Evidence map›Paper›PMID 31827064›Full record

ReviewExperimental & molecular medicine2019

Bacteria-cancer interactions: bacteria-based cancer therapy.

Mai Thi-Quynh Duong, Yeshan Qin, Sung-Hwan You, Jung-Joon Min

Abstract readReview
In one paragraph

Review in Experimental & molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 237 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
237citing papers in PubMed, 2 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

237 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Myokines and mitochondrial function in cardiometabolic diseases.Journal of physiology and biochemistry · 2026
    Review
  6. Review
  7. Review
  8. Article
  9. Engineered probioticScience advances · 2026
    Article
  10. Living Microbial Drugs.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026
    Review
  11. Review
  12. EngineeredMolecular therapy. Oncology · 2026
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Review

177 more citing papers are in PubMed but not listed here.

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

4 authors.

Mai Thi-Quynh DuongLaboratory of In vivo Molecular Imaging, Institute for Molecular Imaging and Theranostics, Chonnam National University Medical School and Hwasun Hospital, Jeonnam, 58128, Republic of Korea.
Yeshan QinLaboratory of In vivo Molecular Imaging, Institute for Molecular Imaging and Theranostics, Chonnam National University Medical School and Hwasun Hospital, Jeonnam, 58128, Republic of Korea.
Sung-Hwan YouLaboratory of In vivo Molecular Imaging, Institute for Molecular Imaging and Theranostics, Chonnam National University Medical School and Hwasun Hospital, Jeonnam, 58128, Republic of Korea.
Jung-Joon MinLaboratory of In vivo Molecular Imaging, Institute for Molecular Imaging and Theranostics, Chonnam National University Medical School and Hwasun Hospital, Jeonnam, 58128, Republic of Korea. jjmin@jnu.ac.kr.

Funding

National Research Foundation of Korea (NRF) NRF-2017R1A2B3012157
6 · The paper itself

Abstract

Recent advances in cancer therapeutics, such as targeted therapy and immunotherapy, have raised the hope for cures for many cancer types. However, there are still ongoing challenges to the pursuit of novel therapeutic approaches, including high toxicity to normal tissue and cells, difficulties in treating deep tumor tissue, and the possibility of drug resistance in tumor cells. The use of live tumor-targeting bacteria provides a unique therapeutic option that meets these challenges. Compared with most other therapeutics, tumor-targeting bacteria have versatile capabilities for suppressing cancer. Bacteria preferentially accumulate and proliferate within tumors, where they can initiate antitumor immune responses. Bacteria can be further programmed via simple genetic manipulation or sophisticated synthetic bioengineering to produce and deliver anticancer agents based on clinical needs. Therapeutic approaches using live tumor-targeting bacteria can be applied either as a monotherapy or in combination with other anticancer therapies to achieve better clinical outcomes. In this review, we introduce and summarize the potential benefits and challenges of this anticancer approach. We further discuss how live bacteria interact with tumor microenvironments to induce tumor regression. We also provide examples of different methods for engineering bacteria to improve efficacy and safety. Finally, we introduce past and ongoing clinical trials involving tumor-targeting bacteria.

Indexed as

Antineoplastic AgentsBacteriaHumansImmunotherapyNeoplasmsTumor MicroenvironmentAntineoplastic Agents

Identifiers

PMID31827064
PMCPMC6906302

What OpenQuestion holds

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LicenceCC BY
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 OpenQuestion graph.