Messaritakis Ippokratis, Koulouris Andreas, Boukla Eleni, Vogiatzoglou Konstantinos, Lagkouvardos Ilias, Intze Evangelia, Sfakianaki Maria, Chondrozoumaki Maria, Karagianni Michaela, Athanasakis Elias, Xynos Evangelos, Tsiaoussis John, Christodoulakis Manousos, Flamourakis Matthaios E, Tsagkataki Eleni S, Giannikaki Linda, Chliara Evdoxia, Mavroudis Dimitrios, Tzardi Maria, Souglakos John
Laboratory of Translational Oncology, Medical School, University of Crete, 70013 Heraklion, Greece.
Department of Clinical Microbiology, School of Medicine, University of Crete, 70013 Heraklion, Greece.
Cancers (Basel). 2024 May 18;16(10):1923. doi: 10.3390/cancers16101923.
Colorectal cancer (CRC) significantly contributes to cancer-related mortality, necessitating the exploration of prognostic factors beyond TNM staging. This study investigates the composition of the gut microbiome and microbial DNA fragments in stage II/III CRC.
A cohort of 142 patients with stage II/III CRC and 91 healthy controls underwent comprehensive microbiome analysis. Fecal samples were collected for rRNA sequencing, and blood samples were tested for the presence of microbial DNA fragments. De novo clustering analysis categorized individuals based on their microbial profiles. Alpha and beta diversity metrics were calculated, and taxonomic profiling was conducted.
Patients with CRC exhibited distinct microbial composition compared to controls. Beta diversity analysis confirmed CRC-specific microbial profiles. Taxonomic profiling revealed unique taxonomies in the patient cohort. De novo clustering separated individuals into distinct groups, with specific microbial DNA fragment detection associated with certain patient clusters.
The gut microbiota can differentiate patients with CRC from healthy individuals. Detecting microbial DNA fragments in the bloodstream may be linked to CRC prognosis. These findings suggest that the gut microbiome could serve as a prognostic factor in stage II/III CRC. Identifying specific microbial markers associated with CRC prognosis has potential clinical implications, including personalized treatment strategies and reduced healthcare costs. Further research is needed to validate these findings and uncover underlying mechanisms.
结直肠癌(CRC)对癌症相关死亡率有显著影响,因此有必要探索TNM分期以外的预后因素。本研究调查II/III期结直肠癌患者肠道微生物群和微生物DNA片段的组成。
对142例II/III期结直肠癌患者和91例健康对照者进行了全面的微生物群分析。采集粪便样本进行rRNA测序,并检测血液样本中微生物DNA片段的存在情况。从头聚类分析根据个体的微生物谱对其进行分类。计算了α和β多样性指标,并进行了分类学分析。
与对照组相比,结直肠癌患者表现出明显不同的微生物组成。β多样性分析证实了结直肠癌特异性微生物谱。分类学分析揭示了患者队列中的独特分类群。从头聚类将个体分为不同的组,特定微生物DNA片段的检测与某些患者簇相关。
肠道微生物群可将结直肠癌患者与健康个体区分开来。检测血液中的微生物DNA片段可能与结直肠癌预后相关。这些发现表明,肠道微生物群可作为II/III期结直肠癌的预后因素。识别与结直肠癌预后相关的特定微生物标志物具有潜在的临床意义,包括个性化治疗策略和降低医疗成本。需要进一步研究来验证这些发现并揭示潜在机制。