Dysbiosis and extraintestinal cancers.

IF 12.8 1区 医学 Q1 ONCOLOGY Journal of Experimental & Clinical Cancer Research Pub Date : 2025-02-07 DOI:10.1186/s13046-025-03313-x
Ruishan He, Pingqian Qi, Linzhen Shu, Yidan Ding, Peng Zeng, Guosheng Wen, Ying Xiong, Huan Deng
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Abstract

The gut microbiota plays a crucial role in safeguarding host health and driving the progression of intestinal diseases. Despite recent advances in the remarkable correlation between dysbiosis and extraintestinal cancers, the underlying mechanisms are yet to be fully elucidated. Pathogenic microbiota, along with their metabolites, can undermine the integrity of the gut barrier through inflammatory or metabolic pathways, leading to increased permeability and the translocation of pathogens. The dissemination of pathogens through the circulation may contribute to the establishment of an immune-suppressive environment that promotes carcinogenesis in extraintestinal organs either directly or indirectly. The oncogenic cascade always engages in the disruption of hormonal regulation and inflammatory responses, the induction of genomic instability and mutations, and the dysregulation of adult stem cell proliferation. This review aims to comprehensively summarize the existing evidence that points to the potential role of dysbiosis in the malignant transformation of extraintestinal organs such as the liver, breast, lung, and pancreas. Additionally, we delve into the limitations inherent in current methodologies, particularly the challenges associated with differentiating low loads gut-derived microbiome within tumors from potential sample contamination or symbiotic microorganisms. Although still controversial, an understanding of the contribution of translocated intestinal microbiota and their metabolites to the pathological continuum from chronic inflammation to tumors could offer a novel foundation for the development of targeted therapeutics.

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生态失调和肠外癌症。
肠道菌群在保护宿主健康和推动肠道疾病进展方面发挥着至关重要的作用。尽管最近在生态失调和肠外癌症之间的显著相关性方面取得了进展,但其潜在机制尚未得到充分阐明。致病微生物群及其代谢物可通过炎症或代谢途径破坏肠道屏障的完整性,导致通透性增加和病原体易位。病原体通过血液循环的传播可能有助于建立一个免疫抑制环境,直接或间接地促进肠外器官的癌变。致癌级联反应总是参与激素调节和炎症反应的破坏,诱导基因组不稳定和突变,以及成体干细胞增殖的失调。本文旨在全面总结现有证据,指出生态失调在肠外器官(如肝、乳腺、肺和胰腺)恶性转化中的潜在作用。此外,我们深入研究了当前方法固有的局限性,特别是与区分肿瘤内低负荷肠道来源微生物组与潜在样品污染或共生微生物相关的挑战。尽管仍有争议,但了解易位肠道微生物群及其代谢物对从慢性炎症到肿瘤的病理连续体的贡献可以为靶向治疗的发展提供新的基础。
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来源期刊
CiteScore
18.20
自引率
1.80%
发文量
333
审稿时长
1 months
期刊介绍: The Journal of Experimental & Clinical Cancer Research is an esteemed peer-reviewed publication that focuses on cancer research, encompassing everything from fundamental discoveries to practical applications. We welcome submissions that showcase groundbreaking advancements in the field of cancer research, especially those that bridge the gap between laboratory findings and clinical implementation. Our goal is to foster a deeper understanding of cancer, improve prevention and detection strategies, facilitate accurate diagnosis, and enhance treatment options. We are particularly interested in manuscripts that shed light on the mechanisms behind the development and progression of cancer, including metastasis. Additionally, we encourage submissions that explore molecular alterations or biomarkers that can help predict the efficacy of different treatments or identify drug resistance. Translational research related to targeted therapies, personalized medicine, tumor immunotherapy, and innovative approaches applicable to clinical investigations are also of great interest to us. We provide a platform for the dissemination of large-scale molecular characterizations of human tumors and encourage researchers to share their insights, discoveries, and methodologies with the wider scientific community. By publishing high-quality research articles, reviews, and commentaries, the Journal of Experimental & Clinical Cancer Research strives to contribute to the continuous improvement of cancer care and make a meaningful impact on patients' lives.
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