Evidence map›Paper›PMID 33274495›Full record

ArticleJournal of clinical laboratory analysis2021

Luteolin enhances the antitumor efficacy of oncolytic vaccinia virus that harbors IL-24 gene in liver cancer cells.

Chunming Wang, Qiang Li, Boduan Xiao, Huiling Fang, Biao Huang, Fang Huang, Yigang Wang

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

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  18. Frontiers in pharmacology · 2022
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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

7 authors at 2 institutions in 1 country.

Chunming WangCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.ORCID https://orcid.org/0000-0001-6534-7302
Qiang LiCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.
Boduan XiaoCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.
Huiling FangCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.
Biao HuangCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.
Fang HuangDepartment of Pathology, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, China.
Yigang WangCollege of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.
Zhejiang Sci-Tech University · CNZhejiang Provincial People's Hospital · CN

Funding

- -- 18042291- YNational Natural Science Foundation of China 81803069Natural Science Foundation of Zhejiang Province of China LY18C070002Science Foundation of Zhejiang Sci -Science Foundation of Zhejiang Sci 18042291Science Foundation of Zhejiang Sci YTech University (ZSTU) -Tech University (ZSTU) 18042291Tech University (ZSTU) Y
6 · The paper itself

Abstract

backgroundInterleukin 24 (IL-24) is an IL-10 family member and a secreted cytokine characterized by cancer-targeted toxicity and can activate apoptosis by sensitizing cancer cells to chemotherapy. Cytotoxic effects of luteolin on different types of cancer cells suppress their growth by acting on the components of the apoptosis signaling cascade. Therefore, our study aimed to prove whether oncolytic vaccinia virus (VV) that harbors IL-24 (VV-IL-24) combine with luteolin exerts a synergistic inhibitory effect in liver cancer cells.

methodsImpacts on cell viability of VV-IL-24 and luteolin were assessed by MTT in various liver cancer cell lines. Then, liver cancer cell apoptosis was analyzed via flow cytometry and Western blotting. Besides, the MHCC97-H xenograft mouse model was employed as a means of assessing in vivo antitumor efficacy.

resultsMTT assay confirmed that the combination treatment decreased liver cancer cells viability to a greater degree than treatment with VV-IL-24 or luteolin alone. Flow cytometry and Western blot assay proved that VV-IL-24 plus luteolin induced more liver cancer cells apoptosis than single treatment. Furthermore, in the MHCC97-H xenograft model, 15 days of treatment with VV-IL-24 plus luteolin inhibited tumor growth significantly more than single treatment.

conclusionThese data confirm that the synergistic mechanism of VV-IL-24 and luteolin elicits a stronger tumor growth inhibition than any single therapy. Thus, the combination of VV-IL-24 and luteolin could provide the basis for preclinical research in the treatment of liver cancer.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell Line, TumorCell SurvivalFemaleHumansInterleukin-24InterleukinsLiver NeoplasmsLuteolinMiceMice, Inbred BALB COncolytic VirotherapyOncolytic VirusesVaccinia virusAntineoplastic AgentsInterleukin-24InterleukinsLuteolinIL-24 geneliver cancerluteolinoncolytic vaccinia virus

Identifiers

PMID33274495
PMCPMC7957971
OpenAlexW3109421243

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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.