成釉细胞瘤:最新分子病理发现综述。

Biomarkers in cancer Pub Date : 2015-10-04 eCollection Date: 2015-01-01 DOI:10.4137/BIC.S29329
Noah A Brown, Bryan L Betz
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引用次数: 79

摘要

成釉细胞瘤是一种牙源性肿瘤,其分子发病机制直到最近才被阐明。在绝大多数成釉细胞瘤中发现的FGFR2、BRAF和RAS的复发性激活突变暗示了MAPK通路信号失调是该肿瘤发病机制的关键步骤。关于影响sonic hedgehog (SHH)通路的突变,特别是Smoothened (SMO)的作用存在一定程度的争议,SMO被认为是另一种致病机制或继发性突变。在这里,我们回顾了我们对成釉细胞瘤分子发病机制的理解以及这些发现的诊断、预后和治疗意义的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Ameloblastoma: A Review of Recent Molecular Pathogenetic Discoveries.

Ameloblastoma is an odontogenic neoplasm whose molecular pathogenesis has only recently been elucidated. The discovery of recurrent activating mutations in FGFR2, BRAF, and RAS in a large majority of ameloblastomas has implicated dysregulation of MAPK pathway signaling as a critical step in the pathogenesis of this tumor. Some degree of controversy exists regarding the role of mutations affecting the sonic hedgehog (SHH) pathway, specifically Smoothened (SMO), which have been postulated to serve as either an alternative pathogenetic mechanism or secondary mutations. Here, we review recent advances in our understanding of the molecular pathogenesis of ameloblastoma as well as the diagnostic, prognostic, and therapeutic implications of these discoveries.

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