PMID- 24004585 OWN - NLM STAT- MEDLINE DCOM- 20140107 LR - 20181023 IS - 0529-5807 (Print) IS - 0529-5807 (Linking) VI - 42 IP - 5 DP - 2013 May TI - [Molecular genetic abnormalities of N-myc and C-myc in pediatric neuroblastic tumors and clinical pathologic significance]. PG - 299-304 LID - 10.3760/cma.j.issn.0529-5807.2013.05.003 [doi] AB - OBJECTIVE: To investigate the molecular genetic abnormalities of N-myc and C-myc, and their clinical pathological implications in pediatric neuroblastic tumors (NTs). METHODS: Abnormalities of N-myc were detected by interphase fluorescence in situ hybridization (FISH) technique in 246 cases of NTs, including neuroblastoma (NB,188 cases), ganglioneuroblastoma (GNB, 52 cases), ganglioneuroma (GN, 6 cases), and their association with the histological typing of the tumors and prognosis was analyzed. Abnormalities of C-myc were detected by FISH in 133 cases of NTs. RESULTS: Of the 246 cases of NTs, N-myc amplification was only found in 27 cases (11.0%, 27/246) of NB, but not in any cases of GNB or GN (P < 0.05). 89.0% (219/246) N-myc non-amplification were found in NTs, and it included N-myc gain in 175 cases (71.1%, 175/246) and normal N-myc in 44 cases (17.9%, 44/246). Univariate analysis indicated significantly (P = 0.012) poorer outcome in patients with N-myc amplification than N-myc non-amplification. However no significant difference was observed between N-myc gain cases and normal N-myc cases (P = 0.057). C-myc gain was found in 74 of 133 cases (55.6%) of NTs; no C-myc amplification or translocation was detected. Forty percent (6/15) of cases with N-myc amplification and 57.6% (68/118) of cases with N-myc non-amplification were accompanied by C-myc gain. The difference between N-myc amplification and non-amplification with C-myc gain was not significant (P > 0.05). Univariate analysis indicated that the outcome difference was not statistically significant between C-myc gain cases and normal C-myc cases (P = 0.357). CONCLUSIONS: The incidence of N-myc amplification only found in NB is low in pediatric NTs in China. Patients with N-myc amplification predict poorer outcome. No amplification or translocation of C-myc is detected in NTs, whereas C-myc gain is relatively common in NTs. There is no obvious association between N-myc amplification and C-myc gain. FAU - Cai, Rong-qin AU - Cai RQ AD - Department of Pathology, Basic Medical College, Capital Medical University, Beijing, China. FAU - Zhou, Chun-ju AU - Zhou CJ FAU - Sun, Qin-nuan AU - Sun QN FAU - Ma, Xiao-li AU - Ma XL FAU - Wang, Miao AU - Wang M FAU - Li, Yong AU - Li Y FAU - Wang, Da-ye AU - Wang DY FAU - Gong, Li-ping AU - Gong LP LA - chi PT - English Abstract PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - China TA - Zhonghua Bing Li Xue Za Zhi JT - Zhonghua bing li xue za zhi = Chinese journal of pathology JID - 0005331 SB - IM MH - Adrenal Gland Neoplasms/genetics/*pathology MH - Child MH - Child, Preschool MH - Female MH - Follow-Up Studies MH - Ganglioneuroblastoma/genetics/pathology MH - Ganglioneuroma/genetics/pathology MH - *Gene Amplification MH - *Genes, myc MH - Humans MH - In Situ Hybridization, Fluorescence MH - Infant MH - Male MH - Mediastinal Neoplasms/genetics/pathology MH - Neuroblastoma/genetics/*pathology MH - Survival Rate EDAT- 2013/09/06 06:00 MHDA- 2014/01/08 06:00 CRDT- 2013/09/06 06:00 PHST- 2013/09/06 06:00 [entrez] PHST- 2013/09/06 06:00 [pubmed] PHST- 2014/01/08 06:00 [medline] AID - 10.3760/cma.j.issn.0529-5807.2013.05.003 [doi] PST - ppublish SO - Zhonghua Bing Li Xue Za Zhi. 2013 May;42(5):299-304. doi: 10.3760/cma.j.issn.0529-5807.2013.05.003.