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胚胎性中枢神经上皮肿瘤:当前概念与未来挑战

Embryonal central neuroepithelial tumors: current concepts and future challenges.

作者信息

Vandenberg S R, Herman M M, Rubinstein L J

出版信息

Cancer Metastasis Rev. 1987;5(4):343-65. doi: 10.1007/BF00055377.

Abstract

While the embryonal central neuroepithelial tumors present complex conceptual and clinical problems, advances in cell type identification by special neurohistological, immunohisto- and immunocytochemical techniques have permitted discrimination of distinct cytomorphogenetic entities. These are based in part on their resemblance to the normal phases of neurocytogenesis. Four of these tumors, medulloepithelioma, desmoplastic infantile ganglioglioma, pineoblastoma and medulloblastoma, are designated as multipotential in light of their capacity to undergo divergent differentiation. Cytomorphogenetic, clinical and experimental data implicate fetal neural cell targets for transformation and raise the possibility that aberrant developmental regulatory mechanisms may contribute to the biologic behavior of these tumors. Growth factors and some neuroregulatory neurotransmitters (such as serotonin) are known to act as modulators of normal neuromorphogenesis. They could play a regulatory role in central neuroepithelial tumors on the hypothesis that the aberrant behavior of the embryonal neoplasms could either be modified by functional receptor responses or result from abnormal receptor responses to these substances. Future challenges include the definition of new cytomorphogenetic entities and subgroups of the currently defined forms of embryonal CNS tumors based on the presence of specific growth factors and neuroregulatory neurotransmitters, or their receptors, the characterization of neoplastic receptor responses mediating any modulatory role of the presently known growth factors or neuroregulatory neurotransmitters on the growth and maturation potential of the embryonal central neuroepithelial tumors and the further definition of developmental, stage-specific modulators that might be operative in these tumors.

摘要

虽然胚胎性中枢神经上皮肿瘤存在复杂的概念和临床问题,但通过特殊神经组织学、免疫组织化学和免疫细胞化学技术进行细胞类型鉴定方面的进展,已能够区分不同的细胞形态发生实体。这些实体部分基于它们与神经细胞发生正常阶段的相似性。鉴于这四种肿瘤,即髓上皮瘤、促结缔组织增生性婴儿型神经节胶质瘤、松果体母细胞瘤和髓母细胞瘤具有进行不同分化的能力,故被指定为多潜能肿瘤。细胞形态发生、临床和实验数据表明,胎儿神经细胞是转化的靶点,并增加了异常发育调节机制可能促成这些肿瘤生物学行为的可能性。已知生长因子和一些神经调节性神经递质(如5-羟色胺)可作为正常神经形态发生的调节因子。基于胚胎性肿瘤的异常行为可能通过功能性受体反应得到改变或由对这些物质的异常受体反应所致这一假设,它们可能在中枢神经上皮肿瘤中发挥调节作用。未来的挑战包括根据特定生长因子和神经调节性神经递质或其受体的存在,定义新的细胞形态发生实体和当前定义的胚胎性中枢神经系统肿瘤形式的亚组;表征介导目前已知生长因子或神经调节性神经递质对胚胎性中枢神经上皮肿瘤生长和成熟潜能的任何调节作用的肿瘤受体反应;以及进一步定义可能在这些肿瘤中起作用的发育阶段特异性调节因子。

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