Paraskevaidis Ioannis, Tsougos Elias, Kourek Christos
Medical School of Athens, National and Kapodistrian University of Athens, 15772 Athens, Greece.
Department of Cardiology, Hygeia Hospital, 15123 Athens, Greece.
Biomedicines. 2025 May 25;13(6):1297. doi: 10.3390/biomedicines13061297.
In humans, heart failure (HF) and cancer are among the leading causes of morbidity and mortality. A growing body of evidence highlights a bidirectional relationship between these conditions, underpinned by shared risk factors and overlapping pathophysiological pathways. This review aims to explore the emerging role of the intestinal microbiome as a common mechanistic link between HF and cancer. Specifically, we examine how microbial dysbiosis and its metabolic products-such as trimethylamine N-oxide (TMAO), short-chain fatty acids (SCFAs), bile acids, lipopolysaccharides (LPS), and branched-chain amino acids (BCAAs)-contribute to inflammation, immune dysregulation, oxidative stress, and metabolic dysfunction. These mechanisms promote multiorgan impairment and establish a vicious cycle that fuels both tumorigenesis and cardiac deterioration. HF, cancer, and the gut microbiome are not isolated entities but are deeply interconnected through shared biological mechanisms-including chronic inflammation, microbial dysbiosis, immune and neurohumoral modulation, and metabolic derangement. These findings support the concept of a microbiome-centered axis involving the gut, heart, and tumors, which may underlie many chronic disease processes. Understanding these interactions may provide novel insights into disease pathogenesis and uncover promising therapeutic targets that leverage microbiome modulation to prevent or treat HF, cancer, and other systemic diseases.
在人类中,心力衰竭(HF)和癌症是发病和死亡的主要原因。越来越多的证据凸显了这些疾病之间的双向关系,其基础是共同的风险因素和重叠的病理生理途径。本综述旨在探讨肠道微生物群作为HF和癌症之间共同机制联系的新作用。具体而言,我们研究了微生物失调及其代谢产物——如氧化三甲胺(TMAO)、短链脂肪酸(SCFAs)、胆汁酸、脂多糖(LPS)和支链氨基酸(BCAAs)——如何导致炎症、免疫失调、氧化应激和代谢功能障碍。这些机制促进多器官损伤并建立一个恶性循环,加剧肿瘤发生和心脏恶化。HF、癌症和肠道微生物群并非孤立的实体,而是通过包括慢性炎症、微生物失调、免疫和神经体液调节以及代谢紊乱在内的共同生物学机制紧密相连。这些发现支持了以微生物群为中心的涉及肠道、心脏和肿瘤的轴的概念,这可能是许多慢性疾病过程的基础。了解这些相互作用可能为疾病发病机制提供新的见解,并揭示有前景的治疗靶点,利用微生物群调节来预防或治疗HF、癌症和其他全身性疾病。