Pezeshki Babak, Abdulabbas Hussein T, Alturki Ahmed D, Mansouri Pegah, Zarenezhad Elham, Nasiri-Ghiri Mahdi, Ghasemian Abdolmajid
Noncommunicable Diseases Research Center, Fasa University of Medical Sciences, Fasa, Iran.
Department of Medical Microbiology, Medical College, Al Muthanna University, Samawah, Al Muthanna, Iraq.
Probiotics Antimicrob Proteins. 2025 Jan 28. doi: 10.1007/s12602-025-10462-0.
Research into the role of probiotics-often referred to as "living supplements"-in cancer therapy is still in its early stages, and uncertainties regarding their effectiveness remain. Relevantly, chemopreventive and therapeutic effects of probiotics have been determined. There is also substantial evidence supporting their potential in cancer treatment such as immunotherapy. Probiotics employ various mechanisms to inhibit cancer initiation and progression. These include colonizing and protecting the gastrointestinal tract (GIT), producing metabolites, inducing apoptosis and autophagy, exerting anti-inflammatory properties, preventing metastasis, enhancing the effectiveness of immune checkpoint inhibitors (ICIs), promoting cancer-specific T cell infiltration, arresting the cell cycle, and exhibiting direct or indirect synergistic effects with anticancer drugs. Additionally, probiotics have been shown to activate tumor suppressor genes and inhibit pro-inflammatory transcription factors. They also increase reactive oxygen species production within cancer cells. Synergistic interactions between probiotics and various anticancer drugs, such as cisplatin, cyclophosphamide, 5-fluorouracil, trastuzumab, nivolumab, ipilimumab, apatinib, gemcitabine, tamoxifen, sorafenib, celecoxib and irinotecan have been observed. The combination of probiotics with anticancer drugs holds promise in overcoming drug resistance, reducing recurrence, minimizing side effects, and lowering treatment costs. In addition, fecal microbiota transplantation (FMT) and prebiotics supplementation has increased cytotoxic T cells within tumors. However, probiotics may leave some adverse effects such as risk of infection and gastrointestinal effects, antagonistic effects with drugs, and different responses among patients. These findings highlight insights for considering specific strains and engineered probiotic applications, preferred doses and timing of treatment, and personalized therapies to enhance the efficacy of cancer therapy. Accordingly, targeted interventions and guidelines establishment needs extensive randomized controlled trials as probiotic-based cancer therapy has not been approved by Food and Drug Administration (FDA).
对益生菌(通常被称为“活性补充剂”)在癌症治疗中作用的研究仍处于早期阶段,其有效性仍存在不确定性。相关地,益生菌的化学预防和治疗作用已得到确定。也有大量证据支持它们在癌症治疗如免疫疗法中的潜力。益生菌通过多种机制抑制癌症的发生和发展。这些机制包括定殖和保护胃肠道、产生代谢产物、诱导细胞凋亡和自噬、发挥抗炎特性、防止转移、增强免疫检查点抑制剂(ICI)的有效性、促进癌症特异性T细胞浸润、使细胞周期停滞,以及与抗癌药物表现出直接或间接的协同作用。此外,益生菌已被证明可激活肿瘤抑制基因并抑制促炎转录因子。它们还会增加癌细胞内活性氧的产生。已观察到益生菌与多种抗癌药物之间的协同相互作用,如顺铂、环磷酰胺、5-氟尿嘧啶、曲妥珠单抗、纳武单抗、伊匹单抗、阿帕替尼、吉西他滨、他莫昔芬、索拉非尼、塞来昔布和伊立替康。益生菌与抗癌药物联合使用有望克服耐药性、减少复发、将副作用降至最低并降低治疗成本。此外,粪便微生物群移植(FMT)和补充益生元增加了肿瘤内的细胞毒性T细胞。然而,益生菌可能会产生一些不良影响,如感染风险和胃肠道影响、与药物的拮抗作用以及患者之间的不同反应。这些发现为考虑特定菌株和工程益生菌的应用、优选的剂量和治疗时机以及个性化疗法以提高癌症治疗效果提供了见解。因此,由于基于益生菌的癌症治疗尚未获得美国食品药品监督管理局(FDA)的批准,针对性干预措施和指南的制定需要广泛的随机对照试验。