TY - JOUR
T1 - Identification of the genetic and clinical characteristics of neuroblastomas using genome-wide analysis
AU - Uryu, Kumiko
AU - Nishimura, Riki
AU - Kataoka, Keisuke
AU - Sato, Yusuke
AU - Nakazawa, Atsuko
AU - Suzuki, Hiromichi
AU - Yoshida, Kenichi
AU - Seki, Masafumi
AU - Hiwatari, Mitsuteru
AU - Isobe, Tomoya
AU - Shiraishi, Yuichi
AU - Chiba, Kenichi
AU - Tanaka, Hiroko
AU - Miyano, Satoru
AU - Koh, Katsuyoshi
AU - Hanada, Ryoji
AU - Oka, Akira
AU - Hayashi, Yasuhide
AU - Ohira, Miki
AU - Kamijo, Takehiko
AU - Nagase, Hiroki
AU - Takimoto, Tetsuya
AU - Tajiri, Tatsuro
AU - Nakagawara, Akira
AU - Ogawa, Seishi
AU - Takita, Junko
N1 - Publisher Copyright:
© Uryu et al.
PY - 2017
Y1 - 2017
N2 - To provide better insight into the genetic signatures of neuroblastomas, we analyzed 500 neuroblastomas (included specimens from JNBSG) using targeteddeep sequencing for 10 neuroblastoma-related genes and SNP arrays analysis. ALK expression was evaluated using immunohistochemical analysis in 259 samples. Based on genetic alterations, the following 6 subgroups were identified: groups A (ALK abnormalities), B (other gene mutations), C (MYCN amplification), D (11q loss of heterozygosity [LOH]), E (at least 1 copy number variants), and F (no genetic changes). Groups A to D showed advanced disease and poor prognosis, whereas groups E and F showed excellent prognosis. Intriguingly, in group A, MYCN amplification was not a significant prognostic marker, while high ALK expression was a relevant indicator for prognosis (P = 0.033). Notably, the co-existence of MYCN amplification and 1p LOH, and the co-deletion of 3p and 11q were significant predictors of relapse (P = 0.043 and P = 0.040). Additionally, 6q/8p LOH and 17q gain were promising indicators of survival in patients older than 5 years, and 1p, 4p, and 11q LOH potentially contributed to outcome prediction in the intermediate-risk group. Our genetic overview clarifies the clinical impact of genetic signatures and aids in the better understanding of genetic basis of neuroblastoma.
AB - To provide better insight into the genetic signatures of neuroblastomas, we analyzed 500 neuroblastomas (included specimens from JNBSG) using targeteddeep sequencing for 10 neuroblastoma-related genes and SNP arrays analysis. ALK expression was evaluated using immunohistochemical analysis in 259 samples. Based on genetic alterations, the following 6 subgroups were identified: groups A (ALK abnormalities), B (other gene mutations), C (MYCN amplification), D (11q loss of heterozygosity [LOH]), E (at least 1 copy number variants), and F (no genetic changes). Groups A to D showed advanced disease and poor prognosis, whereas groups E and F showed excellent prognosis. Intriguingly, in group A, MYCN amplification was not a significant prognostic marker, while high ALK expression was a relevant indicator for prognosis (P = 0.033). Notably, the co-existence of MYCN amplification and 1p LOH, and the co-deletion of 3p and 11q were significant predictors of relapse (P = 0.043 and P = 0.040). Additionally, 6q/8p LOH and 17q gain were promising indicators of survival in patients older than 5 years, and 1p, 4p, and 11q LOH potentially contributed to outcome prediction in the intermediate-risk group. Our genetic overview clarifies the clinical impact of genetic signatures and aids in the better understanding of genetic basis of neuroblastoma.
KW - ALK
KW - ALK immunohistochemistry staining
KW - Copy number variants
KW - Japan neuroblastoma study group (JNBSG)
KW - Target amplicon deep sequencing
UR - https://www.scopus.com/pages/publications/85037379224
U2 - 10.18632/oncotarget.22495
DO - 10.18632/oncotarget.22495
M3 - 記事
C2 - 29296183
AN - SCOPUS:85037379224
SN - 1949-2553
VL - 8
SP - 107513
EP - 107529
JO - Oncotarget
JF - Oncotarget
IS - 64
ER -