Zuraik Abdulrahman A, Daboul Yaman, Awama M Ayman, Yazigi Haitham, Kayasseh Moh'd Azzam, Georges Michael
Department of Biochemistry and Microbiology, Faculty of Pharmacy, Tishreen University, Lattakia, Syria.
School of Biological Sciences, Queens University Belfast, Belfast, UK.
Indian J Microbiol. 2024 Dec;64(4):1938-1950. doi: 10.1007/s12088-024-01279-6. Epub 2024 Apr 22.
An intricate relationship exists, and interactions occur between the gut microbiota and colorectal cancer (CRC). Recent studies have indicated that inflammatory reactions stimulated by () lead to the development of CRC. Radical surgery combined with adjuvant chemotherapy is the primary treatment approach for most CRC patients. This study was designed to evaluate the abundance of as part of the gut microbiota in patients with CRC compared to healthy individuals and to assess the effect of the gut microbiota on patients undergoing adjuvant chemotherapy and those experiencing CRC relapse. There were 201 participants, comprising 50 healthy controls and 151 CRC patients. Stool samples were collected from three CRC groups (postoperatively, chemotherapy and relapse), and the fourth was the healthy control group. The amount of in each sample was analyzed using quantitative loop-mediated isothermal amplification-phenol red (QLAMP-PhR), a novel biomolecular method that targets regions encoding the specific gene. Compared with healthy control stool samples, the levels were significantly elevated in all CRC patient groups ( < 0.001), and it was significantly more frequent in the CRC relapse patients (group C) ( < 0.001). In addition, abundance increased significantly in the distal colon compared to the proximal colon ( < 0.001). Both CRC relapse and chemotherapy exert significant reciprocal effects on the gut microbiota of CRC patients. Microbiota-based intervention may be beneficial for patients during postoperative care, especially in CRC relapsing cases. : This study of the clinical trial has been registered in the ISRCTN registry with study registration number ISRCTN53358464. https://www.isrctn.com/ISRCTN53358464.
The online version contains supplementary material available at 10.1007/s12088-024-01279-6.
肠道微生物群与结直肠癌(CRC)之间存在复杂的关系和相互作用。最近的研究表明,由()刺激的炎症反应会导致CRC的发展。根治性手术联合辅助化疗是大多数CRC患者的主要治疗方法。本研究旨在评估CRC患者与健康个体相比,作为肠道微生物群一部分的()丰度,并评估肠道微生物群对接受辅助化疗的患者和经历CRC复发的患者的影响。共有201名参与者,包括50名健康对照者和151名CRC患者。从三个CRC组(术后、化疗和复发)收集粪便样本,第四组为健康对照组。使用定量环介导等温扩增-酚红(QLAMP-PhR)分析每个样本中()的含量,QLAMP-PhR是一种针对编码特定()基因区域的新型生物分子方法。与健康对照粪便样本相比,所有CRC患者组中的()水平均显著升高(<0.001),并且在CRC复发患者(C组)中更为频繁(<0.001)。此外,与近端结肠相比,远端结肠中的()丰度显著增加(<0.001)。CRC复发和化疗对CRC患者的肠道微生物群()均产生显著的相互影响。基于微生物群的干预可能对患者术后护理有益,尤其是在CRC复发病例中。:本临床试验研究已在ISRCTN注册中心注册,研究注册号为ISRCTN53358464。https://www.isrctn.com/ISRCTN53358464。
在线版本包含可在10.1007/s12088-024-01279-6获取的补充材料。