Berberine exerts anti-tumor activity in diffuse large B-cell lymphoma by modulating c-myc/CD47 axis

被引:31
|
作者
Ren, Shuai [1 ,2 ,3 ]
Cai, Yiqing [1 ,2 ,3 ]
Hu, Shunfeng [1 ,2 ,3 ]
Liu, Jiarui [1 ,2 ,3 ]
Zhao, Yi [1 ,2 ,3 ]
Ding, Mengfei [1 ,2 ,3 ]
Chen, Xiaomin [1 ,2 ,3 ]
Zhan, Linquan [1 ,2 ,3 ]
Zhou, Xiangxiang [1 ,2 ,3 ,4 ,5 ,6 ]
Wang, Xin [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Shandong Univ, Cheeloo Coll Med, Shandong Prov Hosp, Dept Hematol, 324,Jingwu Rd, Jinan 250021, Shandong, Peoples R China
[2] Shandong First Med Univ, Shandong Prov Hosp, Dept Hematol, Jinan 250021, Shandong, Peoples R China
[3] Shandong Univ, Sch Med, Jinan 250012, Shandong, Peoples R China
[4] Shandong Prov Engn Res Ctr Lymphoma, Jinan 250021, Shandong, Peoples R China
[5] Branch Natl Clin Res Ctr Hematol Dis, Jinan 250021, Shandong, Peoples R China
[6] Soochow Univ, Affiliated Hosp 1, Natl Clin Res Ctr Hematol Dis, Suzhou 251006, Peoples R China
基金
中国博士后科学基金;
关键词
Diffuse large B-cell lymphoma; Berberine; CD47; Phagocytosis; Immunochemotherapy; CD47; BLOCKADE; MEDIATED DESTRUCTION; COLORECTAL-CANCER; TARGETING CD47; RITUXIMAB; ANGIOGENESIS; PHAGOCYTOSIS; CARCINOMA; APOPTOSIS; PATHWAY;
D O I
10.1016/j.bcp.2021.114576
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Diffuse large B-cell lymphoma (DLBCL) is the most common subtype of non-Hodgkin lymphoma (NHL) with high clinical heterogeneity and poor prognosis. Immune escape mediated by CD47 overexpression contributes to the limited efficacy of rituximab, an anti-CD20 antibody, which indicates a target to improve the efficacy of DLBCL treatment. Here, we validated berberine, a natural compound, as a suppressor of CD47 and revealed the involved mechanism and biological function in DLBCL. Berberine downregulated the expression of CD47 in DLBCL at the transcriptional level by suppressing c-myc expression. Berberine-induced CD47 inhibition enhanced the phagocytosis of macrophages, thereby eliminating DLBCL cells in vitro and in vivo. Interestingly, berberine enhanced the efficiency of anti-CD47 antibody and rituximab-mediated phagocytosis. Moreover, a novel prognostic model based on the combination of CD47 and CD68, a biomarker of macrophages, was established in DLBCL. Our results highlighted for the first time that berberine could restore macrophage function in the tumor microenvironment, enhance rituximab-mediated phagocytosis and promote anti-CD47 antibody function via suppressing CD47 expression, which revealed a new anti-tumor mechanism of berberine and provided novel insights into the rituximab-based immunochemotherapy and CD47-targeted immunotherapy in DLBCL.
引用
收藏
页数:14
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