# Stool and vaginal microbiome profiles patterns among Black and White endometrial cancer survivors: A pilot study in North Carolina

**Authors:** Mu Jin, Temitope Keku, Amber McCoy, Jordyn A. Brown, Marc Peterson, Jamie Hunter, Shawn Smith, Stephenie Black-Grant, Melinda S. Yates, Anne F. Peery, Victoria L. Bae-Jump, M. Andrea Azcarate-Peril, Stephanie M. Engel, Andrew F. Olshan, Hazel B. Nichols

PMC · DOI: 10.1371/journal.pone.0336772 · PLOS One · 2026-01-23

## TL;DR

This pilot study explores how cancer treatments affect the vaginal and gut microbiomes of endometrial cancer survivors, finding that chemotherapy and radiation may reduce Lactobacillus and increase microbial diversity.

## Contribution

The study is the first to compare stool and vaginal microbiome profiles in Black and White endometrial cancer survivors and assess self-sampling feasibility.

## Key findings

- Vaginal microbiome diversity increased after chemotherapy or radiation compared to surgery alone.
- Lactobacillus dominance was lower in the chemotherapy or radiation group compared to the surgery-only group.
- Self-collection of stool and vaginal samples was found to be feasible and acceptable among participants.

## Abstract

Endometrial cancer is the most common gynecologic cancer in the US. Endometrial cancer survivors may experience changes in microbiome due to cancer treatment and other factors. The human microbiome plays a crucial role in maintaining the proper functioning of the body. A more diverse microbiome often indicates a healthier gut environment, while lower vaginal microbiome diversity, specifically a Lactobacillus-dominant vagitype, is associated with more favorable health outcomes. The objectives of this pilot study were to evaluate potential variation in stool and vaginal microbiome communities and to assess the feasibility and acceptability of self-sampling among endometrial cancer survivors.

Endometrial cancer survivors (N = 50) enrolled in the Carolina Endometrial Cancer Study, a cohort of women diagnosed with endometrial cancer, were mailed Genotek vaginal swab and stool self-collection kits. Self-reported questionnaires assessed information on survivors’ demographics, sexual and bowel function, and perspectives on the self-sampling processes. Tumor characteristics and cancer treatment information were assessed from medical records. Microbiota profiles were characterized by bacteria 16S rRNA amplicon sequencing.

Overall, 48 vaginal swabs and 47 stool samples were obtained. Alpha (Shannon p = 0.04) and beta (Bray-Curtis p = 0.004) diversity of vaginal microbiome samples varied by cancer treatment, with higher microbial diversity after chemotherapy or radiation compared to surgery alone. In the surgery only group, 63% of samples were Lactobacillus-dominant compared to 17% among the chemotherapy or radiation group. Stool microbiome diversity did not vary by cancer treatment status. No statistically significant differences in alpha or beta diversity were observed in either vaginal or stool microbiome communities across racial subgroups or by sexual or bowel function.

Self-collection of stool and vaginal microbiome samples is feasible and acceptable in cancer survivors. Our results suggest that radiation and chemotherapy for endometrial cancer may decrease the abundance of beneficial Lactobacillus and increase less favorable vaginal microbial diversity among endometrial cancer survivors.

## Linked entities

- **Diseases:** endometrial cancer (MONDO:0002447)

## Full-text entities

- **Diseases:** Non-endometrioid disease (MESH:D018269), sexually transmitted infections (MESH:D012749), preterm birth (MESH:D047928), dysbiosis (MESH:D064806), cervical lesions (MESH:D002575), cervical cancer (MESH:D002583), bowel (MESH:D012778), uterine cancer (MESH:D014594), Colorectal-Anal Distress (MESH:D015179), fecal incontinence (MESH:D005242), pain (MESH:D010146), inflammation (MESH:D007249), Pelvic Floor (MESH:D059952), serous tumors (MESH:D018297), yeast infections (MESH:D002181), Endometrial Cancer (MESH:D016889), gynecologic malignancies (MESH:D005833), infection (MESH:D007239), obesity (MESH:D009765), vaginal dryness (MESH:D014627), bacterial vaginosis (MESH:D016585), Cancer (MESH:D009369), inflammatory bowel diseases (MESH:D015212), bleeding (MESH:D006470), genitourinary or gastrointestinal side effects (MESH:D064420), dryness (MESH:D014987)
- **Chemicals:** acetic acid (MESH:D019342), lactic acid (MESH:D019344)
- **Species:** PX clade (clade) [taxon 569578], Gardnerella (genus) [taxon 2701], Homo sapiens (human, species) [taxon 9606], Bacteroides (genus) [taxon 816], Lactobacillus (genus) [taxon 1578], gut metagenome (species) [taxon 749906], Bifidobacterium (genus) [taxon 1678], Anaerococcus (genus) [taxon 165779], Blautia (genus) [taxon 572511], Porphyromonas (genus) [taxon 836], Mobiluncus (genus) [taxon 2050], Prevotella (genus) [taxon 838]

## Full text

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## Figures

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## References

86 references — full list in the complete paper: https://tomesphere.com/paper/PMC12829856/full.md

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Source: https://tomesphere.com/paper/PMC12829856