Cellular and Molecular Medicine Department, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Department of Pathology, University of Montreal, Montreal, Quebec, Canada.
Cancer Med. 2024 Oct;13(19):e70277. doi: 10.1002/cam4.70277.
Immune stressors, such as lipopolysaccharides (LPS), profoundly affect microbiota balance, leading to gut dysbiosis. This imbalance disrupts the metabolic phenotype and structural integrity of the gut, increasing intestinal permeability. During puberty, a critical surge in estrogen levels is crucial for mammary gland development. However, inflammation originating from the gut in this period may interfere with this development, potentially heightening breast cancer risk later. The long-term effects of pubertal inflammation on mammary development and breast cancer risk are underexplored. Such episodes can dysregulate cytokine levels and microRNA expression, altering mammary cell gene expression, and predisposing them to tumorigenesis.
This study hypothesizes that prebiotics, specifically Lentinula edodes Cultured Extract (AHCC), can counteract LPS's adverse effects. Using BALB/c mice, an acute LPS dose was administered at puberty, and breast cancer predisposition was assessed at 13 weeks. Cytokine and tumor-related microRNA levels, tumor development, and cancer stem cells were explored through immunoassays and qRT-PCR.
Results show that LPS induces lasting effects on cytokine and microRNA expression in mammary glands and tumors. AHCC modulates cytokine expression, including IL-1β, IL-17A/F, and IL-23, and mitigates LPS-induced IL-6 in mammary glands. It also regulates microRNA expression linked to tumor progression and suppression, particularly counteracting the upregulation of oncogenic miR-21, miR-92, and miR-155. Although AHCC slightly alters some tumor-suppressive microRNAs, these changes are modest, highlighting a complex regulatory role that warrants further study.
These findings underscore the potential of dietary interventions like AHCC to mitigate pubertal LPS-induced inflammation on mammary gland development and tumor formation, suggesting a preventive strategy against breast cancer.
免疫应激原,如脂多糖(LPS),会深刻影响微生物群平衡,导致肠道菌群失调。这种失衡会破坏肠道的代谢表型和结构完整性,增加肠道通透性。在青春期,雌激素水平的急剧上升对乳腺发育至关重要。然而,这个时期来自肠道的炎症可能会干扰这种发育,从而增加日后患乳腺癌的风险。青春期炎症对乳腺发育和乳腺癌风险的长期影响尚未得到充分探索。这种炎症会使细胞因子水平和 microRNA 表达失调,改变乳腺细胞的基因表达,使它们容易发生肿瘤发生。
本研究假设,益生菌,特别是香菇菌丝体培养提取物(AHCC)可以抵消 LPS 的不良影响。使用 BALB/c 小鼠,在青春期给予急性 LPS 剂量,并在 13 周时评估乳腺癌易感性。通过免疫测定和 qRT-PCR 研究细胞因子和与肿瘤相关的 microRNA 水平、肿瘤发展和癌症干细胞。
结果表明,LPS 对乳腺和肿瘤中的细胞因子和 microRNA 表达产生持久影响。AHCC 调节细胞因子表达,包括 IL-1β、IL-17A/F 和 IL-23,并减轻 LPS 在乳腺中的 IL-6 表达。它还调节与肿瘤进展和抑制相关的 microRNA 表达,特别是对抗致癌 miR-21、miR-92 和 miR-155 的上调。尽管 AHCC 略微改变了一些肿瘤抑制 microRNAs,但这些变化是适度的,强调了其复杂的调节作用,需要进一步研究。
这些发现强调了膳食干预(如 AHCC)的潜力,可以减轻青春期 LPS 诱导的炎症对乳腺发育和肿瘤形成的影响,为预防乳腺癌提供了一种策略。