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盆腔恶性肿瘤患者放疗后肠道菌群变化与放射性肠炎的相关性研究
作者:朱小月1  江柯炜2  陈海娇2  朱琳2  张婷2  刘鹏飞2  吴群英2  王坚2  殷华芳2  沈卫东2 
单位:1. 徐州医科大学, 江苏 徐州 221000;
2. 徐州医科大学附属江阴临床学院, 江苏 江阴 214400
关键词:盆腔肿瘤 放射治疗 放射性肠炎 肠道菌群 炎症因子 
分类号:R737.33
出版年·卷·期(页码):2022·41·第三期(364-371)
摘要:

目的:研究盆腔恶性肿瘤患者放疗后肠道菌群变化,并分析其与脂多糖(LPS)、肿瘤坏死子因子-α(TNF-α)、白细胞介素-1β(IL-1β)及高迁移率族蛋白B1(HMGB1)等炎症因子的相关性,探讨其在预测放射性肠炎中的临床价值。方法:选取2020年10月至2021年6月在徐州医科大学附属江阴临床学院收治的17例首次接受盆腔放疗患者,按照RTOG/EORTC放射反应分级标准分为无症状组、轻症组和重症组。采用16S rDNA测序法检测肠道菌群情况,酶联免疫吸附试验检测炎症因子水平,并进行相关性分析。结果:放疗后患者肠道菌群α多样性明显下降,且放疗前后组间β多样性也存在差异(Stress<0.1)。放疗前重症组患者粪便中Castellaniella属显著高于轻症组和无症状组(P<0.05)。随着放疗剂量累计炎症因子水平明显升高,且变化幅度与放射反应严重等级相关。放疗第3周重症组血清LPS、TNF-α、IL-1β及粪便HMGB1水平高于无症状组和轻症组,差异均有统计学意义(P<0.05)。代表肠道菌群丰度Chao1指数与血清LPS、TNF-α及粪便HMGB1呈负相关(r值分别为-0.655、-0.516、-0.623,均P<0.05);代表肠道菌群多样性Shannon指数与血清LPS呈负相关(r=-0.550,P<0.05)。结论:肠道菌群可能在放射性肠炎的发生、发展中起一定作用。通过检测患者肠道菌群Castellaniella可预测放射性肠炎严重程度,从而为预测及防治放射性肠损伤提供新的思路和方法。

Objective: To study the changes of intestinal flora in patients with pelvic malignant tumor during radiotherapy, and analyze its relationship with lipopolysaccharide(LPS), tumor necrosis factor-α(TNF-α), interleukin-1β(IL-1β) and high mobility group protein B1(HMGB1), and to investigate its clinical value in predicting radiation enteritis. Methods: A total of 17 patients who received pelvic radiotherapy for the first time in Jiangyin Clinical College Affiliated to Xuzhou Medical University from October 2020 to June 2021 were selected and divided into asymptomatic group, mild group and severe group according to the standard of RTOG/EORTC. The intestinal flora was detected by DNA sequencing, and the level of serum inflammatory factors was detected by enzyme-linked immunosorbent assay. Results: The alpha diversity of intestinal flora decreased significantly after radiotherapy, and there were also differences in beta diversity between groups before and after radiotherapy(stress<0.1). Before radiotherapy, Castellaniella-genus in feces of the severe group was significantly higher than that of the mild group and the asymptomatic group(P<0.05). With the cumulative radiation dose, the level of inflammatory factors increased significantly, and the range of change was related to the severity of radiation reaction. The levels of serum LPS, TNF-α, IL-1β and fecal HMGB1 in the severe group in the third week of radiotherapy were significantly higher than those in the asymptomatic group and the mild group(P<0.05).The Chao1 index representing the abundance of intestinal flora was negatively correlated with LPS and TNF-α in serum and HMGB1 in feces(r=-0.655, -0.516, -0.623, all P<0.05); Shannon index, representing the diversity of intestinal flora, was negatively correlated with LPS in serum(r=-0.550, P<0.05).Conclusion: Intestinal flora may play a role in the occurrence and development of radiation enteritis. The severity of radiation enteritis can be predicted by detecting the castellaniella genus of intestinal flora, which provides a new idea and method for predicting and preventing radiation intestinal injury.

参考文献:

[1] CHAI Y,WANG J,GAO Y,et al.Identification of biomarkers for radiation-induced acute intestinal symptoms(RIAISs) in cervical cancer patients by serum protein profiling[J].J Radiat Res,2015,56(1):134-140.
[2] 童金龙,田小强,王礼学,等.姑息放疗在治疗晚期肝脏恶性肿瘤中的疗效及生活质量评估[J].现代医学,2021,49(6):623-629.
[3] ATUN R,JAFFRAY D A,BARTON M B,et al.Expanding global access to radiotherapy[J].Lancet Oncol,2015,16(10):1153-1186.
[4] KLOPP A H,YEUNG A R,DESHMUKH S,et al.Patient-reported toxicity during pelvic intensity-modulated radiation therapy:NRG Oncology-RTOG 1203[J].J Clin Oncol,2018,36(24):2538-2544.
[5] DAHIYA D S,KICHLOO A,TUMA F,et al.Radiation proctitis and management strategies[J].Clin Endosc,2022,55(1):22-32.
[6] KIM K T,CHAE H S,KIM J S,et al.Thalidomide effect in endothelial cell of acute radiation proctitis[J].World J Gastroenterol,2008,14(30):4779-4783.
[7] FAN T W,HIGASHI R M,LANE A N.Integrating metabolomics and transcriptomics for probing SE anticancer mechanisms[J].Drug Metab Rev,2006,38(4):707-732.
[8] WIKOFF W R,GANGOITI J A,BARSHOP B A,et al.Metabolomics identifies perturbations in human disorders of propionate metabolism[J].Clin Chem,2007,53(12):2169-2176.
[9] WU H,XUE R,LU C,et al.Metabolomic study for diagnostic model of oesophageal cancer using gas chromatography/mass spectrometry[J].J Chromatogr B Analyt Technol Biomed Life Sci,2009,877(27):3111-3117.
[10] ANDREYEV H J,VLAVIANOS P,BLAKE P,et al.Gastrointestinal symptoms after pelvic radiotherapy:role for the gastroenterologist?[J].Int J Radiat Oncol Biol Phys,2005,62(5):1464-1471.
[11] 汤福想,郎凯楠,刘玉玲.PAX1和ZNF582甲基化在宫颈细胞学非典型鳞状细胞分层管理中的意义[J].中国生育健康杂志,2020,31(4):345-349,357.
[12] COX J D,STETZ J,PAJAK T F.Toxicity criteria of the Radiation Therapy Oncology Group(RTOG) and the European Organization for Research and Treatment of Cancer(EORTC)[J].Int J Radiat Oncol Biol Phys,1995,31(5):1341-1346.
[13] YANG C,LIU S,LI H,et al.The effects of psyllium husk on gut microbiota composition and function in chronically constipated women of reproductive age using 16S rRNA gene sequencing analysis[J].Aging(Albany NY),2021,13(11):15366-15383.
[14] GREMY O,BENDERITTER M,LINARD C.Acute and persisting Th2-like immune response after fractionated colorectal gamma-irradiation[J].World J Gastroenterol,2008,14(46):7075-7085.
[15] KALITA B,RANJAN R,GUPTA M L.Combination treatment of podophyllotoxin and rutin promotes mouse Lgr5(+ve) intestinal stem cells survival against lethal radiation injury through Wnt signaling[J].Apoptosis,2019,24(3-4):326-340.
[16] GERASSY-VAINBERG S,BLATT A,DANIN-POLEG Y,et al.Radiation induces proinflammatory dysbiosis:transmission of inflammatory susceptibility by host cytokine induction[J].Gut,2018,67(1):97-107.
[17] WANG Z,WANG Q,WANG X,et al.Gut microbial dysbiosis is associated with development and progression of radiation enteritis during pelvic radiotherapy[J].J Cell Mol Med,2019,23(5):3747-3756.
[18] 余祥坤,刘坤,李志鹏,等.铜/凹凸棒石复合材料高效吸附放射性碘离子性能[J].无机材料学报,2021,36(8):856-864.
[19] CRAWFORD P A,GORDON J I.Microbial regulation of intestinal radiosensitivity[J].Proc Natl Acad Sci U S A,2005,102(37):13254-13259.
[20] CAROLIEN O,ANNE V,LISANNE J,et al.PS14-68.Differential effects of antibiotics on bile acid metabolism,intestinal microbiota composition and insulin resistance in obese humans; a randomised controlled trial[J].Nederlands Tijdschrift Voor Diabetologie,2015,10(3):147.
[21] MANICHANH C,VARELA E,MARTINEZ C,et al.The gut microbiota predispose to the pathophysiology of acute postradiotherapy diarrhea[J].Am J Gastroenterol,2008,103(7):1754-1761.
[22] MEDRANO A Y D,COLBERT L E,HUTCHINSON D L,et al.Increased diversity of the intestinal microbiome predicts for lower rates of patient reported acute gastrointestinal toxicity in women receiving radiation therapy for cervical cancer[J].International Journal of Radiation Oncology,Biology,Physics,2017,99(2):111-112.
[23] THOMPSON R,GEBHART C J,ARMIEN A G,et al.Fatal suppurative inflammation in daurian pikas(ochotona dauurica)naturally infected with castellaniella ginsengisoli-like bacteria[J].Journal of Zoo and Wildlife Medicine,2015,46(3):560-564.
[24] 李思聪,李玉明.肠复康方对急性放射性肠炎大鼠一般情况及小肠黏膜炎性因子的影响[J].中国中西医结合消化杂志,2016,24(8):594-599.
[25] 李宜放,王晞星,刘丽坤,等.肠瑞灌肠剂对放射性直肠炎大鼠IL-1β及NF-κB表达的影响[J].肿瘤研究与临床,2008,20(10):665-668.
[26] GERASSY-VAINBERG S,BLATT A,DANIN-POLEG Y,et al.Radiation induces proinflammatory dysbiosis:transmission of inflammatory susceptibility by host cytokine induction[J].Gut,2018,67(1):97-107.
[27] WANG Y,WANG L,GONG Z.Regulation of acetylation in high mobility group protein B1 cytosol translocation[J].DNA Cell Biol,2019,38(5):491-499.
[28] 蔡妩扬,蒋骏航,钱峰.HMGB1研究进展[J].上海医药,2019,40(3):60-63.
[29] ABOYOUSSEF A M,MOHAMMAD M K,ABO-SAIF A A,et al.Granisetron attenuates liver injury and inflammation in a rat model of cecal ligation and puncture-induced sepsis[J].Pharmacol Sci,2021,147(4):358-366.

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