Sudaarsan Aruna Senthil Kumar, Ghosh Asit Ranjan
Department of Integrative Biology, School of Bio Sciences and Technology (SBST), Vellore Institute of Technology (VIT), Vellore, Tamil Nadu, India.
Front Pharmacol. 2024 Sep 20;15:1436021. doi: 10.3389/fphar.2024.1436021. eCollection 2024.
Cancer remains a multifactorial disease with an increased mortality rate around the world for the past several decades. Despite advancements in treatment strategies, lower survival rates, drug-associated side effects, and drug resistance create a need for novel anticancer agents. Ample evidence shows that imbalances in the gut microbiota are associated with the formation of cancer and its progression. Altering the gut microbiota via probiotics and their metabolites has gained attention among the research community as an alternative therapy to treat cancer. Probiotics exhibit health benefits as well as modulate the immunological and cellular responses in the host. Apart from probiotics, their secreted products like bacteriocins, exopolysaccharides, short-chain fatty acids, conjugated linoleic acid, peptidoglycan, and other metabolites are found to possess anticancer activity. The beneficiary role of these postbiotic compounds is widely studied for characterizing their mechanism and mode of action that reduces cancer growth. The present review mainly focuses on the postbiotic components that are employed against cancer with their reported mechanism of action. It also describes recent research works carried out so far with specific strain and anticancer activity of derived compounds both and , validating that the probiotic approach would pave an alternative way to reduce the burden of cancer.
在过去几十年里,癌症仍然是一种多因素疾病,全球死亡率不断上升。尽管治疗策略有所进步,但较低的生存率、药物相关的副作用和耐药性使得人们需要新型抗癌药物。大量证据表明,肠道微生物群的失衡与癌症的形成及其进展有关。通过益生菌及其代谢产物改变肠道微生物群作为一种治疗癌症的替代疗法,已引起研究界的关注。益生菌不仅具有健康益处,还能调节宿主的免疫和细胞反应。除了益生菌,它们分泌的产物如细菌素、胞外多糖、短链脂肪酸、共轭亚油酸、肽聚糖和其他代谢产物也被发现具有抗癌活性。这些后生元化合物的有益作用已被广泛研究,以确定其减少癌症生长的机制和作用方式。本综述主要关注用于抗癌的后生元成分及其报道的作用机制。它还描述了迄今为止针对特定菌株及其衍生化合物的抗癌活性所开展的最新研究工作,证实益生菌方法将为减轻癌症负担开辟一条替代途径。