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[甲状腺上皮肿瘤的起源与进展:分子与细胞机制]

[Origin and progression of thyroid epithelial tumors: molecular and cellular mechanisms].

作者信息

Gire V, Wynford-Thomas D

机构信息

Department of Pathology, University of Wales College of Medicine, Cardiff, U.K.

出版信息

Arch Anat Cytol Pathol. 1998;46(1-2):11-8.

PMID:9754356
Abstract

Tumours of the thyroid follicular cell have been intensively studied as a model for investigating the molecular genetics of tumour development in epithelial cells. This review summarises the abnormalities of oncogenes and tumour suppressor genes which have been associated with the major sub-types of thyroid tumour. Although inevitably incomplete, the available data demonstrate well how successive genetic abnormalities drive clonal progression. Comparison of follicular and papillary tumours also reveals a fascinating correlation between genotype and pathological behaviour, consistent with a determining influence of the initiating oncogene on the "route" of tumour development. Finally, the emerging clinical implications are discussed.

摘要

甲状腺滤泡细胞肿瘤作为研究上皮细胞肿瘤发生分子遗传学的模型,已得到深入研究。本综述总结了与甲状腺肿瘤主要亚型相关的癌基因和肿瘤抑制基因的异常情况。尽管现有数据不可避免地不完整,但很好地展示了连续的基因异常如何驱动克隆进展。滤泡性肿瘤和乳头状肿瘤的比较还揭示了基因型与病理行为之间迷人的相关性,这与起始癌基因对肿瘤发展“路径”的决定性影响一致。最后,讨论了新出现的临床意义。

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