摘要:薄茅水提物通过改变小鼠肠道菌群来抑制肺癌的生长

D. Upreti, Susumu Ishiguro, Mayme Loyd, Nicole Robben, P. Cote, Morgan Phillips, Ayaka Nakashima, Kengo Suzuki, J. Comer, M. Tamura
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引用次数: 0

摘要

细叶藻是一种单细胞藻类,富含营养,因此被用作营养膳食补充剂。这种藻类可以在淡水和咸水中找到,具有植物和动物的双重特征。薄叶草提取物具有广泛的药用特性,包括刺激抗癌免疫,对抗多种类型的癌症;然而,其抗癌机制尚未完全阐明。因此,研究了一种不含水不溶性成熟副滑膜的薄叶菊水提取物作为肺癌的抗癌剂。以整株秋葵的干粉为原料,制备了两种不同的提取物。首先,将干粉悬浮在PBS中,10000 g离心20 min,然后用孔径0.22µm的膜过滤,制备部分纯化水提物(EWE)。其次,将未过滤的羊皮纸浸泡在沸水中12 min, 10000 g离心10 min,用孔径为0.22µm的膜过滤,制备煮沸羊皮纸(bEWE)。EWE和bEWE处理均能抑制体外肺癌细胞的生长,且呈剂量和时间依赖性。两种提取物均能显著抑制Lewis肺癌(LLC)细胞的三维生长。流式细胞术分析显示,EWE处理能减弱骨髓细胞培养中的粒细胞髓源性抑制细胞(MDSCs)。体内研究采用小鼠LLC原位同种异体移植模型进行。在LLC细胞接种前3周口服EWE和bEWE (100-200 mg/kg/天)可减弱免疫功能小鼠肺部肿瘤的生长,同时减少外周粒细胞。然而,在LLC细胞接种后开始的提取物处理中没有看到这种衰减。bEWE治疗比EWE治疗更有效地抑制肿瘤生长。通过16s rRNA基因扩增子测序分析小鼠粪便微生物组,结果显示三组(EWE, bEWE和PBS对照)的α多样性相似,但EWE和bEWE处理小鼠的微生物组成比PBS组更多样化。具体来说,观察到拟杆菌门与厚壁菌门的比例增加,并且在EWE和bEWE处理的小鼠中检测到Akkermansia和Muribaculum显著增加。这些研究表明,口服部分纯化的薄叶草水提取物可以改变肠道微生物群,这种改变可能会减弱宿主的MDSCs,从而阻止肺癌的生长。本研究得到2016EUGLENA-RC1 (MT), 2017EUGLENA-RC2 (MT and JC),堪萨斯州立大学兽医学院SMILE奖(MT and JC)和NIH资助P20 RR017686 (MT)的支持。引文格式:Deepa Upreti, Susumu Ishiguro, Mayme lloyd, Nicole Robben, Paige Cote, Morgan Phillips, Ayaka Nakashima, Kengo Suzuki, Jeffrey Comer, Masaaki Tamura。薄叶草水提物通过改变小鼠肠道菌群来抑制肺癌的生长[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):2588。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract 2588: Oral administration of water extract fromEuglena gracilisprevents lung carcinoma growth in mice by alteration of intestinal microbiota
Euglena gracilis, a single-celled alga, is rich in nutrients and thus, used as a nutritional dietary supplement. This alga can be found in both fresh and saltwater and possesses characteristics of both plants and animals. Euglena gracilis extracts have a wide range of medicinal properties including stimulation of anticancer immunity against multiple types of cancers; however, the anticancer mechanism has not yet been fully elucidated. Therefore, a water extract from Euglena gracilis devoid of water-insoluble mature paramylons was evaluated as an anticancer agent against lung carcinoma. Two different extracts were prepared using dried powder from whole Euglena gracilis. First, partially purified water extract (EWE) was prepared by suspending dry powder in PBS and centrifugation at 10,000g for 20 min followed by a filtration using a 0.22µm pore size membrane. Second, boiled EWE (bEWE) was prepared by immersing unfiltered EWE in boiling water for 12 min followed by centrifugation at 10,000g for 10 min and filtration using 0.22µm pore size membrane. Both EWE and bEWE treatments inhibited the growth of lung carcinoma cells in vitro in a dose- and time-dependent manner. Furthermore, both extracts significantly inhibited the three-dimensional growth of Lewis Lung Carcinoma (LLC) cells. Flow cytometry analysis showed that the EWE treatment attenuates granulocytic myeloid-derived suppressor cells (MDSCs) in bone marrow cell cultures. The in vivo study was conducted using a mouse LLC orthotopic allograft model. Oral administration of EWE and bEWE (100-200 mg/kg/day) three weeks prior to LLC cell inoculation attenuated the tumor growth in the lungs of immunocompetent mice while decreasing the peripheral granulocytes. However, this attenuation was not seen for the extract treatment initiated after LLC cell inoculation. The tumor growth attenuation was more efficient with the bEWE treatment than with EWE treatment. The fecal microbiomes of the mice were analyzed by 16s rRNA gene amplicon sequencing which revealed that alpha diversity in three groups (EWE, bEWE, and PBS control) was similar, however, the microbial compositions of the EWE- and bEWE-treated mouse groups were more diversified than in the PBS group. Specifically, an increase in the ratio of Bacteroidetes to Firmicutes was observed, and a significant increase in Akkermansia and Muribaculum was detected in EWE- and bEWE- treated mice compared to PBS treated mice. These studies suggest that oral administration of partially purified water extracts from Euglena gracilis altered the intestinal microbiome and the alteration may attenuate host MDSCs, thereby preventing lung carcinoma growth. This study was supported by 2016EUGLENA-RC1 (MT), 2017EUGLENA-RC2 (MT and JC), Kansas State University College of Veterinary Medicine SMILE award (MT and JC), and NIH grant P20 RR017686 (MT). Citation Format: Deepa Upreti, Susumu Ishiguro, Mayme Loyd, Nicole Robben, Paige Cote, Morgan Phillips, Ayaka Nakashima, Kengo Suzuki, Jeffrey Comer, Masaaki Tamura. Oral administration of water extract from Euglena gracilis prevents lung carcinoma growth in mice by alteration of intestinal microbiota [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2588.
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