遗传改变和生长因子在von Recklinghausen神经纤维瘤病发病中的作用。

Neurofibromatosis Pub Date : 1989-01-01
V M Riccardi
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引用次数: 0

摘要

本文综述了有关von Recklinghausen神经纤维瘤病(NF-1)发病机制的最新进展。在NF-1的分子生物学部分,重点是遗传连锁,并注意到产前诊断,肿瘤遗传学和动物模型。在关于生长因子和受体的部分,第一部分涉及神经纤维瘤病作为细胞相互作用的模型,特别是不典型增生与瘤变、细胞-细胞相互作用和“恶性循环”正反馈机制的问题;额外的元素集中在神经生长因子- β,雪旺细胞有丝分裂原和其他生长因子。在最后一部分,重点是分子生物学方面的进一步发展,但额外强调临床医生对NF-1及其NF和非NF替代品的许多表型特征的非常强烈的投入。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic alterations and growth factors in the pathogenesis of von Recklinghausen neurofibromatosis.

This paper is a summary review of recent developments with regard to the pathogenesis of von Recklinghausen neurofibromatosis, or NF-1. In the section on molecular biology of NF-1, the focus is on genetic linkage, with a note about prenatal diagnosis, tumor genetics and animal models. In the section on growth factors and receptors, the first element deals with neurofibromatosis as a model of cellular interaction, and particularly the issues of dysplasia versus neoplasia, cell-cell interactions and 'vicious cycle' positive feedback mechanisms; additional elements focus on nerve growth factor-beta, Schwann cell mitogens and other growth factors. In the last section, the focus is on further developments in terms of molecular biology, but with additional emphasis on the need for very intense input from the clinicians characterizing the many phenotypes of NF-1 and its NF and non-NF alternatives.

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