Evidence map›Paper›PMID 36258167›Full record

ArticleBMC cancer2022

Distribution of microbiota in cervical preneoplasia of racially disparate populations.

Kunwar Somesh Vikramdeo, Shashi Anand, Jennifer Young Pierce, Ajay Pratap Singh, Seema Singh, Santanu Dasgupta

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 38% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. iScience · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Kunwar Somesh VikramdeoMitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
Shashi AnandMitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
Jennifer Young PierceMitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
Ajay Pratap SinghMitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
Seema SinghMitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA.
Santanu DasguptaMitchell Cancer Institute, University of South Alabama, Mobile, AL, 36604, USA. dasgupta@southalabama.edu.
University of South Alabama · USUSA Mitchell Cancer Institute · US

Funding

Impact of social factors on breast cancer biology in African-American womenR01CA231925 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI SINGH, SEEMA · 2019 to 2023
$3.0M
A novel molecular cross-talk driving pancreatic cancer progressionR01CA224306 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI SINGH, AJAY PRATAP · 2018 to 2022
$1.7M
NCI NIH HHS R01 CA224306NCI NIH HHS R01 CA231925NIH HHS CA231925, CA224306
6 · The paper itself

Abstract

backgroundsMicrobiome 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.

methodsHere, 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).

resultsWe 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.

conclusionsMicrobial 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.

Indexed as

MicrobiotaPapillomavirus InfectionsUterine Cervical DysplasiaUterine Cervical NeoplasmsDysbiosisFemaleHumansPapillomaviridaeRNA, Ribosomal, 16SRNA, Ribosomal, 16SCancer riskCervixHPVMicrobiomePreneoplasia

Identifiers

PMID36258167
PMCPMC9578267
OpenAlexW4306685602

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.