# The Role of the Oral Microbiome in Modulating Therapeutic Outcomes in Lung Cancer: Key Commensals and Clinical Implications

**Authors:** Tiara Hening Pertiwi, Ratoe Suraya, Masaya Akashi, Tatsuya Nagano

PMC · DOI: 10.3390/cancers18040591 · Cancers · 2026-02-11

## TL;DR

This review explores how the oral microbiome influences lung cancer treatment outcomes and highlights the need for further research on microbiome-targeting interventions.

## Contribution

The paper provides a comprehensive review of the oral microbiome's role in lung cancer therapy and its modulation as a potential treatment strategy.

## Key findings

- Oral microbiome dysbiosis is linked to lung cancer development and treatment outcomes.
- Interventions targeting the oral microbiome show promise in improving lung cancer treatment efficacy.
- More large-scale studies are needed to validate these interventions and maximize their effectiveness.

## Abstract

Due to a variety of underlying factors, the oral microbiome is a sometimes disregarded yet unquestionably significant factor that can change the course and overall outcome of lung cancer therapy. In recent years, dysbiosis in the oral microbiome has been correlated not only with the occurrence of lung cancer but also with its treatment outcome. Accordingly, several intervention strategies, such as probiotics, antimicrobial peptides, and oral hygiene care, have been developed to combat oral dysbiosis in lung cancer conditions with varying levels of success; more research is necessary to validate these strategies as a supplement to the available lung cancer treatments and maximize their effectiveness.

Lung cancer remains one of the deadliest forms of cancer worldwide; thus, there is an urgent need to continually devise new strategies to effectively treat this condition. In this review, we will discuss one of the previously less studied but important aspects of the oral microbiome in both accelerating the development of lung cancer and modulating the efficacy of its treatment modalities. Herein, following an exhaustive search of available databases, we summarize the current knowledge on the association between oral microbiota and lung cancer, focusing on its impact on the efficacy and complications of widely used lung cancer treatments, including surgery, radiotherapy, chemotherapy, and immunotherapy. We also discuss the evidence supporting the use of oral microbiome-targeting interventions in improving outcomes in lung cancer, both preclinically and clinically, and conclude that the full potential of modulating oral dysbiosis in lung cancer has yet to be realized, requiring broader and larger-scale studies in the future. We hope that this review will highlight the importance of an often-forgotten aspect of lung cancer treatment optimization.

## Linked entities

- **Diseases:** lung cancer (MONDO:0005138)

## Full-text entities

- **Genes:** FOS (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2353] {aka AP-1, C-FOS, p55}, JUN (Jun proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 3725] {aka AP-1, AP1, c-Jun, cJUN, p39}, PCDHB13 (protocadherin beta 13) [NCBI Gene 56123] {aka PCDH-BETA13}, FOSB (FosB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2354] {aka AP-1, G0S3, GOS3, GOSB}, TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, CAMP (cathelicidin antimicrobial peptide) [NCBI Gene 820] {aka CAP-18, CAP18, CRAMP, FALL-39, FALL39, HSD26}
- **Diseases:** periodontal infections (MESH:D010518), Chronic inflammation (MESH:D007249), pulmonary infections (MESH:D012141), injury to (MESH:D014947), small cell lung cancer (MESH:D055752), Cancer (MESH:D009369), Oral Dysbiosis (MESH:D064806), Lung Cancer (MESH:D008175), febrile (MESH:D000071072), gastric cancer (MESH:D013274), respiratory and oral disorders (MESH:D012131), pneumonia (MESH:D011014), carcinogenesis (MESH:D063646), diarrhea (MESH:D003967), hematopoietic malignancy (MESH:D019337), NSCLC (MESH:D002289), anemia (MESH:D000740), colon cancer (MESH:D015179), deaths (MESH:D003643), neutropenia (MESH:D009503), carcinogenic (MESH:D011230), dental complications (MESH:D009057), infections (MESH:D007239), pulmonary health (OMIM:603663), oral mucositis (MESH:D013280), cytotoxicity (MESH:D064420), aspiration pneumonia (MESH:D011015), gastrointestinal cancers (MESH:D005770), aphthous ulceration (MESH:D013281)
- **Chemicals:** platinum (MESH:D010984), oxygen (MESH:D010100), AMP (MESH:D000089882), paclitaxel (MESH:D017239), methotrexate (MESH:D008727), atezolizumab (MESH:C000594389), Peptides (MESH:D010455), vinorelbine (MESH:D000077235), bevacizumab (MESH:D000068258), pemetrexed (MESH:D000068437), BP-1 (-), hydrogen peroxide (MESH:D006861), doxorubicin (MESH:D004317), taxanes (MESH:D043823), alcohol (MESH:D000438), gemcitabine (MESH:D000093542), calcium (MESH:D002118)
- **Species:** Candida albicans (species) [taxon 5476], Aggregatibacter actinomycetemcomitans (species) [taxon 714], Lacticaseibacillus rhamnosus GG (strain) [taxon 568703], Porphyromonas endodontalis (species) [taxon 28124], Haemophilus (genus) [taxon 724], Streptococcus sanguinis (species) [taxon 1305], Neisseria (genus) [taxon 482], Rothia aeria (species) [taxon 172042], Actinomyces (genus) [taxon 1654], Sphingomonas (genus) [taxon 13687], Lactococcus lactis (species) [taxon 1358], Clostridium butyricum (species) [taxon 1492], Streptococcus pyogenes (species) [taxon 1314], Aeromonas (genus) [taxon 642], Nicotiana tabacum (American tobacco, species) [taxon 4097], Legionella (genus) [taxon 445], Oreochromis niloticus (Nile tilapia, species) [taxon 8128], Lacticaseibacillus casei (species) [taxon 1582], Rothia (genus) [taxon 508215], Lactobacillus acidophilus NCFM (strain) [taxon 272621], Staphylococcus (genus) [taxon 1279], Segatella salivae (species) [taxon 228604], Homo sapiens (human, species) [taxon 9606], Lacticaseibacillus rhamnosus HN001 (strain) [taxon 486408], Fusobacterium nucleatum (species) [taxon 851]
- **Cell lines:** A549 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023)

## Full text

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## Figures

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## References

75 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938800/full.md

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Source: https://tomesphere.com/paper/PMC12938800