Evidence map›Paper›PMID 40665305›Full record

ReviewMolecular cancer2025

The tumor microbiome in cancer progression: mechanisms and therapeutic potential.

Wanting Zhang, Yuhang Xiang, He Ren, Yilin Liu, Qi Wang, Mengdi Ran, Wanting Zhou, Lu Tian, Xianhui Zheng, Cong Qiao and 2 more

Abstract readReview
In one paragraph

Review in Molecular cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

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  14. Programming the tumor microenvironment through microbiome-driven mechanisms.Frontiers in cellular and infection microbiology · 2026
    Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. IntratumoralFrontiers in immunology · 2026
    Article
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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

12 authors.

Wanting ZhangDepartment of Pathology, Harbin Medical University, Harbin, 150081, Heilongjiang Province, China.
Yuhang XiangDepartment of Pathology, Harbin Medical University, Harbin, 150081, Heilongjiang Province, China.
He RenDepartment of Oncological Surgery, Harbin Medical University Cancer Hospital, Harbin, 150000, Heilongjiang Province, China.
Yilin LiuDepartment of Oncological Surgery, Harbin Medical University Cancer Hospital, Harbin, 150000, Heilongjiang Province, China.
Qi WangDepartment of Oncological Surgery, Harbin Medical University Cancer Hospital, Harbin, 150000, Heilongjiang Province, China.
Mengdi RanDepartment of Oncological Surgery, Harbin Medical University Cancer Hospital, Harbin, 150000, Heilongjiang Province, China.
Wanting ZhouDepartment of Clinical Laboratory, The First Affiliated Hospital of Dalian Medical University, Dalian, 116011, Liaoning, China.
Lu TianClinical Laboratory, Jiutai People's Hospital, Changchun, 130500, Jilin, China.
Xianhui ZhengSchool of Pharmaceutical Sciences, Shanxi Medical University, Taiyuan, 030600, Shanxi, China.
Cong QiaoDepartment of Pathology, Harbin Medical University, Harbin, 150081, Heilongjiang Province, China.
Yifei LiuSchool of Basic Medical Sciences, Harbin Medical University, Harbin, 150081, Heilongjiang Province, China.
Meisi YanDepartment of Pathology, Harbin Medical University, Harbin, 150081, Heilongjiang Province, China. msyan@hrbmu.edu.cn.

Funding

National Natural Science Foundation of China No.82472867Postgraduate Research & Practice Innovation Program of Harbin Medical University YJSCX2024-78HYDThe Outstanding Young Scholar Project of the Natural Science Foundation of Heilongjiang Province YQ2024H003
6 · The paper itself

Abstract

The tumor microbiome (TM) comprises diverse microbial communities, such as bacteria, fungi, and viruses. Recent advancements in microbial sequencing technologies have improved our understanding of the distribution and functional roles of microbes in solid tumors. The TM is formed through several mechanisms, such as direct invasion of mucosal barriers, diffusion from adjacent normal tissues, metastasis of tumor cells, and dissemination via blood and lymphatic circulation. Microbes play a critical role in the tumor microenvironment (TME), and the TM has a heterogeneous composition in different types of cancer. This heterogeneity affects tumor development, progression, and response to treatment. The TM modulates tumor cell physiology and immune responses via several signaling pathways, such as WNT/β-catenin, NF-κB, toll-like receptors (TLRs), ERK, and stimulator of interferon genes (STING). Extensive studies have characterized the role of TM in tumor progression, revealing the importance of genetic abnormalities, epigenetic changes, metabolic regulation, invasion and metastasis, and chronic inflammatory responses. The role of TM in cancer treatment, especially in immunotherapy, has received increasing attention, demonstrating significant regulatory potential. This review provides an in-depth overview of the development of TM detection technologies, explores its potential origins and heterogeneity, and elucidates the mechanisms by which TM contributes to tumorigenesis or tumor suppression. Furthermore, this review explored how TM can be used in cancer treatment, offering a comprehensive perspective on targeted and personalized approaches.

Indexed as

MicrobiotaNeoplasmsAnimalsDisease ProgressionHumansSignal TransductionTumor MicroenvironmentCancer progressionImmune regulationMicrobial metabolitesTherapeutic interventionsTumor microbiome

Identifiers

PMID40665305
PMCPMC12261620

What OpenQuestion holds

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Registered trials

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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.