作者: Gergana Metodieva , Naiara Correa Nogueira-de-Souza , Christina Greenwood , Khalid Al-Janabi , Lin Leng
DOI: 10.1593/NEO.13464
关键词: Molecular biology 、 Major histocompatibility complex 、 Tumor suppressor gene 、 CD74 、 Cell culture 、 Antigen 、 Cancer research 、 Phosphorylation 、 Regulation of gene expression 、 Biology 、 Cancer cell
摘要: The γ subunit of the major histocompatibility complex (MHC) class II complex, CD74, is overexpressed in a significant proportion metastatic breast tumors, but mechanistic foundation and biologic significance this phenomenon are not fully understood. Here, we show that when CD74 human cancer noncancerous epithelial cells, it interacts interferes with function Scribble, product well-known tumor suppressor gene. Furthermore, using cell lines expressing under control tetracycline-inducible promoter quantitative high-resolution mass spectrometry, demonstrate that, as result overexpression, phosphorylation pattern C-terminal part Scribble undergoes specific changes. This accompanied translocation protein from sites cell-to-cell contacts at plasma membrane to cytoplasm, which likely effectively enhance motility invasiveness cells.