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不同种族人群宫颈上皮内瘤变中微生物群的分布。

Distribution of microbiota in cervical preneoplasia of racially disparate populations.

机构信息

Mitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.

Department of Pathology, College of Medicine, Mitchell Cancer Institute, University of South Alabama, 1660 Springhill Avenue, Mobile, AL, 36604, USA.

出版信息

BMC Cancer. 2022 Oct 18;22(1):1074. doi: 10.1186/s12885-022-10112-6.

DOI:10.1186/s12885-022-10112-6
PMID:36258167
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9578267/
Abstract

BACKGROUNDS

Microbiome dysbiosis is an important contributing factor in tumor development and thus may be a risk predictor for human malignancies. In the United States, women with Hispanic/Latina (HIS) and African American (AA) background have a higher incidence of cervical cancer and poorer outcomes than Caucasian American (CA) women.

METHODS

Here, we assessed the distribution pattern of microbiota in cervical intraepithelial neoplasia (CIN) lesions obtained from HIS (n = 12), AA (n = 12), and CA (n = 12) women, who were screened for CC risk assessment. We employed a 16S rRNA gene sequencing approach adapted from the NIH-Human Microbiome Project to identify the microbial niche in all CIN lesions (n = 36).

RESULTS

We detected an appreciably decreased abundance of beneficial Lactobacillus in the CIN lesions of the AA and HIS women compared to the CA women. Differential abundance of potentially pathogenic Prevotella, Delftia, Gardnerella, and Fastidiosipila was also evident among the various racial groups. An increased abundance of Micrococcus was also evident in AA and HIS women compared to the CA women. The detection level of Rhizobium was higher among the AA ad CA women compared to the HIS women. In addition to the top 10 microbes, a unique niche of 27 microbes was identified exclusively in women with a histopathological diagnosis of CIN. Among these microbes, a group of 8 microbiota; Rubellimicrobium, Podobacter, Brevibacterium, Paracoccus, Atopobium, Brevundimonous, Comamonous, and Novospingobium was detected only in the CIN lesions obtained from AA and CA women.

CONCLUSIONS

Microbial dysbiosis in the cervical epithelium represented by an increased ratio of potentially pathogenic to beneficial microbes may be associated with increased CC risk disparities. Developing a race-specific reliable panel of microbial markers could be beneficial for CC risk assessment, disease prevention, and/or therapeutic guidance.

摘要

背景

微生物组失调是肿瘤发生的一个重要因素,因此可能是人类恶性肿瘤的风险预测因子。在美国,西班牙裔/拉丁裔(HIS)和非裔美国人(AA)背景的女性宫颈癌发病率较高,预后较白种人美国女性(CA)差。

方法

在这里,我们评估了来自 HIS(n=12)、AA(n=12)和 CA(n=12)女性的宫颈上皮内瘤变(CIN)病变中微生物群的分布模式,这些女性是为了 CC 风险评估而筛选的。我们采用了一种来自 NIH-Human Microbiome Project 的 16S rRNA 基因测序方法来识别所有 CIN 病变(n=36)中的微生物生态位。

结果

我们检测到 AA 和 HIS 女性的 CIN 病变中有益的乳酸杆菌丰度明显降低,而 CA 女性则没有。在不同的种族群体中,也可以明显观察到潜在致病性的普雷沃氏菌、德尔福蒂氏菌、加德纳菌和 Fastidiosipila 的差异丰度。与 CA 女性相比,AA 和 HIS 女性的微球菌丰度也明显增加。与 HIS 女性相比,AA 和 CA 女性的根瘤菌检测水平更高。除了前 10 种微生物外,还在组织病理学诊断为 CIN 的女性中鉴定出了一个独特的 27 种微生物生态位。在这些微生物中,一组 8 种微生物;Rubellimicrobium、Podobacter、Brevibacterium、Paracoccus、Atopobium、Brevundimonous、Comamonous 和 Novospingobium 仅在 AA 和 CA 女性的 CIN 病变中被检测到。

结论

以潜在致病性与有益微生物比例增加为代表的宫颈上皮微生物失调可能与增加的 CC 风险差异有关。开发特定种族的可靠微生物标志物面板可能有助于 CC 风险评估、疾病预防和/或治疗指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/9578267/fa5f10a03baa/12885_2022_10112_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/9578267/ad7c8c66f86b/12885_2022_10112_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/9578267/38e83afb0867/12885_2022_10112_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/9578267/17a9aac1d4c5/12885_2022_10112_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/9578267/5d7d9aa0573a/12885_2022_10112_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/9578267/79be67145fc4/12885_2022_10112_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/9578267/fa5f10a03baa/12885_2022_10112_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/9578267/ad7c8c66f86b/12885_2022_10112_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/9578267/38e83afb0867/12885_2022_10112_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/9578267/17a9aac1d4c5/12885_2022_10112_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/9578267/5d7d9aa0573a/12885_2022_10112_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/9578267/79be67145fc4/12885_2022_10112_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/9578267/fa5f10a03baa/12885_2022_10112_Fig6_HTML.jpg

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