Zhang Qinyuan, Wu Wen, Guo Fanying, Li Jinming, Jin Yutao, Cai Guoxiang, Yang Yongzhi
Department of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China.
Microorganisms. 2024 Jun 28;12(7):1319. doi: 10.3390/microorganisms12071319.
Patients with colorectal cancer (CRC) have a high prevalence of iron deficiency anemia (IDA), and the gut microbiota is closely related to iron metabolism. We performed metagenomic and metabolomic analyses of stool samples from 558 eligible samples, including IDA CRC patients (IDA, n = 69), non-anemia CRC patients (Non-Anemia, n = 245), and healthy controls (CTRL, n = 244), to explore the dynamically altered gut microbes and their metabolites. Compared with the CTRL group, fecal bacteria in both the IDA group and the Non-Anemia group showed a decrease in alpha diversity and changes in microbial communities. () increases progressively from CTRL to Non-Anemia to IDA, accompanied by decreased trimethoxyflavanone and a downregulated KO gene, megDIII. In the Non-Anemia group, showed a specifically elevated abundance positively correlated with enriched 1,25-dihydroxyvitamin D3. The intricate correlations among gut microbiota, metabolites, and KO genes were uncovered and highlighted, implicating an aberrant iron metabolism vulnerable to chronic inflammation during the deterioration of the anemic condition. Furthermore, the amount of in feces achieved independent and effective prediction performance for the poor outcome of CRC. Perturbed host-microbe interplays represent a novel prospect for explaining the pathogenesis of CRC-associated IDA. The fecal microbial features also reflect the associations between IDA and elevated CRC recurrence risk.
结直肠癌(CRC)患者缺铁性贫血(IDA)的患病率很高,并且肠道微生物群与铁代谢密切相关。我们对558份合格样本的粪便样本进行了宏基因组和代谢组分析,这些样本包括IDA CRC患者(IDA,n = 69)、非贫血CRC患者(非贫血,n = 245)和健康对照(CTRL,n = 244),以探索动态变化的肠道微生物及其代谢产物。与CTRL组相比,IDA组和非贫血组的粪便细菌均显示出α多样性降低和微生物群落变化。()从CTRL到非贫血再到IDA逐渐增加,同时三甲氧基黄酮减少,KO基因megDIII下调。在非贫血组中,显示出丰度特异性升高,与富集的1,25 - 二羟基维生素D3呈正相关。揭示并强调了肠道微生物群、代谢产物和KO基因之间的复杂相关性,这意味着在贫血病情恶化期间,铁代谢异常易受慢性炎症影响。此外,粪便中的量对CRC的不良预后具有独立且有效的预测性能。宿主 - 微生物相互作用的紊乱为解释CRC相关IDA的发病机制提供了新的前景。粪便微生物特征也反映了IDA与CRC复发风险升高之间的关联。