature areas of fixed neuroblastomas: more efficient than Southern blot/PCR
Author(s) -
Sartelet Hervé,
Grossi Laurence,
Pasquier Dominique,
Combaret Valérie,
Bouvier Raymonde,
Ranchère Dominique,
Plantaz Dominique,
Munzer Martine,
Philip Thierry,
Birembaut Philippe,
Zahm JeanMarie,
Bergeron Christophe,
Gaillard Dominique,
Pasquier Basile
Publication year - 2002
Publication title -
the journal of pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.964
H-Index - 184
eISSN - 1096-9896
pISSN - 0022-3417
DOI - 10.1002/path.1182
Subject(s) - southern blot , biology , polymerase chain reaction , fluorescence in situ hybridization , microbiology and biotechnology , dot blot , fish <actinopterygii> , n myc , western blot , gene duplication , blot , neuroblastoma , gene , genetics , ganglioneuroma , cell culture , fishery , chromosome
N‐ myc amplification is a major prognostic factor in neuroblastomas and is systematically investigated by Southern blot or polymerase chain reaction (PCR). A retrospective study of N ‐myc amplification has been carried out using fluorescence in situ hybridization (FISH) in 97 fixed neuroblastomas. For each tumour, FISH was performed on the area that contained the most immature neuroblasts. Among these 97 neuroblastomas, 16 were amplified and 12 were not interpretable. FISH was not interpretable in six cases. All neuroblastomas with N‐ myc amplification detected by Southern blot/PCR were amplified with FISH, except three that were not interpretable. Four tumours that were not interpretable in Southern blot/PCR contained more than five copies of N‐ myc by FISH: one was aneuploid and three were truly amplified, containing more than ten copies of N‐ myc . Among these three patients, two died in a short time of their tumours. Ten cases were not amplified by Southern blot/PCR and showed more than five copies by FISH: four were aneuploid and two showed heterogeneous amplification, with a few cells clearly amplified whereas most were not. Four cases were amplified, of which two patients died of their tumours. This study confirms that when applied to the most immature areas of fixed neuroblastomas, FISH displayed a higher sensitivity than molecular techniques ( p < 0.001) and could detect heterogeneous amplification. FISH could therefore become an important complementary procedure in assessing prognosis in neuroblastomas. Copyright © 2002 John Wiley & Sons, Ltd.