植物乳杆菌和细菌肽聚糖对小鼠体内外肿瘤生长的影响

Arpa Aintablian, D. F. Jaber, M. Jallad, A. Abdelnoor
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引用次数: 4

摘要

微生物群的一些成员已被证明是通过刺激宿主抗肿瘤免疫反应来抑制肿瘤生长的有效策略。当肠道微生物群成员植物乳杆菌(Lp)用于治疗小鼠的结直肠癌癌症时,观察到了抗肿瘤免疫效果。此外,包括肽聚糖(PG)在内的细菌成分已被证明具有抑瘤作用。本研究的目的是在体内研究Lp对荷黑色素瘤小鼠血清血管生成和免疫刺激细胞因子水平的抗肿瘤作用;以及PG在体外对小鼠黑色素瘤和乳腺癌症细胞生长的影响。将50只C57BL/6雌性小鼠分为两组。在肿瘤植入之前,实验组经口灌胃给予Lp 2周。在接受B16F10黑色素瘤细胞的皮下注射后,实验组继续每周一次Lp给药,持续3周。最后一次细菌给药后,通过ELISA测定血清血管内皮生长因子(VEGF)和白细胞介素-12(IL-12)的水平。此外,对两组小鼠的存活情况进行监测。此外,将B16F10黑色素瘤和EMT6乳腺癌症细胞分别与两种PG浓度孵育48小时,并测定生存率百分比。在用Lp治疗的组中观察到血清VEGF水平的显著降低和血清IL-12水平的显著升高。此外,在体外用Lp处理的组中注意到20%的存活率,在用PG孵育48小时后观察到小鼠黑色素瘤和癌症细胞的生存力的显著降低。看来Lp具有抗肿瘤活性,通过刺激免疫系统和抑制血管生成。此外,Lp似乎通过PG具有直接的肿瘤抑制作用。
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The Effect of Lactobacillus Plantarum and Bacterial Peptidoglycan on the Growth of Mouse Tumors in vivo and in vitro
Some members of the microbiota have been shown to be effective strategies for inhibiting tumor growth through stimulation of host anti-tumor immune responses. Anti-tumor immune effects were observed when Lactobacillus plantarum (Lp), a member of the gut microbiota, was used to treat colorectal cancer in mice. Moreover, constituents of bacteria, including peptidoglycan (PG), have been shown to exhibit tumoricidal effects. The aim of this study was to investigate the anti-tumor effects of Lp on serum levels of angiogenic and immunostimulatory cytokines in melanoma-bearing mice in vivo; as well as the effect of PG on the growth of mouse melanoma and breast cancer cells in vitro.  Fifty C57BL/6 female mice were divided into two groups. Prior to tumor implantation, Lp was administered via oral gavage for 2 weeks to the experimental group. After receiving subcutaneous injections of B16F10 melanoma cells, Lp administration was continued once per week for 3 weeks to the experimental group. After the last bacterial administration, serum levels of Vascular Endothelial Growth Factor (VEGF) and Interleukin-12 (IL-12) were determined by ELISA. Additionally, mice from both groups were monitored for survival. Moreover, B16F10 melanoma and EMT6 breast cancer cells were incubated separately with two PG concentrations for 48 h and percent viability was determined. A significant decrease in the serum levels of VEGF and a significant increase in the serum levels of IL-12 were observed in the group treated with Lp Moreover, 20% survival rate was noted in the group treated with Lp in vitro, a marked decrease in the viability of mouse melanoma and breast cancer cells was observed 48 h post-incubation with PG. It appears that Lp possesses anti-tumor activity, by both stimulating the immune system and suppressing angiogenesis. Moreover, Lp appears to have a direct tumoricidal effect through PG.
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