Department of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States of America.
Gynecol Oncol. 2019 Nov;155(2):237-244. doi: 10.1016/j.ygyno.2019.09.002. Epub 2019 Sep 26.
The aim of this study was to characterize variation in the gut microbiome of women with locally advanced cervical cancer and compare it to healthy controls.
We characterized the 16S rDNA fecal microbiome in 42 cervical cancer patients and 46 healthy female controls. Shannon diversity index (SDI) was used to evaluate alpha (within sample) diversity. Beta (between sample) diversity was examined using principle coordinate analysis (PCoA) of unweighted Unifrac distances. Relative abundance of microbial taxa was compared between samples using Linear Discriminant Analysis Effect Size (LEfSe).
Within cervical cancer patients, bacterial alpha diversity was positively correlated with age (p = 0.22) but exhibited an inverse relationship in control subjects (p < 0.01). Alpha diversity was significantly higher in cervical cancer patients as compared to controls (p < 0.05), though stratification by age suggested this relationship was restricted to older women (>50 years; p < 0.01). Beta diversity (unweighted Unifrac; p < 0.01) also significantly differed between cervical cancer patients and controls. Based on age- and race-adjusted LEfSe analysis, multiple taxa significantly differed between cervical cancer patients and controls. Prevotella, Porphyromonas, and Dialister were significantly enriched in cervical cancer patients, while Bacteroides, Alistipes and members of the Lachnospiracea family were significantly enriched in healthy subjects.
Our study suggests differences in gut microbiota diversity and composition between cervical cancer patients and controls. Associations within the gut microbiome by age may reflect etiologic/clinical differences. These findings provide rationale for further study of the gut microbiome in cervical cancer.
本研究旨在分析局部晚期宫颈癌患者肠道微生物组的变异性,并将其与健康对照进行比较。
我们对 42 例宫颈癌患者和 46 例健康女性对照者的粪便 16S rDNA 微生物组进行了特征分析。采用 Shannon 多样性指数(SDI)评估α(样本内)多样性。采用无权重 Unifrac 距离的主坐标分析(PCoA)来研究β(样本间)多样性。使用线性判别分析效应量(LEfSe)比较样本中微生物类群的相对丰度。
在宫颈癌患者中,细菌 α 多样性与年龄呈正相关(p=0.22),但在对照组中呈负相关(p<0.01)。与对照组相比,宫颈癌患者的 α 多样性显著更高(p<0.05),但分层分析表明这种关系仅限于年龄较大的女性(>50 岁;p<0.01)。β 多样性(无权重 Unifrac;p<0.01)也在宫颈癌患者和对照组之间存在显著差异。基于年龄和种族调整的 LEfSe 分析,宫颈癌患者和对照组之间有多个分类群存在显著差异。普雷沃氏菌属、卟啉单胞菌属和戴阿利斯特菌属在宫颈癌患者中明显富集,而拟杆菌属、阿里斯泰普斯菌属和lachnospiracea 家族的成员在健康受试者中明显富集。
我们的研究表明宫颈癌患者和对照组之间的肠道微生物多样性和组成存在差异。肠道微生物组内的年龄相关性可能反映了病因/临床差异。这些发现为进一步研究宫颈癌患者的肠道微生物组提供了依据。