PMID- 11821825 OWN - NLM STAT- MEDLINE DCOM- 20020306 LR - 20190916 IS - 0039-6060 (Print) IS - 0039-6060 (Linking) VI - 131 IP - 1 Suppl DP - 2002 Jan TI - Evaluation of genetic heterogeneity in neuroblastoma. PG - S283-7 AB - BACKGROUND AND METHODS: The prognosis in neuroblastoma, which is the most common solid tumor in children, tends to vary greatly, and many studies have demonstrated both clinical and biological factors to be closely correlated with the outcome. In order to select the optimal treatment according to the degree of malignancy of neuroblastoma, it is essential to accurately and rapidly identify any genetic heterogeneity associated with the prognosis. We assessed the status of some genetic abnormalities (MYCN amplification, deletion of the short arm of chromosome 1, DNA ploidy, and a gain of the chromosome 17q region) associated with the prognosis using several molecular biological methods. RESULTS AND CONCLUSIONS: The combination of several molecular biological techniques is thus considered to be useful for elucidating the degree of malignancy of neuroblastoma. In particular, diagnostic analyses based on a combination of the fluorescence in situ hybridization (FISH) method and the quantitative polymerase chain reaction (PCR) method may be considered to be the most effective methods for quickly and accurately evaluating any aberrations in the gene dosages associated with the patients' outcomes. FAU - Tajiri, Tatsuro AU - Tajiri T AD - Department of Pediatric Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan. FAU - Shono, Kumiko AU - Shono K FAU - Tanaka, Shinji AU - Tanaka S FAU - Suita, Sachiyo AU - Suita S LA - eng PT - Journal Article PL - United States TA - Surgery JT - Surgery JID - 0417347 SB - IM MH - *Chromosomes, Human, Pair 1 MH - *Chromosomes, Human, Pair 17 MH - Gene Deletion MH - Genetic Heterogeneity MH - Humans MH - In Situ Hybridization, Fluorescence MH - Neoplasms, Nerve Tissue/*genetics MH - Neuroblastoma/*genetics MH - Ploidies MH - Polymerase Chain Reaction EDAT- 2002/02/01 10:00 MHDA- 2002/03/07 10:01 CRDT- 2002/02/01 10:00 PHST- 2002/02/01 10:00 [pubmed] PHST- 2002/03/07 10:01 [medline] PHST- 2002/02/01 10:00 [entrez] AID - S0039-6060(02)08857-8 [pii] AID - 10.1067/msy.2002.119964 [doi] PST - ppublish SO - Surgery. 2002 Jan;131(1 Suppl):S283-7. doi: 10.1067/msy.2002.119964.