Looijenga Leendert H J, Gillis Ad J M, Stoop Hans J, Hersmus Remko, Oosterhuis J Wolter
Department of Pathology, Josephine Nefkens Institute, Erasmus MC-University Medical Center Rotterdam, Daniel den Hoed Cancer Center, Rotterdam, The Netherlands.
Ann N Y Acad Sci. 2007 Dec;1120:187-214. doi: 10.1196/annals.1411.000. Epub 2007 Oct 2.
Human germ-cell tumors (GCTs) are a heterogeneous group of neoplasms. Based on epidemiology, anatomical site of presentation, histology, chromosomal constitution, and pattern of genomic imprinting, GCTs are classified into five entities. Within the testis, three types of GCTs can be diagnosed: type I (teratomas and yolk-sac tumors of neonates and infants); type II (seminomas and nonseminomas); type III (spermatocytic seminomas). Here the focus is on the type II GCTs, the most frequent type in the adult testis (so-called TGCTs). They can also be diagnosed in dysgenetic gonads (an incomplete or defective formation of the gonad, caused by a disturbed process of migration of the germ cells and/or their correct organization in their fetal gonadal ridge), the anterior mediastinum, and pineal/suprasellar region. In the testis, they originate from the malignant counterpart of primordial germ cells/gonocytes, referred to as carcinoma in situ (CIS)/intratubular germ-cell neoplasia unclassified (ITGCNU). CIS/ITGCNU and seminomatous cells are characterized by expression of OCT3/4 and NANOG, while in addition embryonal carcinoma expresses SOX2, all identified as transcription factors related to pluripotency in embryonic stem (ES) cells. With the exception of teratomas, most histological elements of TGCTs are sensitive for (cisplatin-based) chemotherapy; CIS/ITGCNU and seminoma cells are also sensitive to DNA damage induced by irradiation. Similar observations have been made for ES cells and their derivates. Moreover, the genetic constitution of TGCTs (low incidence of mutations and frequent uniparental disomies) can also be linked to characteristics of ES cells, likely related to their specific inability to repair DNA damage and their high sensitivity to apoptotic cell death. The unusual presence of wild-type P53 in TGCTs is explained by specific expression of a cluster of micro-RNAs (miRNAs), that is, hsa-miR 371-373, also expressed in ES cells, which prevents P53-driven cellular senescence upon oncogenic stress. Many characteristics of human TGCTs reflect the nonmalignant counterparts from which they originate. Demonstration of these characteristics, in combination with the knowledge of the abnormal niche of these cells, normally occupied by spermatogonia, allows an informative method for (early) diagnosis. The conclusion is that TGCTs are embryonic cancers found in adults.
人类生殖细胞肿瘤(GCTs)是一组异质性肿瘤。根据流行病学、临床表现的解剖部位、组织学、染色体构成以及基因组印记模式,GCTs可分为五个实体。在睾丸内,可诊断出三种类型的GCTs:I型(新生儿和婴儿的畸胎瘤和卵黄囊瘤);II型(精原细胞瘤和非精原细胞瘤);III型(精母细胞性精原细胞瘤)。这里重点关注II型GCTs,它是成人睾丸中最常见的类型(所谓的睾丸生殖细胞肿瘤,TGCTs)。它们也可在发育异常的性腺(生殖细胞迁移过程紊乱和/或其在胎儿性腺嵴中正确组织形成过程受到干扰导致的性腺不完全或有缺陷形成)、前纵隔以及松果体/鞍上区域被诊断出来。在睾丸中,它们起源于原始生殖细胞/生殖母细胞的恶性对应物,称为原位癌(CIS)/未分类的管内生殖细胞肿瘤(ITGCNU)。CIS/ITGCNU和精原细胞瘤细胞的特征是表达OCT3/4和NANOG,而胚胎癌还表达SOX2,所有这些都被鉴定为与胚胎干细胞(ES细胞)多能性相关的转录因子。除了畸胎瘤外,TGCTs的大多数组织学成分对(基于顺铂的)化疗敏感;CIS/ITGCNU和精原细胞瘤细胞对辐射诱导的DNA损伤也敏感。对ES细胞及其衍生物也有类似的观察结果。此外,TGCTs的基因构成(突变发生率低且单亲二体频繁)也可与ES细胞的特征相关联,这可能与其修复DNA损伤的特定能力缺陷以及对凋亡性细胞死亡的高敏感性有关。TGCTs中野生型P53的异常存在是由一组微小RNA(miRNA),即hsa-miR 371 - 373的特异性表达所解释的,它们也在ES细胞中表达,可在致癌应激时阻止P53驱动的细胞衰老。人类TGCTs的许多特征反映了它们起源的非恶性对应物。这些特征的证明,结合对这些细胞通常由精原细胞占据的异常微环境的了解,为(早期)诊断提供了一种有用的方法。结论是TGCTs是在成人中发现的胚胎性癌症。