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FKBP3 通过 PARK7 介导的 Wnt/β-catenin 信号通路激活加重弥漫性大 B 细胞淋巴瘤的恶性表型。

FKBP3 aggravates the malignant phenotype of diffuse large B-cell lymphoma by PARK7-mediated activation of Wnt/β-catenin signalling.

机构信息

Department of Hematology and Breast Cancer, Cancer Hospital of Dalian University of Technology (Liaoning Cancer Hospital & Institute), Shenyang, China.

Department of Pathology, Shenyang Medical College, Shenyang, China.

出版信息

J Cell Mol Med. 2024 Jan;28(1):e18041. doi: 10.1111/jcmm.18041. Epub 2023 Nov 21.

Abstract

Diffuse large B-cell lymphoma (DLBCL) is difficult to treat due to the high recurrence rate and therapy intolerance, so finding potential therapeutic targets for DLBCL is critical. FK506-binding protein 3 (FKBP3) contributes to the progression of various cancers and is highly expressed in DLBCL, but the role of FKBP3 in DLBCL and its mechanism are not clear. Our study demonstrated that FKBP3 aggravated the proliferation and stemness of DLBCL cells, and tumour growth in a xenograft mouse model. The interaction between FKBP3 and parkinsonism associated deglycase (PARK7) in DB cells was found using co-immunoprecipitation assay. Knockdown of FKBP3 enhanced the degradation of PARK7 through increasing its ubiquitination modification. Forkhead Box O3 (FOXO3) belongs to the forkhead family of transcription factors and inhibits DLBCL, but the underlying mechanism has not been reported. We found that FOXO3 bound the promoter of FKBP3 and then suppressed its transcription, eventually weakening DLBCL. Mechanically, FKBP3 activated Wnt/β-catenin signalling pathway mediated by PARK7. Together, FKBP3 increased PARK7 and then facilitated the malignant phenotype of DLBCL through activating Wnt/β-catenin pathway. These results indicated that FKBP3 might be a potential therapeutic target for the treatment of DLBCL.

摘要

弥漫性大 B 细胞淋巴瘤(DLBCL)由于复发率高和治疗不耐受,治疗困难,因此寻找 DLBCL 的潜在治疗靶点至关重要。FK506 结合蛋白 3(FKBP3)促进了多种癌症的进展,在 DLBCL 中高表达,但 FKBP3 在 DLBCL 中的作用及其机制尚不清楚。我们的研究表明,FKBP3 加重了 DLBCL 细胞的增殖和干性,并在异种移植小鼠模型中促进了肿瘤生长。通过免疫共沉淀实验发现 FKBP3 与 PARK7 在 DLBCL 细胞中相互作用。FKBP3 的敲低通过增加其泛素化修饰来增强 PARK7 的降解。叉头框 O3(FOXO3)属于转录因子叉头家族,可抑制 DLBCL,但尚未报道其潜在机制。我们发现 FOXO3 结合 FKBP3 的启动子,从而抑制其转录,最终减弱 DLBCL。机制上,FKBP3 通过 PARK7 激活 Wnt/β-catenin 信号通路。总之,FKBP3 通过激活 Wnt/β-catenin 通路增加 PARK7,从而促进 DLBCL 的恶性表型。这些结果表明 FKBP3 可能是治疗 DLBCL 的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f903/10805489/f6380b424e8c/JCMM-28-e18041-g004.jpg

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