Enomoto H, Nakamura Y, Kondo K, Hirose M, Kaneko Y, Horie H, Takahashi H, Ohnuma N, Tanabe M, Nakagawara A
Department of Pediatric Surgery, School of Medicine, Chiba University, Japan.
J Pediatr Surg. 1998 Sep;33(9):1404-7. doi: 10.1016/s0022-3468(98)90019-7.
Molecular and biological analyses of a neuroblastoma case in which the original tumor contained a nodular region are described. No significant difference was observed between the nodular and the surrounding tumor tissue with respect to histopathologic examination, N-myc amplification, and trkA expression. However, flow cytometric analysis demonstrated that the nodular region consisted of a hypertetraploid clone, whereas the surrounding tissue mostly contained a hyperdiploid clone. Chromosome analysis showed that each clone had a similar chromosome acquisition pattern, suggesting that the hypertetraploid cells of the nodular region arose from the hyperdiploid cells of the surrounding tissue. Moreover, primary culture findings of the tumor cells showed that the responses to nerve growth factor or retinoic acid were different between the two. Collectively, this case suggests the possibility that neuroblastoma acquires novel biological characteristics through karyotypic evolution in vivo.
本文描述了一例神经母细胞瘤病例的分子和生物学分析,该病例的原发肿瘤包含一个结节区域。在组织病理学检查、N-myc基因扩增和trkA表达方面,结节区域与周围肿瘤组织之间未观察到显著差异。然而,流式细胞术分析表明,结节区域由一个超四倍体克隆组成,而周围组织主要包含一个超二倍体克隆。染色体分析显示,每个克隆具有相似的染色体获得模式,这表明结节区域的超四倍体细胞起源于周围组织的超二倍体细胞。此外,肿瘤细胞的原代培养结果表明,两者对神经生长因子或视黄酸的反应不同。总体而言,该病例提示神经母细胞瘤可能通过体内核型进化获得新的生物学特性。