Brodeur G M
Children's Hospital of Philadelphia, U.S.A.
Eur J Cancer. 1995;31A(4):505-10. doi: 10.1016/0959-8049(95)00040-p.
Neuroblastomas demonstrate both clinical and biological heterogeneity. We have proposed that neuroblastomas may be classified in three genetically distinct subtypes, based on cytogenetic and molecular analysis. The first comprises those with hyperdiploid or triploid modal karyotypes (or compatible DNA content by flow cytometry), 1p LOH and MYCN amplification are absent, and TRKA expression is high. These patients are likely to be infants with low stages of disease (stages 1, 2, or 4S by the International Neuroblastoma Staging System), and they have a very favourable outcome (> 90% cure). The second group consists of tumours that generally have a near diploid or tetraploid modal chromosome number or DNA content but lack MYCN amplification. They usually have 1p allelic loss, 14q allelic loss or other structural changes, and TRKA expression is usually low. These patients are generally older with advanced stages of disease (stages 3 or 4), and they have a slowly progressive course, with a cure rate of 25-50%. The third group is characterised by tumours with MYCN amplification. These tumours are generally near diploid or tetraploid, with 1p allelic loss, and low or absent TRKA expression. The patients are usually between 1 and 5 years of age with advanced stages of disease, and they have a very poor prognosis (< 5%). It remains to be determined if tumours in one group ever evolve into a less unfavourable group, but current evidence suggests that they are distinct genetically. The identification of the oncogenes, suppressor genes and growth factor receptor pathways involved in neuroblastomas has provided great insight into the mechanisms of malignant transformation and progression, and ultimately they may provide the targets for future therapy.
神经母细胞瘤表现出临床和生物学异质性。我们提出,基于细胞遗传学和分子分析,神经母细胞瘤可分为三种基因上不同的亚型。第一种包括那些具有超二倍体或三倍体核型模式(或通过流式细胞术检测的兼容DNA含量)的肿瘤,不存在1p杂合性缺失和MYCN扩增,且TRKA表达高。这些患者可能是疾病分期较低的婴儿(根据国际神经母细胞瘤分期系统为1期、2期或4S期),他们的预后非常好(治愈率>90%)。第二组由通常具有近二倍体或四倍体核型数目或DNA含量但缺乏MYCN扩增的肿瘤组成。它们通常有1p等位基因缺失、14q等位基因缺失或其他结构改变,且TRKA表达通常较低。这些患者一般年龄较大,疾病分期较晚(3期或4期),病程进展缓慢,治愈率为25%-50%。第三组的特征是具有MYCN扩增的肿瘤。这些肿瘤通常接近二倍体或四倍体,有1p等位基因缺失,且TRKA表达低或无表达。患者通常年龄在1至5岁之间,疾病分期较晚,预后非常差(<5%)。一组中的肿瘤是否会演变为预后较好的组仍有待确定,但目前的证据表明它们在基因上是不同的。对神经母细胞瘤中涉及的癌基因、抑癌基因和生长因子受体途径的鉴定,为恶性转化和进展的机制提供了深刻见解,最终它们可能为未来的治疗提供靶点。