Evidence map›Paper›PMID 38708180›Full record

ArticleInternational journal of nanomedicine2024

Nanoparticle/Engineered Bacteria Based Triple-Strategy Delivery System for Enhanced Hepatocellular Carcinoma Cancer Therapy.

Meiyang Yang, Weijun Chen, Dhanu Gupta, Congjin Mei, Yang Yang, Bingke Zhao, Lipeng Qiu, Jinghua Chen

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
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  3. Fever Inspiration: Precision Engineering for Safe and Systemic Immunotherapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  4. Review
  5. Review
  6. 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

8 authors.

Meiyang Yang *School of Life Sciences and Health Engineering, Jiangnan University, Wuxi, People's Republic of China.
Weijun Chen *School of Life Sciences and Health Engineering, Jiangnan University, Wuxi, People's Republic of China.
Dhanu GuptaDepartment of Paediatrics, University of Oxford, Oxford, UK.
Congjin MeiSchool of Life Sciences and Health Engineering, Jiangnan University, Wuxi, People's Republic of China.
Yang YangSchool of Life Sciences and Health Engineering, Jiangnan University, Wuxi, People's Republic of China.
Bingke ZhaoSchool of Life Sciences and Health Engineering, Jiangnan University, Wuxi, People's Republic of China.
Lipeng QiuSchool of Life Sciences and Health Engineering, Jiangnan University, Wuxi, People's Republic of China.
Jinghua ChenSchool of Life Sciences and Health Engineering, Jiangnan University, Wuxi, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: New treatment modalities for hepatocellular carcinoma (HCC) are desperately critically needed, given the lack of specificity, severe side effects, and drug resistance with single chemotherapy. Engineered bacteria can target and accumulate in tumor tissues, induce an immune response, and act as drug delivery vehicles. However, conventional bacterial therapy has limitations, such as drug loading capacity and difficult cargo release, resulting in inadequate therapeutic outcomes. Synthetic biotechnology can enhance the precision and efficacy of bacteria-based delivery systems. This enables the selective release of therapeutic payloads in vivo. Methods: In this study, we constructed a non-pathogenic Results: The results demonstrated that upon intravenous injection into tumor-bearing mice, ASEc can actively target and colonise tumor sites. The lytic genes to achieve blast and concentrated release of Ag significantly increased cytokine secretion and the intratumoral infiltration of CD4/CD8 Conclusion: The novel drug delivery system significantly suppressed HCC in vivo with reduced side effects, indicating a potential strategy for clinical HCC therapy.

Indexed as

Carcinoma, HepatocellularDoxorubicinEscherichia coliLiver NeoplasmsAnimalsDrug Delivery SystemsHepatitis B Surface AntigensHep G2 CellsHumansMiceMice, Inbred BALB CNanoparticlesSulfotransferasesXenograft Model Antitumor AssaysDoxorubicinHepatitis B Surface AntigensSulfotransferasesanti-angiogenesischemotherapyengineered bacteriahepatocellular carcinomaimmunotherapy

Identifiers

PMID38708180
PMCPMC11068060

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.