ReviewMedComm2026
Intratumoral Microbiota in Fueling Cancer and Steering Treatment Response.
Review in MedComm, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Microorganisms within tumors, also known as intratumoral microbiota, actively shape the tumor microenvironment (TME), influencing cancer progression and treatment response. Research has therefore expanded beyond the gut microbiota to intratumoral bacterial and fungal communities. Advances in low-biomass sequencing, contamination control, and spatial profiling have made it possible to detect these low-abundance microbes within the TME and map their marked heterogeneity across cancer types and tissue compartments. However, their origins, causal functions, and clinical relevance remain debated. Here, we summarize contamination-sensitive workflows and high-resolution techniques required for low-biomass tissues, and compare representative taxa in major cancer settings. We further explore microbial origins, taxonomic diversity, and localized interactions with malignant, immune, and stromal cells. We synthesize mechanistic evidence linking intratumoral microbes to genomic instability, epigenetic regulation, oncogenic signaling, metabolic reprogramming, and metastasis. Based on these insights, we evaluate their impact on cancer therapies, alongside emerging microbial interventions and barriers to clinical translation. Ultimately, this review provides a framework for assessing intratumoral microbiota as biomarkers, treatment-response modifiers, and therapeutic targets, while highlighting the key evidence needed to translate these findings into the clinic.
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Registered trials
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 OpenQuestion graph.