Yoon Youngmin, Kim Gihyeon, Jeon Bu-Nam, Fang Sungsoon, Park Hansoo
Department of Biomedical Science and Engineering, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Korea.
Genome and Company, Pangyo-ro 255, Bundang-gu, Seoungnam 13486, Korea.
Cancers (Basel). 2021 Feb 25;13(5):957. doi: 10.3390/cancers13050957.
Colorectal cancer (CRC) is among the leading causes of cancer-related death in the world. The development of CRC is associated with smoking, diet, and microbial exposure. Previous studies have shown that dysbiosis of the gut microbiome affects cancer development, because it leads to inflammation and genotoxicity. Supplementation with specific microbiota induces anti-tumor effects by enhancing of anti-tumor immunity. Here, we observed that supplementation with either of two strains reduces tumor growth in MC38 colon carcinoma-bearing mice. Interestingly, only one strain boosted the efficacy of cancer therapeutics, including oxaliplatin and PD-1 blockade. Extensive immune profiling and transcriptomic analysis revealed that the boosting strain augments lymphocyte-mediated anti-cancer immunity. Our results suggest that supplementation with strains could potentially be used as a strategy to enhance the efficacy of CRC therapeutics.
结直肠癌(CRC)是全球癌症相关死亡的主要原因之一。CRC的发生与吸烟、饮食和微生物暴露有关。先前的研究表明,肠道微生物群失调会影响癌症发展,因为它会导致炎症和基因毒性。补充特定的微生物群可通过增强抗肿瘤免疫力诱导抗肿瘤作用。在此,我们观察到补充两种菌株中的任何一种均可减少荷MC38结肠癌小鼠的肿瘤生长。有趣的是,只有一种菌株增强了包括奥沙利铂和PD-1阻断在内的癌症治疗药物的疗效。广泛的免疫分析和转录组分析表明,增强作用的菌株增强了淋巴细胞介导的抗癌免疫力。我们的结果表明,补充这些菌株有可能作为一种提高CRC治疗疗效的策略。