Evidence map›Paper›PMID 31145345›Full record

ArticleMedicine2019

Interleukin-24 enhancing antitumor activity of chimeric oncolytic adenovirus for treating acute promyelocytic leukemia cell.

Li Liu, Jiabin Ma, Lanyi Qin, Xiaogang Shi, Hongqiang Si, Yahui Wei

Abstract read
In one paragraph

Article in Medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Role of Adenoviruses in Cancer Therapy.Frontiers in oncology · 2022
    Review
  3. Article
  4. Review
  5. Review
  6. 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

6 authors.

Li LiuKey Laboratory of Resource Biology and Biotechnology in Western China, Department of Life Science, Northwest University, Xi'an, Shannxi.
Jiabin MaSchool of Life Sciences, Zhejiang Sci-Tech University, Hangzhou, Zhejiang, P.R. China.
Lanyi QinSchool of Life Sciences, Zhejiang Sci-Tech University, Hangzhou, Zhejiang, P.R. China.
Xiaogang ShiSchool of Life Sciences, Zhejiang Sci-Tech University, Hangzhou, Zhejiang, P.R. China.
Hongqiang SiSchool of Life Sciences, Zhejiang Sci-Tech University, Hangzhou, Zhejiang, P.R. China.
Yahui WeiKey Laboratory of Resource Biology and Biotechnology in Western China, Department of Life Science, Northwest University, Xi'an, Shannxi.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute promyelocytic leukaemia (APL) is a clonal disease arising by hematopoietic stem cell (HSC), which characterized by inappropriate proliferation/differentiation or survival of immature myeloid progenitors. Oncolytic adenoviruses have been under widespread investigation as anticancer agents. Recently, our data suggested that tumor cells were cured by AdCN205-IL-24, an adenovirus serotype 5-based conditionally replicating adenovirus expressing IL-24 after infection.

methodsIn this study, we created a novel fiber chimeric oncolytic adenovirus AdCN306-IL-24 that has Ad11 tropism and approved CAR (coxsackie adenovirus receptor, CAR)-independent cell entry, which could allow development of selective cytopathic effects (CPE) in APL cells in vitro.

resultsFormidable cytotoxic effect was specifically implemented in APL cells after infection with AdCN306-IL-24. The expression of IL-24 was up-regulated upon treated with accepted tumors. And the vector also induced superior cytolytic effects activity in APL cells by activation of programmed cell death.

conclusionsTaken together, our data suggested that chimeric oncolytic adenovirus AdCN306-IL-24 could express IL-24 gene, representing a potential therapeutics for acute promyelocytic leukemia.

Indexed as

Adenovirus Early ProteinsChimeraHEK293 CellsHL-60 CellsHumansInterleukin-24InterleukinsLeukemia, Promyelocytic, AcuteOncolytic VirotherapyOncolytic VirusesAdenovirus Early ProteinsInterleukin-24Interleukins

Identifiers

PMID31145345
PMCPMC6708966

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.