Evidence map›Paper›PMID 29686328›Full record

ArticleScientific reports2018

A microfluidic device for studying chemotaxis mechanism of bacterial cancer targeting.

Jing Song, Yu Zhang, Chengqian Zhang, Xiaohui Du, Zhe Guo, Yanbin Kuang, Yingyan Wang, Peng Wu, Kun Zou, Lijuan Zou and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.2field-weighted citation impact, top 9% of its field
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

24 citing papers in PubMed, 67 citations in OpenAlex.

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  18. LncRNAFrontiers in cell and developmental biology · 2022
    Review
  19. Recent advances in bacteria-mediated cancer therapy.Frontiers in bioengineering and biotechnology · 2022
    Review
  20. Article
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

12 authors at 6 institutions in 1 country.

Jing SongDepartment of Respiratory Medicine, The Second Hospital, Dalian Medical University, Dalian, China.
Yu ZhangDepartment of Radiotherapy, The Second Hospital, Dalian Medical University, Dalian, China.
Chengqian ZhangLaboratory of Protein and Peptide Pharmaceuticals and Laboratory of Proteomics, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Xiaohui DuDepartment of Scientific Research Center, The Second Hospital, Dalian Medical University, Dalian, China.
Zhe GuoDepartment of Respiratory Medicine, The Second Hospital, Dalian Medical University, Dalian, China.
Yanbin KuangDepartment of Respiratory Medicine, The Second Hospital, Dalian Medical University, Dalian, China.
Yingyan WangLaboratory Center for Diagnostics, Dalian Medical University, Dalian, China.
Peng WuLaboratory of Protein and Peptide Pharmaceuticals and Laboratory of Proteomics, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Kun ZouDepartment of Radiotherapy, The First Hospital, Dalian Medical University, Dalian, China.
Lijuan ZouDepartment of Radiotherapy, The Second Hospital, Dalian Medical University, Dalian, China. zoulijuan1963@sina.com.
Jianxin LvKey Laboratory of Medical Genetics, Wenzhou Medical University, Wenzhou, China. jxlu313@163.com.
Qi WangDepartment of Respiratory Medicine, The Second Hospital, Dalian Medical University, Dalian, China. wqdlmu@163.com.
Dalian Medical University · CNSecond Affiliated Hospital of Dalian Medical University · CNInstitute of Biophysics · CNFirst Affiliated Hospital of Dalian Medical University · CNFirst Affiliated Hospital of Shantou University Medical College · CNWenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial cancer targeting may become an efficacious cancer therapy, but the mechanisms underlying bacterial specificity for cancer cells need to be explored prior to adopting it as a new clinical application. To characterize the mechanism of bacterial chemotactic preference towards cancer cells, we developed a microfluidic device for in vitro study. The device consists of a cell culture chamber on both sides of a central bacteria channel, with micro-channels used as barriers between them. The device, when used as model for lung cancer, was able to provide simultaneous three-dimensional co-culture of multiple cell lines in separate culture chambers, and when used as model for bacterial chemotaxis, established constant concentration gradients of biochemical compounds in a central channel by diffusion through micro-channels. Fluorescence intensity of green fluorescence protein (GFP)-encoding bacteria was used to measure bacterial taxis behavior due to established chemotactic gradients. Using this platform, we found that Escherichia coli (E. coli) clearly illustrated the preference for lung cancer cells (NCI-H460) which was attributed to biochemical factors secreted by carcinoma cells. Furthermore, by secretome analysis and validation experiments, clusterin (CLU) was found as a key regulator for the chemotaxis of E. coli in targeting lung cancer.

Indexed as

ChemotaxisLab-On-A-Chip DevicesCell Line, TumorCoculture TechniquesEscherichia coli O157Green Fluorescent ProteinsHumansLung NeoplasmsGreen Fluorescent Proteins

Identifiers

PMID29686328
PMCPMC5913277
OpenAlexW2801528548

What OpenQuestion holds

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Registered trials

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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.