Evidence map›Paper›PMID 42557624›Full record

ArticleAdvanced healthcare materials2026

An Engineered Bacterial Platform Combining Photothermal Ablation with Immunogenic Cell Death and Microenvironment Remodeling for Synergistic Tumor Therapy.

Pandi Peng, Peiren Wang, Xue Yang, Luofeng Yu, Jinxi Liu, Tao Feng, Peng Li

Abstract read
In one paragraph

Article in Advanced healthcare materials, 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

7 authors.

Pandi PengState Key Laboratory of Flexible Electronics (LoFE), Xi'an Institute of Flexible Electronics, and Xi'an Institute of Biomedical Materials and Engineering, Northwestern Polytechnical University, Xi'an, China.
Peiren WangState Key Laboratory of Flexible Electronics (LoFE), Xi'an Institute of Flexible Electronics, and Xi'an Institute of Biomedical Materials and Engineering, Northwestern Polytechnical University, Xi'an, China.
Xue YangState Key Laboratory of Flexible Electronics (LoFE), Xi'an Institute of Flexible Electronics, and Xi'an Institute of Biomedical Materials and Engineering, Northwestern Polytechnical University, Xi'an, China.
Luofeng YuState Key Laboratory of Flexible Electronics (LoFE), Xi'an Institute of Flexible Electronics, and Xi'an Institute of Biomedical Materials and Engineering, Northwestern Polytechnical University, Xi'an, China.ORCID https://orcid.org/0000-0003-2695-1800
Jinxi LiuState Key Laboratory of Flexible Electronics (LoFE), Xi'an Institute of Flexible Electronics, and Xi'an Institute of Biomedical Materials and Engineering, Northwestern Polytechnical University, Xi'an, China.
Tao FengState Key Laboratory of Flexible Electronics (LoFE), Xi'an Institute of Flexible Electronics, and Xi'an Institute of Biomedical Materials and Engineering, Northwestern Polytechnical University, Xi'an, China.
Peng LiState Key Laboratory of Flexible Electronics (LoFE), Xi'an Institute of Flexible Electronics, and Xi'an Institute of Biomedical Materials and Engineering, Northwestern Polytechnical University, Xi'an, China.ORCID https://orcid.org/0000-0002-5876-2177

Funding

Fundamental Research Funds for the Central UniversitiesNational Natural Science Foundation of China 52003222National Natural Science Foundation of China 52473265Shaanxi Provincial Science Fund for Distinguished Young Scholars 2023-JC-JQ-32
6 · The paper itself

Abstract

Cancer poses a significant burden on human health and has emerged as a pressing global public health issue. Conventional cancer therapies are constrained by poor spatial precision in drug delivery, inadequate immunogenic cell death, and persistence of immunosuppressive M2-like tumor-associated macrophages. These limitations perpetuate off-target toxicity, immune evasion, and tumor recurrence. In this study, we engineered an integrated therapeutic platform, HA/IR780@Bac, through leveraging hypoxia-responsive Escherichia coli to co-deliver immunomodulating hyaluronic acid (HA) and the photothermal agent IR780 for synergistic cancer eradication. The system exploited bacterial tropism to achieve tumor-targeted accumulation, and mediated localized photothermal ablation of tumor cells while concurrently triggered robust immunogenic cell death. This immunogenic cell death cascade-initiated cancer immunogenicity and reversed immunosuppression, which was further amplified by HA-driven polarization of tumor-associated macrophages from pro-tumoral M2 to antitumoral M1 phenotype. Therefore, the HA/IR780@Bac system, which combined targeted delivery, photothermal effect, immunogenic cell death activation, and macrophage reprogramming, could establish a robust paradigm for synergistic tumor treatment.

Indexed as

Escherichia coliImmunogenic Cell DeathNeoplasmsPhotothermal TherapyTumor MicroenvironmentAnimalsCell Line, TumorFemaleHumansHyaluronic AcidIndolesMiceHyaluronic AcidIndolesimmunogenic cell deathmacrophage polarizationphotothermal therapysynergistic therapytumor‐targeting bacteria

Identifiers

PMID42557624
PMCPMC13568896

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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.