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DS0709对结直肠癌的凋亡诱导作用

Apoptosis-Inducing Effects of DS0709 in Colorectal Cancer.

作者信息

Tae In Hwan, Kang Yunsang, Lee Jinkwon, Lee Jeongmin, Kim Jinsan, Yang Haneol, Park Kunhyang, Park Doo-Sang, Kim Dae-Soo, Cho Hyun-Soo

机构信息

Korea Research Institute of Bioscience and Biotechnology, Daejeon 34141, Republic of Korea.

Korea University of Science and Technology, Daejeon 34113, Republic of Korea.

出版信息

J Microbiol Biotechnol. 2025 Aug 15;35:e2504042. doi: 10.4014/jmb.2504.04042.

Abstract

In colorectal cancer (CRC) treatment, various approaches, including chemotherapy (5-FU, irinotecan, and oxaliplatin), targeted therapy (VEGF inhibitor) and immunotherapy (PD-1/ PD-L1 inhibitor), are employed. However, due to side effects and limited efficacy, more effective novel therapeutic strategies have been required. In this study, we identified the anti-cancer effects of DS0709, isolated from infant feces, on CRC. Treatment with the supernatant (Sup) of DS0709 demonstrated growth inhibition of CRC cell lines (HCT116 and SNUC5) by inducing apoptosis. Additionally, using human iPSC-derived intestinal organoids (hIO), we confirmed that DS0709 Sup exhibited no toxicity. Furthermore, in a 3D spheroid model mimicking conditions, DS0709 Sup showed similar apoptosis induction and growth-inhibitory effects as in 2D cultures. Thus, these findings suggest that DS0709 has the potential to be developed into a novel microbiome-based therapeutic agent for CRC, offering anti-cancer efficacy without side effects.

摘要

在结直肠癌(CRC)治疗中,采用了多种方法,包括化疗(5-氟尿嘧啶、伊立替康和奥沙利铂)、靶向治疗(VEGF抑制剂)和免疫治疗(PD-1/PD-L1抑制剂)。然而,由于副作用和疗效有限,需要更有效的新型治疗策略。在本研究中,我们鉴定了从婴儿粪便中分离出的DS0709对CRC的抗癌作用。用DS0709的上清液(Sup)处理可通过诱导凋亡来抑制CRC细胞系(HCT116和SNUC5)的生长。此外,使用人诱导多能干细胞衍生的肠道类器官(hIO),我们证实DS0709 Sup没有毒性。此外,在模拟条件的3D球体模型中,DS0709 Sup显示出与2D培养中相似的凋亡诱导和生长抑制作用。因此,这些发现表明DS0709有潜力被开发成一种基于微生物群的新型CRC治疗药物,具有抗癌疗效且无副作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fd8/12375538/f96deab5e74b/jmb-35-e2504042-f1.jpg

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