Individuality and generality of intratumoral microbiome in the three most prevalent gynecological malignancies: an observational study

Author:

Xiao Qin1,Chen Wen-jie23ORCID,Wu Fei1,Zhang Xin-yi2,Li Xia4,Wei Jing3,Chen Ting-tao135ORCID,Liu Zhao-xia1ORCID

Affiliation:

1. Departments of Reproductive Medicine, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, China

2. Queen Mary School, Jiangxi Medical College, Nanchang University, Nanchang, China

3. National Engineering Research Center for Bioengineering Drugs and the Technologies, Institution of Translational Medicine, Jiangxi Medical College, Nanchang University, Nanchang, China

4. Department of Assisted Reproduction, Maternity and Child Health Hospital of Jiujiang, Jiujiang, Jiangxi, China

5. School of Pharmacy, Jiangxi Medical College, Nanchang University, Nanchang, China

Abstract

ABSTRACT Growing evidence have indicated the crucial role of intratumor microbiome in a variety of solid tumor. However, the intratumoral microbiome in gynecological malignancies is largely unknown. In the present study, a total of 90 Han patients, including 30 patients with cancer in cervix, ovary, and endometrium each were enrolled, the composition of intratumoral microbiome was assessed by 16S rDNA amplicon high throughput sequencing. We found that the diversity and metabolic potential of intratumoral microbiome in all three cancer types were very similar. Furthermore, all three cancer types shared a few taxa that collectively take up high relative abundance and positive rate, including Pseudomonas sp ., Comamonadaceae gen. sp ., Bradyrhizobium sp ., Saccharomonospora sp ., Cutibacterium acnes , Rubrobacter sp ., Dialister micraerophilus , and Escherichia coli . Additionally, Haemophilus parainfluenzae and Paracoccus sp . in cervical cancer, Pelomonas sp . in ovarian cancer, and Enterococcus faecalis in endometrial cancer were identified by LDA to be a representative bacterial strain. In addition, in cervical cancer patients, alpha-fetoprotein (AFP) (correlation coefficient = −0.3714) was negatively correlated ( r = 0.4, 95% CI: 0.03 to 0.7) with Rubrobacter sp . and CA199 (correlation coefficient = 0.3955) was positively associated ( r = 0.4, 95% CI: 0.03 to 0.7) with Saccharomonospora sp .. In ovarian cancer patients, CA125 (correlation coefficient = −0.4451) was negatively correlated ( r = −0.4, 95% CI: −0.7 to −0.09) with Porphyromonas sp. . In endometrial cancer patients, CEA (correlation coefficient = −0.3868) was negatively correlated ( r = −0.4, 95% CI: −0.7 to −0.02) with Cutibacterium acnes . This study promoted our understanding of the intratumoral microbiome in gynecological malignancies. IMPORTANCE In this study, we found the compositional spectrum of tumor microbes among gynecological malignancies were largely similar by sharing a few taxa and differentiated by substantial species owned uniquely. Certain species, mostly unreported, were identified to be associated with clinical characteristics. This study prompted our understanding of gynecological malignancies and offered evidence for tumor microbes affecting tumor biology among cancers in the female reproductive system.

Funder

MOST | National Natural Science Foundation of China

Jiangxi Province Key Laboratory of bioengineering drugs

Publisher

American Society for Microbiology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3