Jiang Meizhi, Huang Fangfang, Hong Xiuli, Xu Chenyu, Zhang Bin, Hu Shengwei, Wang Guijiang, Hu Die, Sun Wenxin, Lu Quanyi, Liu Huiheng, Cai Dachuan, Yang Xianwen, Lin Ting, Chen Siming
Fujian Provincial Key Laboratory of Innovative Drug Target Research, School of Pharmaceutical Sciences, Xiamen University, Xiamen, China.
Department of Hematology, School of Medicine, Zhongshan Hospital, Xiamen University, Xiamen, China.
Chem Biodivers. 2025 Jul;22(7):e202500198. doi: 10.1002/cbdv.202500198. Epub 2025 Mar 23.
Polycomb repressive complex 2 (PRC2) is a multi-subunit complex that catalyzes the tri-methylation of histone H3 at lysine 27 (H3K27me3), serving as an epigenetic marker of gene silencing. PRC2 plays a crucial role in numerous fundamental biological processes, and its dysregulation is closely linked to cancer and developmental disorders. EZH2, a key component of PRC2, is aberrantly overexpressed in various human cancers. Inhibition of EZH2 enzymatic activity has been shown to effectively reduce cancer cell proliferation and tumorigenesis. Consequently, EZH2 is widely recognized as a driver of cancer, and the development of EZH2-specific inhibitors has become an active area of research. In this study, we screened over 2000 compounds from solid libraries using a PRC2 enzymatic activity assay and identified pyrroloquinoline quinone (PQQ) as a potent inhibitor of PRC2 methyltransferase activity in vitro. We evaluated the antitumor effects of PQQ across different tumor cell lines and found that it exhibited strong anticancer activity, specifically against B-cell lymphoma cells, which demonstrate elevated EZH2 activity. We used a combination of biochemical assays, cellular assays, and molecular docking studies to thoroughly investigate the inhibitory effects of PQQ on PRC2 activity. Furthermore, PQQ is a naturally occurring compound with various biological activities, including antioxidant and neuroprotective effects, and it has been approved as a nutritional supplement and health product in the United States. This study demonstrates, for the first time, that PQQ, a dietary supplement, selectively inhibits PRC2 methyltransferase activity, therefore providing new insights for targeted anti-lymphoma therapies involving PRC2.
多梳抑制复合物2(PRC2)是一种多亚基复合物,可催化组蛋白H3赖氨酸27位的三甲基化(H3K27me3),作为基因沉默的表观遗传标记。PRC2在众多基本生物学过程中发挥着关键作用,其失调与癌症和发育障碍密切相关。EZH2是PRC2的关键组成部分,在各种人类癌症中异常过表达。抑制EZH2酶活性已被证明可有效降低癌细胞增殖和肿瘤发生。因此,EZH2被广泛认为是癌症的驱动因素,开发EZH2特异性抑制剂已成为一个活跃的研究领域。在本研究中,我们使用PRC2酶活性测定法从固体文库中筛选了2000多种化合物,并确定吡咯并喹啉醌(PQQ)是一种在体外有效抑制PRC2甲基转移酶活性的抑制剂。我们评估了PQQ对不同肿瘤细胞系的抗肿瘤作用,发现它表现出强大的抗癌活性,特别是对EZH2活性升高的B细胞淋巴瘤细胞。我们结合生化测定、细胞测定和分子对接研究,全面研究了PQQ对PRC2活性的抑制作用。此外,PQQ是一种天然存在的化合物,具有多种生物活性,包括抗氧化和神经保护作用,并且已在美国被批准为营养补充剂和保健品。本研究首次证明,作为膳食补充剂的PQQ选择性抑制PRC2甲基转移酶活性,因此为涉及PRC2的靶向抗淋巴瘤治疗提供了新的见解。