【24h】

Molecular Nevogenesis

机译:分子痣发生

获取原文
       

摘要

Despite recent advances, the biology underlying nevogenesis remains unclear. Activating mutations in NRAS, HRAS, BRAF, and GNAQ have been identified in benign nevi. Their presence roughly correlates with congenital, Spitz, acquired, and blue nevi, respectively. These mutations are likely to play a critical role in driving nevogenesis. While each mutation is able to activate the MAP kinase pathway, they also interact with a host of different proteins in other pathways. The different melanocytic developmental pathways activated by each mutation cause the cells to migrate, proliferate, and differentiate to different extents within the skin. This causes each mutation to give rise to a characteristic growth pattern. The exact location and differentiation state of the cell of origin for benign moles remains to be discovered. Further research is necessary to fully understand nevus development given that most of the same developmental pathways are also present in melanoma.
机译:尽管有最近的进展,但尚不清楚神经形成的生物学基础。在良性痣中已鉴定出NRAS,HRAS,BRAF和GNAQ中的激活突变。它们的存在分别与先天性,斯皮茨,后天性和蓝色痣相关。这些突变可能在驱动痣发生中起关键作用。尽管每个突变都能激活MAP激酶途径,但它们也与其他途径的许多不同蛋白质相互作用。每个突变激活的不同的黑素细胞发育途径导致细胞在皮肤内迁移,增殖和分化至不同程度。这导致每个突变产生特征性的生长模式。良性痣的起源细胞的确切位置和分化状态仍有待发现。鉴于大多数相同的发育途径也存在于黑色素瘤中,因此有必要进行进一步的研究以充分了解痣的发育。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号