The role of SPRED1 mutation in melanoma

SPRED1突变在黑色素瘤中的作用

阅读:2

Abstract

Melanoma is a highly malignant tumor, with its initiation and progression tightly linked to the aberrant activation of the MAPK signaling pathway. As a critical negative regulator of the MAPK pathway, SPRED1 frequently exhibits genomic alteration in melanoma, including gene deletions and mutations, which lead to its functional inactivation. Consequently, the loss of SPRED1-mediated inhibition on the MAPK pathway significantly drives tumorigenesis and progression, enhances invasive and metastatic capacities, and is closely associated with therapeutic resistance. This article systematically reviews the structure and biological functions of SPRED1, its mutation profiles across different melanoma subtypes, and its regulatory mechanisms on the MAPK pathway. Furthermore, it discusses the associations of SPRED1 alteration with tumor malignant progression, as well as resistance to targeted therapy and immunotherapy. This review aims to provide a comprehensive theoretical basis for the precise diagnosis, treatment, and fundamental research of melanoma.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。