Evidence map›Paper›PMID 39482550›Full record

ArticleMolecular biomedicine2024

Decorin-armed oncolytic adenovirus promotes natural killers (NKs) activation and infiltration to enhance NK therapy in CRC model.

Xue Li, Yuning Zhang, Zhuang Mao, Huiqiang Zhao, Hu Cao, Jingyi Wang, Wei Liu, Shiyun Dai, Yuefeng Yang, Yuanyuan Huang and 1 more

Abstract read
In one paragraph

Article in Molecular biomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Trial
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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

11 authors.

Xue Li *College of Life Science, Anhui Medical University, Hefei, 230032, P.R. China.
Yuning Zhang *Department of Oncology, The Fifth Medical Center, Chinese PLA General Hospital, Beijing, 100071, China.
Zhuang MaoBeijing Institute of Radiation Medicine, Beijing, 100850, China.
Huiqiang ZhaoDepartment of Healthcare, The Second Medical Center & National Clinical Research Center for Geriatric Diseases, Chinese PLA General Hospital, Beijing, 100853, China.
Hu CaoBeijing Institute of Radiation Medicine, Beijing, 100850, China.
Jingyi WangBeijing Jingda Biotechnology Co. Ltd, Beijing, 102629, China.
Wei LiuBeijing Jingda Biotechnology Co. Ltd, Beijing, 102629, China.
Shiyun DaiBeijing Jingda Biotechnology Co. Ltd, Beijing, 102629, China.
Yuefeng YangDepartment of Experimental Medical Science, Ningbo No.2 Hospital, Ningbo, 315010, China.
Yuanyuan HuangBeijing Jingda Biotechnology Co. Ltd, Beijing, 102629, China. huangyy@jingdabio.com.
Hua WangCollege of Life Science, Anhui Medical University, Hefei, 230032, P.R. China. 18511712135@163.com.ORCID 0000-0002-5728-7714

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is a prevalent malignant tumor of the gastrointestinal system, with the third and second highest incidence and mortality rates globally in 2020, respectively. Immunotherapy has developed rapidly in recent years. Natural killer (NK) cells have received increasing attention in the field of tumor immunotherapy due to their recognition and killing tumor cells without the limitations of major histocompatibility complexes. However, constraints within the tumor microenvironment that impede the infiltration and proliferation of NK cells result in poor efficacy of NK cell therapy for solid tumors. Oncolytic viral therapy is an immunogenic treatment with the potential to enhance anti-tumour immune responses and promote immune cell infiltration. In this study, we synergistically combine NK cells with an oncolytic adenovirus carrying Decorin (rAd.DCN) for the treatment of colorectal cancer (CRC) in a xenograft mouse model. By using Flow cytometry, real-time quantitative PCR and Calcein-AM release assay, we found that rAd.DCN could effectively promote proliferation, activation and degranulation of NK cells, up-regulate expression and secretion of NK cell killing activity-related factors, and enhance their killing activity. The efficacy is better than that of the blank control oncolytic virus rAd.Null. Combined treatment significantly inhibited tumor growth, increased the number of NK cells in peripheral blood, promoted the killing function of NK cells, and increased the expression levels of perforin and IFN-γ. At the same time, more NK cells were recruited to infiltrate tumor tissue. Our study established the feasibility of combination NK cells and oncolytic adenovirus application, thus expanding the scope of potentially curative treatments for NK cells in CRC.

Indexed as

AdenoviridaeColorectal NeoplasmsDecorinKiller Cells, NaturalOncolytic VirotherapyOncolytic VirusesAnimalsCell Line, TumorCell ProliferationFemaleHumansLymphocyte ActivationMiceTumor MicroenvironmentXenograft Model Antitumor AssaysDecorinAdoptive NK cell therapyColorectal cancerDecorinOncolytic adenovirus

Identifiers

PMID39482550
PMCPMC11527862

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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.