Evidence map›Paper›PMID 40575364›Full record

ArticleWorld journal of gastrointestinal pharmacology and therapeutics2025

Exploring the gut microbiome's influence on cancer-associated anemia: Mechanisms, clinical challenges, and innovative therapies.

Ayrton Bangolo, Behzad Amoozgar, Maryam Habibi, Elizabeth Simms, Vignesh K Nagesh, Shruti Wadhwani, Nikita Wadhwani, Auda Auda, Daniel Elias, Charlene Mansour and 8 more

Abstract read
In one paragraph

Article in World journal of gastrointestinal pharmacology and therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Microbiome-derived metabolites in cancer-associated anemia: An underexplored mechanistic link.World journal of gastrointestinal pharmacology and therapeutics · 2025
    Article
  6. Review
  7. Review
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

18 authors.

Ayrton BangoloDepartment of Hematology and Oncology, John Theurer Cancer Center, Hackensack, NJ 07601, United States. ayrton.bangolo@hmhn.org.
Behzad AmoozgarDepartment of Hematology and Oncology, John Theurer Cancer Center, Hackensack, NJ 07601, United States.
Maryam HabibiDepartment of Research, Tulane National Primate Research Center, Covington, LA 70433, United States.
Elizabeth SimmsDepartment of Medicine, Wake Forest University School of Medicine, Winston-Salem, NC 27101, United States.
Vignesh K NageshDepartment of Internal Medicine, Hackensack Palisades Medical Center, North Bergen, NJ 07047, United States.
Shruti WadhwaniDepartment of Internal Medicine, Hackensack Palisades Medical Center, North Bergen, NJ 07047, United States.
Nikita WadhwaniDepartment of Internal Medicine, Hackensack Palisades Medical Center, North Bergen, NJ 07047, United States.
Auda AudaDepartment of Family Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Daniel EliasDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Charlene MansourDepartment of Internal Medicine, Palisades Medical Center, North Bergen, NJ 07047, United States.
Robert AbbottRutgers New Jersey Medical School, Newark, NJ 07103, United States.
Nisrene JebaraColumbia University School of Nursing, New York, NY 10032, United States.
Lili ZhangDepartment of Hematology and Oncology, John Theurer Cancer Center, Hackensack, NJ 07601, United States.
Sarvarinder GillDepartment of Hematology and Oncology, John Theurer Cancer Center, Hackensack, NJ 07601, United States.
Kareem AhmedDepartment of Medicine, University of Washington, Seattle, WA 98195, United States.
Andrew IpDivision of Lymphoma, John Theurer Cancer Center, Hackensack, NJ 07601, United States.
Andre GoyDivision of Lymphoma, John Theurer Cancer Center, Hackensack, NJ 07601, United States.
Christina ChoDivision of Stem Cell Transplant and Cellular Therapy, John Theurer Cancer Center, Hackensack, NJ 07601, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAnemia is a prevalent and challenging complication in patients with hematologic and solid malignancies, which stems from the direct effects of malignancy, treatment-induced toxicities, and systemic inflammation. It affects patients' survival, functional status, and quality of life profoundly. Recent literature has highlighted the emerging role of the gut microbiome in the pathogenesis of cancer-associated anemia. The gut microbiota, through its intricate interplay with iron metabolism, inflammatory pathways, and immune modulation, may either exacerbate or ameliorate anemia depending on its composition, and functional integrity. Dysbiosis, characterized by disruption in the gut microbial ecosystem, is very common in cancer patients. This microbial imbalance is implicated in anemia causation through diminished iron absorption, persistent low-grade inflammation, and suppression of erythropoiesis.

aimTo consolidate current evidence regarding the interplay between gut microbiome and anemia in the setting of malignancies. It aims to provide a detailed exploration of the mechanistic links between dysbiosis and anemia, identifies unique challenges associated with various cancer types, and evaluates the efficacy of microbiome-focused therapies. Through this integrative approach, the review seeks to establish a foundation for innovative clinical strategies aimed at mitigating anemia and improving patient outcomes in oncology.

methodsA literature search was performed using multiple databases, including Google Scholar, PubMed, Scopus, and Web of Science, using a combination of keywords and Boolean operators to refine results. Keywords included "cancer-associated anemia", "gut microbiome", "intestinal microbiota", "iron metabolism", "gut dysbiosis", "short-chain fatty acids", "hematopoiesis", "probiotics", "prebiotics", and "fecal microbiota transplantation". Articles published in English between 2000 and December 2024 were included, with a focus on contemporary and relevant findings.

resultsTherapeutic strategies aimed at restoration of gut microbial homeostasis, such as probiotics, prebiotics, dietary interventions, and fecal microbiota transplantation (FMT), can inhibit anemia-causing pathways by enhancing microbial diversity, suppressing detrimental flora, reducing systemic inflammation and optimizing nutrient absorption.

conclusionGut dysbiosis causes anemia and impairs response to chemotherapy in cancer patients. Microbiome-centered interventions, such as probiotics, prebiotics, dietary modifications, and FMT, have shown efficacy in restoring microbial balance, reducing inflammation, and enhancing nutrient bioavailability. Emerging approaches, including engineered probiotics and bacteriophage therapies, are promising precision-based, customizable solutions for various microbiome compositions and imbalances. Future research should focus on integrating microbiome-targeted strategies with established anemia therapies.

Indexed as

Cancer-associated anemiaDysbiosisGut microbiomeIron metabolismMicrobiome-targeted therapiesSystemic inflammation

Identifiers

PMID40575364
PMCPMC12188820

What Socratic holds

Textmetadata
LicenceCC BY-NC
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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 Socratic graph.