# Fecal microbiota transplantation: a novel strategy and challenges in the adjuvant treatment of bladder Cancer

**Authors:** Xinwei Liu, Zhiqiang Chen, Yichen Lu, Yifan Wu, Yongneng Huang, Yuwei Zhang, Menglu Li, Ninghan Feng

PMC · DOI: 10.3389/fmicb.2026.1756107 · 2026-02-03

## TL;DR

This review explores fecal microbiota transplantation (FMT) as a potential new adjuvant treatment for bladder cancer, focusing on its role in improving therapy effectiveness and addressing challenges in clinical management.

## Contribution

The paper systematically reviews the potential of FMT as an innovative adjuvant strategy for bladder cancer treatment.

## Key findings

- Gut microbiota dysbiosis is linked to bladder cancer progression and treatment response.
- FMT may enhance therapy effectiveness by modulating microbial metabolites and the intestinal barrier.
- Combining FMT with existing therapies like immunotherapy could offer new treatment avenues.

## Abstract

The clinical management of bladder cancer faces major challenges due to treatment resistance and recurrence, which require the development of new adjuvant strategies. The role of the gut microbiome in influencing bladder cancer progression and treatment response through the “gut-bladder axis” is gaining recognition. This understanding provides a theoretical rationale for exploring microbiota-targeting interventions, such as fecal microbiota transplantation (FMT). As a method capable of thoroughly reshaping the gut microbiota, FMT may have broad clinical potential. This review systematically explores the possible role of FMT in treating bladder cancer. It begins by summarizing the observational and causal evidence linking gut microbiota dysbiosis to bladder cancer, which forms the rationale for considering FMT as an intervention. Then, it discusses how FMT might improve therapeutic effectiveness, including regulation of microbial metabolites (such as short-chain fatty acids, tryptophan, and bile acids), repair of the intestinal barrier, induction of epigenetic reprogramming and modulation of the urinary microbiota. The review also considers potential scenarios for combining FMT with existing adjuvant therapies, including immunotherapy, chemotherapy, and radiotherapy. Finally, it objectively evaluates the key challenges in translating FMT into clinical practice, including effectiveness, safety, standardization, and regulatory or ethical issues, and outlines future directions. By synthesizing current evidence, this review highlights FMT as a potentially promising and innovative adjuvant strategy worthy of further investigation, which, if validated, could contribute to overcoming current therapeutic challenges in bladder cancer.

## Linked entities

- **Chemicals:** tryptophan (PubChem CID 1148)
- **Diseases:** bladder cancer (MONDO:0004986)

## Full-text entities

- **Genes:** IDO1 (indoleamine 2,3-dioxygenase 1) [NCBI Gene 3620] {aka IDO, IDO-1, INDO}, LINC00858 (long intergenic non-protein coding RNA 858) [NCBI Gene 170425] {aka CRCAL-2, LNMAT2}, MAP2K7 (mitogen-activated protein kinase kinase 7) [NCBI Gene 5609] {aka JNKK2, MAPKK7, MEK, MEK 7, MKK7, PRKMK7}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, ZHX2 (zinc fingers and homeoboxes 2) [NCBI Gene 22882] {aka AFR1, RAF}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, CCN2 (cellular communication network factor 2) [NCBI Gene 1490] {aka CTGF, HCS24, IBP-8, IGFBP8, KMD, NOV2}, OCLN (occludin) [NCBI Gene 100506658] {aka BLCPMG, PPP1R115, PTORCH1}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, FFAR3 (free fatty acid receptor 3) [NCBI Gene 2865] {aka FFA3R, GPR41}, TDO2 (tryptophan 2,3-dioxygenase) [NCBI Gene 6999] {aka HYPTRP, TDO, TO, TPH2, TRPO}, SPATA2 (spermatogenesis associated 2) [NCBI Gene 9825] {aka PD1, PPP1R145, tamo}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, AHR (aryl hydrocarbon receptor) [NCBI Gene 196] {aka FVH3, RP85, bHLHe76}, MIR3064 (microRNA 3064) [NCBI Gene 100616387], HMGB1 (high mobility group box 1) [NCBI Gene 3146] {aka HMG-1, HMG1, HMG3, SBP-1}, IGF2BP3 (insulin like growth factor 2 mRNA binding protein 3) [NCBI Gene 10643] {aka CT98, IMP-3, IMP3, KOC, KOC1, VICKZ3}, JUNB (JunB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3726] {aka AP-1}, RXRA (retinoid X receptor alpha) [NCBI Gene 6256] {aka NR2B1, RXR-alpha, RXRalpha}, LINC00665 (long intergenic non-protein coding RNA 665) [NCBI Gene 100506930] {aka CIP2A-BP}, TJP1 (tight junction protein 1) [NCBI Gene 7082] {aka ZO-1}, DLX6-AS1 (DLX6 antisense RNA 1) [NCBI Gene 285987] {aka DLX6-AS, DLX6AS, Evf-2, NCRNA00212, uc.220, uc.221}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, FASN (fatty acid synthase) [NCBI Gene 2194] {aka FAS, OA-519, SDR27X1}, NR1H4 (nuclear receptor subfamily 1 group H member 4) [NCBI Gene 9971] {aka BAR, FXR, HRR-1, HRR1, PFIC5, RIP14}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, TPH1 (tryptophan hydroxylase 1) [NCBI Gene 7166] {aka TPRH, TRPH}, KMO (kynurenine 3-monooxygenase) [NCBI Gene 8564] {aka dJ317G22.1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, HDAC9 (histone deacetylase 9) [NCBI Gene 9734] {aka HD7, HD7b, HD9, HDAC, HDAC7B, HDAC9B}, FFAR2 (free fatty acid receptor 2) [NCBI Gene 2867] {aka FFA2R, GPR43}
- **Diseases:** diarrhea (MESH:D003967), bladder carcinogenesis (MESH:D063646), inflammation (MESH:D007249), BSH (MESH:D013651), melanoma (MESH:D008545), dysbiosis (MESH:D064806), cancer (MESH:D009369), enteritis (MESH:D004751), FMT (MESH:D005242), lung, breast, colorectal, and prostate cancers (MESH:D001943), BC (MESH:D001749), infectious diseases (MESH:D003141), -invasive (MESH:D009361), immune dysregulation (OMIM:614878), tract (MESH:D014570), tumorigenic (MESH:D002471), carcinogenic (MESH:D011230), urothelial carcinoma (MESH:D014523), Clostridium difficile infection (MESH:D003015), metastasis (MESH:D009362), toxicities (MESH:D064420), urinary tract infections (MESH:D014552), MIBC (MESH:D000093284), XL (MESH:D000080345), infection (MESH:D007239), bacteremia (MESH:D016470), colitis (MESH:D003092)
- **Chemicals:** S-adenosylmethionine (MESH:D012436), isoferulic acid (MESH:C008180), kynurenine (MESH:D007737), lipopolysaccharide (MESH:D008070), UDCA (MESH:D014580), steroid (MESH:D013256), serotonin (MESH:D012701), indole (MESH:C030374), SCFA (MESH:D005232), folate (MESH:D005492), acetate (MESH:D000085), gemcitabine (MESH:D000093542), Tryptophan (MESH:D014364), IAA (MESH:C030737), glycosaminoglycans (MESH:D006025), Immune checkpoint (-), cisplatin (MESH:D002945), BAs (MESH:D001647), propionate (MESH:D011422), lithocholic acid (MESH:D008095), N-formylkynurenine (MESH:C007772), butyrate (MESH:D002087)
- **Species:** Parabacteroides distasonis (species) [taxon 823], Brucella (genus) [taxon 234], Veillonella (genus) [taxon 29465], Enterobacterales (order) [taxon 91347], Bacteroides salyersiae (species) [taxon 291644], Eubacterium coprostanoligenes (species) [taxon 290054], Lactobacillus (genus) [taxon 1578], Prevotella (genus) [taxon 838], Mus musculus (house mouse, species) [taxon 10090], Akkermansia (genus) [taxon 239934], Oscillibacter (genus) [taxon 459786], Bacillota (clostridial firmicutes, phylum) [taxon 1239], gut metagenome (species) [taxon 749906], Achromobacter (genus) [taxon 222], Phocaeicola dorei (species) [taxon 357276], Streptococcus (genus) [taxon 1301], Blautia coccoides [taxon 1532], Fusobacteriia (class) [taxon 203490], Clostridium (genus) [taxon 1485], Bifidobacterium (genus) [taxon 1678], Homo sapiens (human, species) [taxon 9606], Fusobacterium (genus) [taxon 848]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12909566/full.md

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Source: https://tomesphere.com/paper/PMC12909566