Evidence map›Paper›PMID 40764397›Full record

ArticleNature biomedical engineering2026

Tumour-resident oncolytic bacteria trigger potent anticancer effects through selective intratumoural thrombosis and necrosis.

Seigo Iwata, Taisei Nishiyama, Matomo Sakari, Yuki Doi, Naoki Takaya, Yusuke Ogitani, Hiroshi Nagano, Keisuke Fukuchi, Eijiro Miyako

Abstract read
In one paragraph

Article in Nature biomedical engineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  13. 2025 in review.Nature biomedical engineering · 2025
    Article
  14. Systemic administration ofJournal for immunotherapy of cancer · 2025
    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

9 authors.

Seigo IwataGraduate School of Advanced Science and Technology, Japan Advanced Institute of Science and Technology, Nomi, Japan.
Taisei NishiyamaGraduate School of Advanced Science and Technology, Japan Advanced Institute of Science and Technology, Nomi, Japan.
Matomo SakariGraduate School of Advanced Science and Technology, Japan Advanced Institute of Science and Technology, Nomi, Japan.
Yuki DoiFaculty of Life and Environmental Sciences, Microbiology Research Center for Sustainability, University of Tsukuba, Tsukuba, Japan.
Naoki TakayaFaculty of Life and Environmental Sciences, Microbiology Research Center for Sustainability, University of Tsukuba, Tsukuba, Japan.
Yusuke OgitaniDiscovery Research Laboratories I, Research Function, R&D Division, Daiichi Sankyo Co., Ltd, Shinagawa, Japan.
Hiroshi NaganoDiscovery Research Laboratories I, Research Function, R&D Division, Daiichi Sankyo Co., Ltd, Shinagawa, Japan.
Keisuke FukuchiDiscovery Research Laboratories I, Research Function, R&D Division, Daiichi Sankyo Co., Ltd, Shinagawa, Japan.
Eijiro MiyakoGraduate School of Advanced Science and Technology, Japan Advanced Institute of Science and Technology, Nomi, Japan. e-miyako@jaist.ac.jp.ORCID http://orcid.org/0000-0002-1157-6174

Funding

Daiichi Sankyo Company (Sankyo Company) N.A.Institute for Fermentation, Osaka (IFO) N.A.MEXT | Japan Science and Technology Agency (JST) JPMJSF2318MEXT | Japan Science and Technology Agency (JST) JPMJSP2102MEXT | Japan Science and Technology Agency (JST) JPMJTR22U1MEXT | Japan Society for the Promotion of Science (JSPS) 22K18440MEXT | Japan Society for the Promotion of Science (JSPS) 23H00551Uehara Memorial Foundation N.A.
6 · The paper itself

Abstract

Intratumoural bacteria represent a promising drug-free strategy in cancer therapy. Here we demonstrate that a tumour-resident bacterial consortium-Proteus mirabilis (A-gyo) and Rhodopseudomonas palustris (UN-gyo)-in a precise 3:97 ratio (A-gyo:UN-gyo), exhibits potent antitumour efficacy independent of immune cell infiltration. In both immunocompetent and immunocompromised mouse models, including human tumour xenografts, intravenous administration of the bacterial consortium led to complete tumour remission, prolonged survival, and no observable systemic toxicity or cytokine release syndrome. Genomic and phenotypic analyses revealed A-gyo's unique non-pathogenic profile and impaired motility, while UN-gyo modulated A-gyo's biogenic activity, enhanced safety and promoted cancer-specific transformation. Mechanistically, the bacterial consortium triggered selective intratumoural thrombosis and vascular collapse-supported by cytokine induction, fibrin deposition and platelet aggregation-culminating in widespread tumour necrosis. The consortium also proliferated within tumours, formed biofilms and exerted direct oncolytic effects. This natural bacterial synergy-achieved without genetic engineering-offers a self-regulating and controllable strategy for safe, tumour-targeted therapy.

Indexed as

NeoplasmsThrombosisAnimalsCell Line, TumorCytokinesFemaleHumansMiceNecrosisXenograft Model Antitumor AssaysCytokines

Identifiers

PMID40764397
PMCPMC12920090

What OpenQuestion holds

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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 OpenQuestion graph.