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本文引用的文献

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Role of intestinal flora in colorectal cancer from the metabolite perspective: a systematic review.从代谢物角度看肠道菌群在结直肠癌中的作用:一项系统综述
Cancer Manag Res. 2018 Jan 31;10:199-206. doi: 10.2147/CMAR.S153482. eCollection 2018.
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Diet and microbiota linked in health and disease.饮食与微生物组在健康和疾病中相互关联。
Food Funct. 2018 Feb 21;9(2):688-704. doi: 10.1039/c7fo01820g.
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Diabetic cognitive dysfunction is associated with increased bile acids in liver and activation of bile acid signaling in intestine.糖尿病认知功能障碍与肝脏中胆汁酸增加及肠道中胆汁酸信号激活有关。
Toxicol Lett. 2018 May 1;287:10-22. doi: 10.1016/j.toxlet.2018.01.006. Epub 2018 Jan 31.
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Innate and adaptive lymphocytes sequentially shape the gut microbiota and lipid metabolism.先天和适应性淋巴细胞依次塑造肠道微生物群和脂质代谢。
Nature. 2018 Feb 8;554(7691):255-259. doi: 10.1038/nature25437. Epub 2018 Jan 22.
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An in-depth prognostic analysis of baseline blood lipids in predicting postoperative colorectal cancer mortality: The FIESTA study.基线血脂对预测结直肠癌术后死亡率的深入预后分析:FIESTA研究
Cancer Epidemiol. 2018 Feb;52:148-157. doi: 10.1016/j.canep.2018.01.001. Epub 2018 Jan 8.
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Chronic glucocorticoid treatment induced circadian clock disorder leads to lipid metabolism and gut microbiota alterations in rats.慢性糖皮质激素治疗诱导的昼夜节律紊乱导致大鼠脂质代谢和肠道微生物群改变。
Life Sci. 2018 Jan 1;192:173-182. doi: 10.1016/j.lfs.2017.11.049. Epub 2017 Dec 1.
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The fasting serum triglyceride levels of elderly population with different progression stages of diabetes mellitus in China.中国不同糖尿病进展阶段老年人群的空腹血清甘油三酯水平。
J Diabetes Complications. 2017 Dec;31(12):1641-1647. doi: 10.1016/j.jdiacomp.2017.08.011. Epub 2017 Aug 26.
8
Precision Nutrition for Targeting Lipid Metabolism in Colorectal Cancer.精准营养靶向结直肠癌的脂质代谢
Nutrients. 2017 Sep 28;9(10):1076. doi: 10.3390/nu9101076.
9
Probiotic supplementation in diabetic hemodialysis patients has beneficial metabolic effects.益生菌补充剂对糖尿病血液透析患者有有益的代谢作用。
Kidney Int. 2017 Feb;91(2):435-442. doi: 10.1016/j.kint.2016.09.040. Epub 2016 Dec 4.
10
DNA from fecal immunochemical test can replace stool for detection of colonic lesions using a microbiota-based model.粪便免疫化学检测的 DNA 可以替代粪便,用于基于微生物组的模型检测结肠病变。
Microbiome. 2016 Nov 14;4(1):59. doi: 10.1186/s40168-016-0205-y.

参与结直肠癌伴血脂异常的肠道微生物。

Intestinal microorganisms involved in colorectal cancer complicated with dyslipidosis.

机构信息

a Department of Medical Oncology , Huzhou Central Hospital , Huzhou , Zhejiang , China.

b Department of Intervention and Radiotherapy , Huzhou Central Hospital , Huzhou , Zhejiang Province , China.

出版信息

Cancer Biol Ther. 2019;20(1):81-89. doi: 10.1080/15384047.2018.1507255. Epub 2018 Sep 21.

DOI:10.1080/15384047.2018.1507255
PMID:30239257
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6343685/
Abstract

BACKGROUND

Abnormal lipid metabolism is considered to be one of main promoters of colorectal cancer (CRC), and intestinal microorganisms may be involved in CRC in patients with abnormal lipid metabolism.

OBJECTIVE

To investigate lipid metabolism in CRC patients and explore the role of intestinal microorganisms in CRC complicated with abnormal lipid metabolism.

METHODS

Overall, 150 CRC patients in Huzhou Central Hospital from January 2016 to September 2017 were recruited in the present study. Basic patient information and clinical serological indicators were investigated and analyzed. Twenty-one stool samples were collected from patients after receiving informed consent. Next-generation sequencing technology was used to sequence bacterial 16S ribosomal RNA. Bioinformatics analysis was used to profile the microbial composition and screen distinctive bacteria in patients with CRC complicated with abnormal lipid metabolism.

RESULTS

Apo B and FFA levels were higher in patients with stage I disease than in patients with other stages. HDL, LDL, Apo B and FFA levels were higher in female patients than in male patients. FFA level was higher in rectal cancer patients than in colon cancer patients. These differences were statistically significant (p < 0.05). The proportion of Escherichia/Shigella was increased in CRC patients with hyperlipoidaemia and hypercholesteremia; the abundance of Streptococcus was increased in CRC patients with hyperlipoidaemia; the abundance of Clostridium XIVa was reduced in CRC patients with hyperlipoidaemia and hypercholesteremia; and the abundance of Ruminococcaceae was reduced in CRC patients with hypercholesteremia. Bilophila and Butyricicoccus were closely related to CRC patients without hyperlipoidaemia or hypercholesteremia, and Selenomonas, Clostridium, Bacteroidetes Slackia, Burkholderiales and Veillonellaceae were closely related to CRC patients with hyperlipoidaemia. Some pathways, including secretion system, chaperones and folding catalysts, amino sugar and nucleotide sugar metabolism, arginine and proline metabolism, glycine, serine and threonine metabolism, histidine metabolism, pores and ion channels, nitrogen metabolism and sporulation, may be involved in lipid metabolism abnormality in CRC patients.

CONCLUSIONS

Many CRC patients have abnormal lipid metabolism, and the intestinal microbiota is altered in these CRC patients.

摘要

背景

异常的脂质代谢被认为是促进结直肠癌(CRC)的主要因素之一,而肠道微生物可能参与了脂质代谢异常的 CRC 患者的发病过程。

目的

探讨 CRC 患者的脂质代谢情况,并探索肠道微生物在伴有脂质代谢异常的 CRC 中的作用。

方法

本研究共纳入 2016 年 1 月至 2017 年 9 月在湖州市中心医院就诊的 150 例 CRC 患者。调查并分析了患者的基本信息和临床血清学指标。采集 21 例患者知情同意后的粪便样本,采用下一代测序技术对细菌 16S 核糖体 RNA 进行测序。生物信息学分析用于分析微生物组成,并筛选伴有脂质代谢异常的 CRC 患者中具有特征性的细菌。

结果

Ⅰ期患者的载脂蛋白 B(Apo B)和游离脂肪酸(FFA)水平高于其他分期患者。女性患者的高密度脂蛋白(HDL)、低密度脂蛋白(LDL)、Apo B 和 FFA 水平高于男性患者。直肠癌患者的 FFA 水平高于结肠癌患者。这些差异均有统计学意义(P<0.05)。高脂血症和高胆固醇血症患者的大肠杆菌/志贺菌属比例增加;高脂血症患者的链球菌属丰度增加;高脂血症和高胆固醇血症患者的梭菌属 XIVa 减少;高胆固醇血症患者的瘤胃菌科减少。无高脂血症或高胆固醇血症的 CRC 患者与Bilophila 和 Butyricicoccus 密切相关,无高脂血症或高胆固醇血症的 CRC 患者与 Selenomonas、Clostridium、拟杆菌属 Slackia、伯克霍尔德菌目和韦荣球菌科密切相关。一些途径,包括分泌系统、伴侣和折叠催化剂、氨基酸糖和核苷酸糖代谢、精氨酸和脯氨酸代谢、甘氨酸、丝氨酸和苏氨酸代谢、组氨酸代谢、孔和离子通道、氮代谢和孢子形成,可能与 CRC 患者的脂质代谢异常有关。

结论

许多 CRC 患者存在异常的脂质代谢,且这些 CRC 患者的肠道微生物发生改变。