Evidence map›Paper›PMID 39209449›Full record

ArticleJournal for immunotherapy of cancer2024

Adenovirus vaccine targeting kinases induces potent antitumor immunity in solid tumors.

Fei Zhu, Zheng Lu, Wenjing Tang, Guangya Zhao, Yingxiang Shao, Bowen Lu, Jiage Ding, Yanyan Zheng, Lin Fang, Huizhong Li and 4 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

14 authors.

Fei Zhu *Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Zheng Lu *Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Wenjing TangClinical Laboratory, The Affiliated Huai'an Hospital of Xuzhou Medical University and Huai'an Second Hospital, Huai'an, Jiangsu, China.
Guangya ZhaoCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Yingxiang ShaoCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Bowen LuCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Jiage DingDepartment of Oncology, Xuzhou Central Hospital, Xuzhou Clinical School of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Yanyan ZhengCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Lin FangCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Huizhong LiCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Gang WangCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.ORCID http://orcid.org/0000-0001-6020-7263
Renjin ChenCollege of Life Sciences, Xuzhou Medical University, Xuzhou, Jiangsu, China chaidafei@xzhmu.edu.cn jnzheng@xzhmu.edu.cn crj@xzhmu.edu.cn.
Junnian ZhengCenter of Clinical Oncology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China chaidafei@xzhmu.edu.cn jnzheng@xzhmu.edu.cn crj@xzhmu.edu.cn.ORCID http://orcid.org/0000-0003-0208-6410
Dafei ChaiCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China chaidafei@xzhmu.edu.cn jnzheng@xzhmu.edu.cn crj@xzhmu.edu.cn.ORCID http://orcid.org/0000-0002-8028-2954

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTargeting kinases presents a potential strategy for treating solid tumors; however, the therapeutic potential of vaccines targeting kinases remains uncertain.

methodsAdenovirus (Ad) vaccines encoding Aurora kinase A (AURKA) or cyclin-dependent kinase 7 (CDK7) were developed, and their therapeutic potentials were investigated by various methods including western blot, flow cytometry, cytotoxic T lymphocyte assay, and enzyme-linked immunospot (ELISpot), in mouse and humanized solid tumor models.

resultsCo-immunization with Ad-AURKA/CDK7 effectively prevented subcutaneous tumor growth in the Renca, RM-1, MC38, and Hepa1-6 tumor models. In therapeutic tumor models, Ad-AURKA/CDK7 treatment impeded tumor growth and increased immune cell infiltration. Administration of Ad-AURKA/CDK7 promoted the induction and maturation of dendritic cell subsets and augmented multifunctional CD8

conclusionsOur findings illustrate that the Ad-AURKA/CDK7 vaccine targeting dual kinases AURKA and CDK7 emerges as a promising and effective therapeutic approach for the treatment of solid tumors.

Indexed as

Aurora Kinase ACancer VaccinesAdenoviridaeAdenovirus VaccinesAnimalsCD8-Positive T-LymphocytesCell Line, TumorCyclin-Dependent Kinase-Activating KinaseFemaleHumansMiceNeoplasmsAdenovirus VaccinesAurora Kinase ACancer VaccinesCyclin-Dependent Kinase-Activating KinaseDendriticImmunotherapySolid tumorT cellVaccine

Identifiers

PMID39209449
PMCPMC11367354

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.