Volume 5, Issue 1-2 pp. 14-34
REVIEW
Open Access

The Gut Microbiome in Aging and Ovarian Cancer

Gena M. Dominique

Gena M. Dominique

Department of Chemistry and Biochemistry, Harper Cancer Research Institute, University of Notre Dame, Notre Dame, Indiana, USA

Contribution: Conceptualization (equal), Funding acquisition (equal), ​Investigation (equal), Project administration (equal), Visualization (lead), Writing - original draft (lead), Writing - review & editing (lead)

Search for more papers by this author
Catherine Hammond

Catherine Hammond

Department of Biology, University of Notre Dame, Notre Dame, Indiana, USA

Contribution: ​Investigation (supporting), Writing - original draft (supporting), Writing - review & editing (supporting)

Search for more papers by this author
M. Sharon Stack

Corresponding Author

M. Sharon Stack

Department of Chemistry and Biochemistry, Harper Cancer Research Institute, University of Notre Dame, Notre Dame, Indiana, USA

Correspondence: M. Sharon Stack ([email protected])

Contribution: Conceptualization (equal), Funding acquisition (lead), Writing - review & editing (equal)

Search for more papers by this author
First published: 20 June 2024

Funding: This research was funded by National Institutes of Health/National Cancer Institute (Grants RO1CA109545 [M.S.S.] and UO1CA236979 [M.S.S.]), the Samuel Waxman Cancer Research Foundation (M.S.S.), and the Dolores Zohrab Liebmann Fund (G.M.D.).

ABSTRACT

The gut microbiome changes with age and affects regions beyond the gut, including the ovarian cancer tumor microenvironment. In this review summarizing the literature on the gut microbiome in ovarian cancer and in aging, we note trends in the microbiota composition common to both phenomena and trends that are distinctly opposite. Both ovarian cancer and aging are characterized by an increase in proinflammatory bacterial species, particularly those belonging to phylum Proteobacteria and genus Escherichia, and a decrease in short-chain fatty acid producers, particularly those in Clostridium cluster XIVa (family Lachnospiraceae) and the Actinobacteria genus Bifidobacterium. However, although beneficial bacteria from family Porphyromonadaceae and genus Akkermansia tend to increase with normal, healthy aging, these bacteria tend to decrease in ovarian cancer, similar to what is observed in obesity or unhealthy aging. We also note a lack in the current literature of research demonstrating causal relationships between the gut microbiome and ovarian cancer outcomes and research on the gut microbiome in ovarian cancer in the context of aging, both of which could lead to improvements to ovarian cancer diagnosis and treatment.

Conflicts of Interest

The authors declare no conflicts of interest.

Data Availability Statement

The authors have nothing to report.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.