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对爱尔兰海洋生物样本库进行筛选,发现一种新的苔藓抑素类似物是活化B细胞弥漫性大B细胞淋巴瘤的有效抑制剂。

Screening the Irish Marine Biorepository Identifies a New Bryostatin Analog as Potent Inhibitor of Activated B-Cells Diffuse Large B-Cell Lymphoma.

作者信息

Jennings Laurence K, Spriano Filippo, Reddy Maggie M, Cascione Luciano, Civanelli Elisa, Rinaldi Andrea, Bertoni Francesco, Thomas Olivier P

机构信息

School of Biological and Chemical Sciences, Ryan Institute, University of Galway, University Road, Galway, H91 TK33, Ireland.

Institute of Oncology Research, Faculty of Biomedical Sciences, USI, via F. Chiesa 5, 6500, Bellinzona, Switzerland.

出版信息

Chembiochem. 2025 Oct 3;26(19):e202500500. doi: 10.1002/cbic.202500500. Epub 2025 Sep 11.

Abstract

Activated B-cell diffuse large B-cell lymphoma (ABC-DLBCL) is an aggressive cancer with poor response to standard chemotherapy. In search of new therapeutic leads, a library of 435 fractions prepared from the Irish marine biorepository was screened against 2 ABC-DLBCL cell lines (TMD8 and OCI-Ly10) and a non-cancerous control cell line (CB33). Active fractions are prioritized based on potency and selectivity. Among them, fractions from the nudibranch Antiopella cristata and the ascidian Diplosoma listerianum exhibit the most potent and selective cytotoxicity. Bioassay-guided fractionation of D. listerianum led to the identification of the known loliolide and epiloliolide. On the other hand, A. cristata yielded several bryostatin analogs, including bryostatin 13 and a new natural product, its 18-demethylated analog. Both compounds demonstrated nanomolar cytotoxicity against ABC-DLBCL cell lines with minimal activity in CB33. Transcriptomic profiling showed significant gene expression changes, particularly for the 18-demethylated analog, implicating modulation of key signaling pathways. This study identifies A. cristata as a novel and highly enriched source of bioactive bryostatins and supports the dietary sequestration hypothesis in nudibranchs, highlighting the value of marine invertebrates as reservoirs of selective anticancer agents for drug discovery.

摘要

活化B细胞弥漫性大B细胞淋巴瘤(ABC-DLBCL)是一种侵袭性癌症,对标准化疗反应不佳。为了寻找新的治疗线索,对从爱尔兰海洋生物库中制备的435个馏分文库针对2种ABC-DLBCL细胞系(TMD8和OCI-Ly10)和一种非癌对照细胞系(CB33)进行了筛选。根据效力和选择性对活性馏分进行排序。其中,来自裸鳃亚目动物晶拟海牛和海鞘李氏双体海鞘的馏分表现出最强和最具选择性的细胞毒性。对李氏双体海鞘进行生物测定指导的分级分离,鉴定出了已知的洛利内酯和表洛利内酯。另一方面,晶拟海牛产生了几种苔藓抑素类似物,包括苔藓抑素13和一种新的天然产物,即其18-去甲基化类似物。这两种化合物对ABC-DLBCL细胞系均表现出纳摩尔级的细胞毒性,而对CB33细胞的活性最小。转录组分析显示基因表达有显著变化,特别是对于18-去甲基化类似物,这表明关键信号通路受到了调节。这项研究将晶拟海牛确定为生物活性苔藓抑素的一种新型且高度富集的来源,并支持了裸鳃亚目动物的饮食隔离假说,突出了海洋无脊椎动物作为药物发现中选择性抗癌剂储存库的价值。

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