Evidence map›Paper›PMID 42830658›Full record

ReviewMicrobiologyOpen2026

The Microbiome in Glioblastoma: Mechanisms, Tumor-Immune Interactions, and Translational Perspectives.

Tareq Nayef AlRamadneh, Renuka Jyothi-S, Priya Priyadarshini-Nayak, Anima Nanda, Shaker Al-Hasnaawei, Akanksha Bhatt, Ashish Singh-Chauhan, Siya Singla, Manoj Kumar Mishra

Abstract readReview
In one paragraph

Review in MicrobiologyOpen, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Tareq Nayef AlRamadnehFaculty of Allied Medical Sciences, Hourani Center for Applied Scientific Research, Al-Ahliyya Amman University, Amman, Jordan.
Renuka Jyothi-SDepartment of Biotechnology and Genetics, School of Sciences, JAIN (Deemed to be University), Bangalore, India.
Priya Priyadarshini-NayakDepartment of Medical Oncology, IMS and SUM Hospital, Siksha 'O' Anusandhan, Bhubaneswar, India.
Anima NandaDepartment of Biomedical, Sathyabama Institute of Science and Technology, Chennai, India.
Shaker Al-HasnaaweiCollege of Pharmacy, The Islamic University, Najaf, Iraq.
Akanksha BhattDepartment of Pharmacy Graphic Era Hill University, Dehradun, India.
Ashish Singh-ChauhanUttaranchal Institute of Pharmaceutical Sciences, Division of Research and Innovation, Uttaranchal University, Dehradun, India.ORCID https://orcid.org/0009-0004-7154-2584
Siya SinglaCenter for Research Impact and Outcome, Chitkara University Institute of Engineering and Technology, Chitkara University, Rajpura, India.
Manoj Kumar MishraIndependent Researcher, Fitche, Ethiopia.ORCID https://orcid.org/0009-0001-4850-2216

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite multimodal treatment, glioblastoma (GBM) remains difficult to control because of diffuse invasion, tumor heterogeneity, immune dysfunction, and frequent recurrence. Increasing attention has focused on whether intestinal microbial communities and their products can modify systemic and central nervous system processes relevant to GBM. This narrative review critically evaluates current evidence linking microbial communities, microbial metabolites, tumor-associated microbial signals, and host immune responses with GBM biology and clinical translation. PubMed, Scopus, Web of Science, and Google Scholar were searched for English-language studies published from January 2019 through August 2026, with earlier foundational studies included when necessary. Human cohorts, tumor-tissue studies, glioma models, microbiota-transfer experiments, and mechanistic investigations were considered. Preclinical evidence supports several plausible pathways, including changes in short-chain fatty acid availability, microglial and macrophage states, blood-brain barrier regulation, systemic immunity, and tryptophan-related signaling. However, many relevant metabolites may originate from microbial, host, immune, or tumor sources. Human studies remain limited and vulnerable to confounding, reverse causation, treatment effects, and geographic variation. Bacterial nucleic acids and bacteria-associated HLA-bound peptides have been detected in brain tumors, but these findings do not establish viable colonization or a gut origin. Low microbial biomass also necessitates rigorous contamination control and orthogonal validation. Microbial influences are biologically plausible modifiers of GBM rather than established drivers. Clinical translation requires longitudinal human studies, source-resolved analyzes, standardized low-biomass methods, mechanistic validation, and independent replication. No microbiome-based biomarker or microbiome-directed therapy is currently validated for routine GBM care or patient stratification in clinical practice.

Indexed as

Brain NeoplasmsGastrointestinal MicrobiomeGlioblastomaMicrobiotaAnimalsHumansTranslational Research, Biomedicalcausal inferenceglioblastomagut microbiotamicrobial metabolitesneuroimmune signalingtranslational readiness

Identifiers

PMID42830658
PMCPMC13635682

What Socratic holds

Textmetadata
Read underepoch 390

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.