QPH-FR: A Novel Quinoa Peptide Enhances Chemosensitivity by Targeting Leucine-Rich Repeat-Containing G Protein-Coupled Receptor 5 in Colorectal Cancer

被引:1
作者
Tian, Jinmiao [1 ]
Zhang, Lichao [2 ]
La, Xiaoqin [2 ]
An, Yuxuan [1 ]
Fan, Xiaxia [1 ]
Li, Zhuoyu [1 ]
机构
[1] Shanxi Univ, Inst Biotechnol, Key Lab Chem Biol & Mol Engn, Natl Minist Educ, Taiyuan 030006, Peoples R China
[2] Shanxi Univ, Inst Biomed Sci, Taiyuan 030006, Peoples R China
基金
中国国家自然科学基金;
关键词
quinoa; peptide; chemosensitivity; tumor stemness; LGR5; COLON-CANCER; STEM-CELLS; LGR5; EXPRESSION; ANTITUMOR;
D O I
10.1021/acs.jafc.4c03761
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Chemoresistance is one of the difficulties in the treatment of colorectal cancer (CRC), and the enhanced stemness of tumor cells is the underlying contributing factor. Leucine-rich repeat-containing G-protein-coupled receptor 5 (LGR5) is a classical marker of CRC stem cells and can be an important potential target for CRC chemotherapy. Quinoa, a protein-rich plant, offers potential as a source of high-quality active peptides. Novelly, the study obtained quinoa protein hydrolysate (QPH) from whole quinoa grains by simulated digestion. In vivo experiments revealed that the tumor volume in the 5-FU+QPH group decreased from 145.90 +/- 13.35 to 94.49 +/- 13.05 mm(3) in the 5-FU group, suggesting that QPH enhances the chemosensitivity of CRC. Further, the most effective peptide QPH-FR from 631 peptides in QPH was screened by activity prediction, molecular docking, and experimental validation. Mechanistically, QPH-FR competitively suppressed the formation of the LGR5/RSPO1 complex by binding to LGR5, causing RNF43/ZNRF3 to ubiquitinate the FZD receptor, thereby suppressing the Wnt/beta-catenin signaling pathway and exerting stemness inhibition. In summary, the study proposes that a novel peptide QPH-FR from quinoa elucidates the mechanism by which QPH-FR targets LGR5 to enhance chemosensitivity, providing theoretical support for the development of chemotherapeutic adjuvant drugs based on plant peptides.
引用
收藏
页码:17417 / 17430
页数:14
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