Evidence map›Paper›PMID 40792261›Full record

ReviewFrontiers in microbiology2025

Resynthesis of synthetic biology techniques: combining engineered bacteria with other antitumour therapies.

Xueke Chang, Xiaolin Liu, Xiumei Wang, Lin Ma, Jing Liang, Yan Li

Abstract readReview
In one paragraph

Review in Frontiers in microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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

  1. Pooled it
  2. Review
  3. Review
  4. Review
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

6 authors.

Xueke Chang *Department of Oncology, Shandong Provincial Qianfoshan Hospital, Shandong Lung Cancer Institute, The First Affiliated Hospital of Shandong First Medical University, Jinan, China.
Xiaolin Liu *Department of Oncology, Shandong Provincial Qianfoshan Hospital, Shandong Lung Cancer Institute, The First Affiliated Hospital of Shandong First Medical University, Jinan, China.
Xiumei Wang *Yuncheng Chengxin Hospital, Heze, Shandong, China.
Lin MaDepartment of Oncology, Shandong Provincial Qianfoshan Hospital, Shandong Lung Cancer Institute, The First Affiliated Hospital of Shandong First Medical University, Jinan, China.
Jing Liang *Department of Oncology, Shandong Provincial Qianfoshan Hospital, Shandong Lung Cancer Institute, The First Affiliated Hospital of Shandong First Medical University, Jinan, China.
Yan Li *Department of Oncology, Shandong Provincial Qianfoshan Hospital, Shandong Lung Cancer Institute, The First Affiliated Hospital of Shandong First Medical University, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Worldwide cancer mortality rates underscore the pressing need to identify and develop novel anticancer therapies to supplement traditional cancer treatments. Naturally occurring bacteria are ideal for cancer therapy owing to their autonomous propulsion and hypoxia-targeting properties, but their poor tumour targeting ability and weak tumour penetration limit their use. Bacteria can be modified by bioengineering and nanotechnology methods to improve their physiological activity and therapeutic effect. Furthermore, engineering allows for refined spatiotemporal control, precise functional recombination, and direct genetic reprogramming. These engineered bacteria can produce synergistic anticancer effects upon coadministration with anticancer drug-containing nanomaterials or other therapeutic payloads. In this paper, the use of engineered bacteria combined with other antitumour therapies, such as radiotherapy (RT), chemotherapy, immunotherapy, light therapy and life technology, is reviewed to aid in improving antitumour therapy efficacy. In addition, we provide an overview of the current state of spatiotemporally regulated bacterial gene expression and drug release, discuss the drawbacks and difficulties of employing engineered bacteria for tumour therapy, and explore potential research avenues on the basis of current advancements.

Indexed as

antitumour therapyengineered bacteriaspatiotemporal manipulationsynthetic biologytherapeutic effect

Identifiers

PMID40792261
PMCPMC12336869

What OpenQuestion holds

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LicenceCC BY
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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.