Alhhazmi Areej A, Almutawif Yahya A, Mumena Walaa A, Alhazmi Shaima M, Abujamel Turki S, Alhusayni Ruba M, Aloufi Raghad, Al-Hejaili Razan R, Alhujaily Rahaf, Alrehaili Lama M, Alsaedy Ruya A, Khoja Rahaf H, Ahmed Wassal, Abdelmohsen Mohamed F, Mohammed-Saeid Waleed
Medical Laboratories Technology Department, College of Applied Medical Sciences, Taibah University, Al-Madinah Al-Munawarah 42353, Saudi Arabia.
Clinical Nutrition Department, College of Applied Medical Sciences, Taibah University, Al-Madinah Al-Munawarah 42353, Saudi Arabia.
Cancers (Basel). 2023 Oct 17;15(20):5019. doi: 10.3390/cancers15205019.
Colorectal cancer (CRC) is a significant global health concern. Microbial dysbiosis and associated metabolites have been associated with CRC occurrence and progression. This study aims to analyze the gut microbiota composition and the enriched metabolic pathways in patients with late-stage CRC. In this study, a cohort of 25 CRC patients diagnosed at late stage III and IV and 25 healthy participants were enrolled. The fecal bacterial composition was investigated using V3-V4 ribosomal RNA gene sequencing, followed by clustering and linear discriminant analysis (LDA) effect size (LEfSe) analyses. A cluster of ortholog genes' (COG) functional annotations and the Kyoto Encyclopedia of Genes and Genomes (KEGG) were employed to identify enrichment pathways between the two groups. The findings showed that the fecal microbiota between the two groups varied significantly in alpha and beta diversities. CRC patients' fecal samples had significantly enriched populations of , , , , , , , , Family XIII_AD3001 Group, , , , , , , and (Q < 0.05). The enriched pathways identified in the CRC group were amino acid transport, signaling and metabolism, membrane biogenesis, DNA replication and mismatch repair system, and protease activity (Q < 0.05). These results suggested that the imbalance between intestinal bacteria and the elevated level of the predicated functions and pathways may contribute to the development of advanced CRC tumors. Further research is warranted to elucidate the exact role of the gut microbiome in CRC and its potential implications for use in diagnostic, prevention, and treatment strategies.
结直肠癌(CRC)是一个重大的全球健康问题。微生物群落失调及相关代谢产物与CRC的发生和发展有关。本研究旨在分析晚期CRC患者的肠道微生物群组成及富集的代谢途径。在本研究中,纳入了25例诊断为晚期III期和IV期的CRC患者及25名健康参与者。采用V3-V4核糖体RNA基因测序研究粪便细菌组成,随后进行聚类和线性判别分析(LDA)效应大小(LEfSe)分析。利用直系同源基因簇(COG)功能注释和京都基因与基因组百科全书(KEGG)来确定两组之间的富集途径。结果显示,两组之间的粪便微生物群在α和β多样性方面存在显著差异。CRC患者的粪便样本中, 、 、 、 、 、 、 、XIII_AD3001科菌群、 、 、 、 、 、 等菌的数量显著富集(Q < 0.05)。CRC组中鉴定出的富集途径包括氨基酸转运、信号传导和代谢、膜生物合成、DNA复制和错配修复系统以及蛋白酶活性(Q < 0.05)。这些结果表明,肠道细菌之间的失衡以及预测功能和途径水平的升高可能有助于晚期CRC肿瘤的发展。有必要进一步研究以阐明肠道微生物群在CRC中的确切作用及其在诊断、预防和治疗策略中的潜在意义。