| Literature DB >> 34626540 |
Weixiang Bian1, Mengfan Tang2, Hua Jiang1, Wenyan Xu3, Wanyu Hao4, Yue Sui1, Yingnan Hou1, Litong Nie2, Huimin Zhang2, Chao Wang2, Nan Li2, Jiadong Wang5, Jun Qin6, Lianfeng Wu7, Xianjue Ma8, Junjie Chen9, Wenqi Wang10, Xu Li11.
Abstract
The Notch signaling pathway controls cell growth, differentiation, and fate decisions, and its dysregulation has been linked to various human genetic disorders and cancers. To comprehensively understand the global organization of the Notch pathway and identify potential drug targets for Notch-related diseases, we established a protein interaction landscape for the human Notch pathway. By combining and analyzing genetic and phenotypic data with bioinformatics analysis, we greatly expanded this pathway and identified many key regulators, including low-density-lipoprotein-receptor-related protein 1 (LRP1). We demonstrated that LRP1 mediates the ubiquitination chain linkage switching of Delta ligands, which further affects ligand recycling, membrane localization, and stability. LRP1 inhibition led to Notch signaling inhibition and decreased tumorigenesis in leukemia models. Our study provides a glimpse into the Notch pathway interaction network and uncovers LRP1 as one critical regulator of the Notch pathway, as well as a possible therapeutic target for Notch-related cancers.Entities:
Keywords: DLL3; LRP1; Notch pathway; interaction network; leukemia
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Year: 2021 PMID: 34626540 DOI: 10.1016/j.devcel.2021.09.015
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270