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KAT/3BP:一种对侵袭性B细胞淋巴瘤具有单一及联合活性的代谢靶向药物。

KAT/3BP: A Metabolism-Targeting Agent with Single and Combination Activity in Aggressive B-Cell Lymphomas.

作者信息

Tarantelli Chiara, Spriano Filippo, Civanelli Elisa, Aresu Luca, Risi Giorgia, Cannas Eleonora, Kayali Omar, Cascione Luciano, Arribas Alberto J, Stathis Anastasios, Ko Young H, Bertoni Francesco

机构信息

Institute of Oncology Research, Faculty of Biomedical Sciences, Università Della Svizzera Italiana, 6500 Bellinzona, Switzerland.

Department of Veterinary Sciences, University of Turin, 10095 Turin, Italy.

出版信息

Cancers (Basel). 2025 Jun 18;17(12):2034. doi: 10.3390/cancers17122034.

Abstract

BACKGROUND/OBJECTIVES: Reprogramming of the cellular metabolism is a hallmark of cancer, offering therapeutic opportunities to target cancer cell vulnerabilities for therapeutic purposes. 3-Bromopyruvate (3BP) is a small alkylating agent that functions as an anti-metabolite, targeting key substrates in cancer metabolism and demonstrating antitumor activity across multiple cancer types. However, unformulated 3BP is associated with significant toxicity. This study investigates the efficacy of KAT/3BP, a clinical derivative of 3BP currently in phase 1 trials for hepatocellular carcinoma, in preclinical lymphoma models.

RESULTS

, KAT/3BP exhibited cytotoxic activity across 12 lymphoma cell lines-including diffuse large B-cell lymphoma and mantle cell lymphoma-with a median IC of 3.7 μM. It also remained effective against lymphoma cell lines with acquired resistance to FDA-approved therapies. , treatment with KAT/3BP led to reduced tumor size in a syngeneic mouse model, with the combination of oral and intratumoral administration showing the greatest efficacy. Furthermore, KAT/3BP demonstrated synergistic activity when combined with standard lymphoma therapies such as bendamustine and R-CHOP.

CONCLUSIONS

Our findings highlight the potential of KAT/3BP as a novel therapeutic option, either as a single agent or in combination regimens, for treating lymphomas.

摘要

背景/目的:细胞代谢重编程是癌症的一个标志,为针对癌细胞脆弱性进行治疗提供了机会。3-溴丙酮酸(3BP)是一种小的烷基化剂,作为一种抗代谢物,靶向癌症代谢中的关键底物,并在多种癌症类型中显示出抗肿瘤活性。然而,未配制的3BP具有显著的毒性。本研究在临床前淋巴瘤模型中研究了KAT/3BP(3BP的一种临床衍生物,目前正处于肝细胞癌1期试验阶段)的疗效。

结果

KAT/3BP在12种淋巴瘤细胞系中表现出细胞毒性活性,包括弥漫性大B细胞淋巴瘤和套细胞淋巴瘤,中位IC为3.7μM。它对获得性抗FDA批准疗法耐药的淋巴瘤细胞系也仍然有效。在同基因小鼠模型中,用KAT/3BP治疗导致肿瘤大小减小,口服和瘤内给药联合使用显示出最大疗效。此外,KAT/3BP与苯达莫司汀和R-CHOP等标准淋巴瘤疗法联合使用时表现出协同活性。

结论

我们的研究结果突出了KAT/3BP作为一种新型治疗选择的潜力,无论是作为单一药物还是联合方案,用于治疗淋巴瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb91/12191035/86478ef9efaa/cancers-17-02034-g001.jpg

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