Endocrinology and Diabetes Group, School of Biomedicine, Manchester Academic Health Sciences Centre, University of Manchester, Manchester M13 9PT, UK.
Trends Mol Med. 2011 Mar;17(3):166-74. doi: 10.1016/j.molmed.2010.12.001. Epub 2011 Jan 13.
The transcription factor SOX9 is crucial for multiple aspects of development. Mutations in SOX9 cause campomelic dysplasia, a haploinsufficiency disorder concordant with the expression profile of SOX9 during embryogenesis. The mechanistic understanding of development has revealed roles for SOX9 in regulating cartilage extracellular matrix (ECM) production and cell proliferation, among others. More recently, it transpires that SOX9 becomes expressed and induces destructive ECM components in organ fibrosis and related disorders. Although commonly absent from the parent cell type, SOX9 is expressed in a wide range of cancers, where it regulates cell proliferation. These data have potential diagnostic, prognostic and therapeutic relevance, suggesting that disease mechanisms might result from re-expressing this developmental transcription factor in ectopic locations.
转录因子 SOX9 对于多个发育方面至关重要。SOX9 基因突变导致 Campomelic 发育不良,这是一种与 SOX9 在胚胎发生过程中的表达谱一致的单倍体不足障碍。对发育机制的理解揭示了 SOX9 在调节软骨细胞外基质 (ECM) 产生和细胞增殖等方面的作用。最近,SOX9 在器官纤维化和相关疾病中的表达并诱导破坏性 ECM 成分的事实浮出水面。尽管通常不存在于亲本细胞类型中,但 SOX9 在广泛的癌症中表达,在这些癌症中它调节细胞增殖。这些数据具有潜在的诊断、预后和治疗相关性,表明疾病机制可能源于异位重新表达这种发育转录因子。