Heng Ding, Zhang Min, Yuan Yuhan, Qiu Xinyun
Department of Gastroenterology, The First Affiliated Hospital of Nanjing Medical University, No. 300, Guangzhou Road, Nanjing 210029, China.
Department of Endoscopic Center, The First Affiliated Hospital of Nanjing Medical University, No. 300, Guangzhou Road, Nanjing 210029, China.
Microorganisms. 2023 May 18;11(5):1327. doi: 10.3390/microorganisms11051327.
Colorectal cancer (CRC) develops from pre-cancerous cellular lesions in the gut epithelium and mainly originates from specific types of colonic adenomas with dysplasia. However, gut microbiota signatures among sampling sites in patients with colorectal adenomas with low-grade dysplasia (ALGD) and normal control (NC) remain uncharacterized. To characterize gut microbial and fungal profiles in ALGD and normal colorectal mucosa tissues. We used and gene sequencing and bioinformatics analysis on the microbiota of ALGD and normal colorectal mucosa from 40 subjects. Bacterial sequences in the ALGD group showed an increase in , and several genera, including , and compared to the NC group. Fungal sequences in the ALGD group showed an increase in , and , while several orders, families, and genera, including , and were decreased. The study found various interactions between intestinal bacteria and fungi. The bacterial functional analysis showed increased glycogen and vanillin degradation pathways in the ALGD group. Meanwhile, the fungal functional analysis showed a decrease in pathways related to the biosynthesis of gondoate and stearate, as well as degradation of glucose, starch, glycogen, sucrose, L-tryptophan, and pantothenate, and an increase in the octane oxidation pathway in the ALGD group. The mucosal microbiota in ALGD exhibits altered fungal and microbial composition compared to the NC mucosa, potentially contributing to the development of intestinal cancer by regulating specific metabolic pathways. Therefore, these changes in microbiota and metabolic pathways may be potential markers for diagnosing and treating colorectal adenoma and carcinoma.
结直肠癌(CRC)由肠道上皮中的癌前细胞病变发展而来,主要起源于具有发育异常的特定类型的结肠腺瘤。然而,低级别发育异常的结肠腺瘤(ALGD)患者与正常对照(NC)的不同采样部位之间的肠道微生物群特征仍未明确。为了明确ALGD和正常结直肠黏膜组织中的肠道微生物和真菌谱。我们对40名受试者的ALGD和正常结直肠黏膜微生物群进行了16S和ITS基因测序及生物信息学分析。与NC组相比,ALGD组的细菌序列显示出 、以及包括 、 和 在内的几个属的增加。ALGD组的真菌序列显示出 、以及 的增加,而包括 、 和 在内的几个目、科和属减少。该研究发现了肠道细菌和真菌之间的各种相互作用。细菌功能分析显示ALGD组中糖原和香草醛降解途径增加。同时,真菌功能分析显示ALGD组中与贡多酸和硬脂酸生物合成相关的途径减少,以及葡萄糖、淀粉、糖原、蔗糖、L-色氨酸和泛酸的降解减少,而辛烷氧化途径增加。与NC黏膜相比,ALGD中的黏膜微生物群表现出真菌和微生物组成的改变,可能通过调节特定代谢途径促进肠道癌症的发展。因此,微生物群和代谢途径的这些变化可能是诊断和治疗结肠腺瘤和癌的潜在标志物。