» Articles » PMID: 32057462

Gut Microbiota Differences in Island Hispanic Puerto Ricans and Mainland Non-Hispanic Whites During Chemoradiation for Rectal Cancer: A Pilot Study

Overview
Specialty Oncology
Date 2020 Feb 15
PMID 32057462
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: To investigate whether there are differences in diversity, taxonomic composition, and predicted functional pathways of the gut microbiome between Island Hispanic Puerto Ricans (HPR) and mainland non-Hispanic whites (NHW) measured before and at the end of chemo-radiation (CRT) for Rectal Cancer.

Methods: Fifty-six stool samples of newly diagnosed rectal cancer patients (25 HPR and 31 NHW) were amplicon-sequenced during chemo-radiotherapy. 16S rRNA gene data was analyzed using QIIME2, phyloseq, and LEfSe.

Results: We observed similar within-sample alpha diversity for HPR and NHW participants during CRT. However, at the end of CRT, several taxa were present at significantly different abundances across both groups. Taxa enriched in the gut of HPR compared to NHW included Muribaculaceae, Prevotella 2 and 7, Gemella, Bacillales Family XI, Catenibacterium, Sutterella, Pasteurellales, and Pasteurellaceae genera, whereas over-represented taxa in NHW participants were Turicibacter and Eubacteriaceae. Significant differences in predicted HPR microbiota functions included pathways for synthesis of L-methionine and degradation of phenylethylamine and phenylacetate.

Conclusion: In this pilot study, taxonomic analyses and functional predictions of the gut microbiomes suggest greater inflammatory potential in gut microbial functions among HPR rectal cancer patients undergoing CRT compared to that of NHW participants.

Citing Articles

Integrating clinical and cross-cohort metagenomic features: a stable and non-invasive colorectal cancer and adenoma diagnostic model.

Zhou D, Chen Y, Wang Z, Zhu S, Zhang L, Song J Front Mol Biosci. 2024; 10:1298679.

PMID: 38455360 PMC: 10919151. DOI: 10.3389/fmolb.2023.1298679.


The human microbiome links to prostate cancer risk and treatment (Review).

Xia B, Wang J, Zhang D, Hu X Oncol Rep. 2023; 49(6).

PMID: 37144511 PMC: 10196737. DOI: 10.3892/or.2023.8560.


Gut Microbiota and Depressive Symptoms at the End of CRT for Rectal Cancer: A Cross-Sectional Pilot Study.

Gonzalez-Mercado V, Lim J, Saligan L, Perez N, Rodriguez C, Bernabe R Depress Res Treat. 2022; 2021:7967552.

PMID: 35003805 PMC: 8731300. DOI: 10.1155/2021/7967552.


Gut Microbiome and Its Associations With Acute and Chronic Gastrointestinal Toxicities in Cancer Patients With Pelvic Radiation Therapy: A Systematic Review.

Bai J, Barandouzi Z, Rowcliffe C, Meador R, Tsementzi D, Bruner D Front Oncol. 2021; 11:745262.

PMID: 34938654 PMC: 8685326. DOI: 10.3389/fonc.2021.745262.


Factors Affecting the Severity of Fatigue during Radiotherapy for Prostate Cancer; an Exploratory Study.

Gonzalez-Mercado V, Marrero S, Marrero-Falcon M, Saligan L Urol Nurs. 2021; 40(3):129-138.

PMID: 34220179 PMC: 8248518.

References
1.
Carson T, Wang F, Cui X, Jackson B, van Der Pol W, Lefkowitz E . Associations Between Race, Perceived Psychological Stress, and the Gut Microbiota in a Sample of Generally Healthy Black and White Women: A Pilot Study on the Role of Race and Perceived Psychological Stress. Psychosom Med. 2018; 80(7):640-648. PMC: 6113071. DOI: 10.1097/PSY.0000000000000614. View

2.
Giordano A, Dincman T, Clyburn B, Steed L, Rockey D . Clinical Features and Outcomes of Pasteurella multocida Infection. Medicine (Baltimore). 2015; 94(36):e1285. PMC: 4616664. DOI: 10.1097/MD.0000000000001285. View

3.
McMurdie P, Holmes S . phyloseq: an R package for reproducible interactive analysis and graphics of microbiome census data. PLoS One. 2013; 8(4):e61217. PMC: 3632530. DOI: 10.1371/journal.pone.0061217. View

4.
Barton L, Ritz N, Fauque G, Lin H . Sulfur Cycling and the Intestinal Microbiome. Dig Dis Sci. 2017; 62(9):2241-2257. DOI: 10.1007/s10620-017-4689-5. View

5.
Chiku T, Padovani D, Zhu W, Singh S, Vitvitsky V, Banerjee R . H2S biogenesis by human cystathionine gamma-lyase leads to the novel sulfur metabolites lanthionine and homolanthionine and is responsive to the grade of hyperhomocysteinemia. J Biol Chem. 2009; 284(17):11601-12. PMC: 2670165. DOI: 10.1074/jbc.M808026200. View