Zhou Ping, Zhang Wangzheqi, Liao Yan, Zhai Zhiyong, Lu Sicun, Jiang Shuya, Hu Wei, Gong Wei
Department of Gastroenterology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Faculty of Anesthesiology, Changhai Hospital, Naval Medical University, Shanghai, 200433 China.
Int J Surg. 2025 May 30. doi: 10.1097/JS9.0000000000002573.
Colorectal cancer (CRC) is one of the most prevalent cancers worldwide and poses significant clinical challenges. In the context of multi-omics advancements, the intricate relationships between the gut microbiota and the onset, progression, and treatment responses of CRC, as well as the components of the suppressive tumour immune microenvironment (TME), have become increasingly evident. Researchers have found that pathogenic bacteria in the gut release metabolites and proteins that affect the development of CRC by interfering with the host's colonic epithelium and immune system. The gut microbiota has been implicated in modulating responses to chemotherapy, targeted therapy, and immunotherapy in CRC patients. Ongoing research is focused on combination therapies designed to achieve optimal efficacy by activating anti-tumour immune cells within the TME. In this review, we summarise the current understanding of the role of the gut microbiota in CRC, focus on how the gut microbiota influences the TME, explore the development prospects of the gut microbiota and TME as potential biomarkers, and discuss the translational and clinical implications of microbiota-related treatments in combination with immunotherapy and other therapeutic approaches for the precise prevention and treatment of CRC.
The interactions between the immune microenvironment and the gut microbiota during the development and treatment of colorectal cancer (CRC) are still under exploration. In this review, we focus on CRC and the gut microbiota, which can modulate the tumor immune microenvironment (TME) of CRC. As such, both the gut microbiota and the TME have the potential to serve as biomarkers. Furthermore, we emphasize the prospective applications of microbiota-modifying therapies, when combined with immunotherapy and molecular targeted therapies, for the precise treatment of CRC.
结直肠癌(CRC)是全球最常见的癌症之一,带来了重大的临床挑战。在多组学进展的背景下,肠道微生物群与CRC的发生、发展及治疗反应之间的复杂关系,以及抑制性肿瘤免疫微环境(TME)的组成部分,已变得越来越明显。研究人员发现,肠道中的病原菌释放代谢产物和蛋白质,通过干扰宿主的结肠上皮和免疫系统来影响CRC的发展。肠道微生物群与CRC患者对化疗、靶向治疗和免疫治疗的反应调节有关。正在进行的研究集中在通过激活TME内的抗肿瘤免疫细胞来实现最佳疗效的联合治疗。在本综述中,我们总结了目前对肠道微生物群在CRC中作用的理解,重点关注肠道微生物群如何影响TME,探讨肠道微生物群和TME作为潜在生物标志物的发展前景,并讨论微生物群相关治疗与免疫治疗及其他治疗方法联合用于CRC精准预防和治疗的转化及临床意义。
在结直肠癌(CRC)的发生和治疗过程中,免疫微环境与肠道微生物群之间的相互作用仍在探索中。在本综述中,我们关注CRC和肠道微生物群,其可调节CRC的肿瘤免疫微环境(TME)。因此,肠道微生物群和TME都有潜力作为生物标志物。此外,我们强调了微生物群调节疗法与免疫疗法和分子靶向疗法联合用于CRC精准治疗的前瞻性应用。