Evidence map›Paper›PMID 36560800›Full record

ArticleViruses2022

Histone Deacetylase Inhibitor Panobinostat Benefits the Therapeutic Efficacy of Oncolytic Herpes Simplex Virus Combined with PD-1/PD-L1 Blocking in Glioma and Squamous Cell Carcinoma Models.

Yinglin Wu, Xiaoqing Chen, Lei Wang, Xusha Zhou, Yonghong Liu, Dongmei Ji, Peigen Ren, Grace Guoying Zhou, Jing Zhao

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Yinglin WuDepartment of Immunology, School of Basic Medical Sciences, Guangzhou Medical University, Guangzhou 511436, China.
Xiaoqing ChenShenzhen International Institute for Biomedical Research, Shenzhen 518110, China.
Lei WangShenzhen International Institute for Biomedical Research, Shenzhen 518110, China.
Xusha ZhouShenzhen International Institute for Biomedical Research, Shenzhen 518110, China.
Yonghong LiuShenzhen International Institute for Biomedical Research, Shenzhen 518110, China.
Dongmei JiDepartment of Medical Oncology, Shanghai Cancer Center and Shanghai Medical College, Fudan University, Shanghai 200032, China.
Peigen RenResearch Center for Reproduction and Health Development, Institute of Biomedicine and Biotechnology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.ORCID 0000-0002-6477-9055
Grace Guoying ZhouShenzhen International Institute for Biomedical Research, Shenzhen 518110, China.
Jing ZhaoShenzhen International Institute for Biomedical Research, Shenzhen 518110, China.
Shenzhen Institute of Information Technology · CNChinese Academy of Sciences · CNFudan University Shanghai Cancer Center · CNGuangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCombination therapy has been widely explored for oncolytic virus (OV), as it can be met with tumor resistance. The HDAC inhibitor (HDACi) panobinostat is a potent pan-deacetylase inhibitor which blocks multiple cancer-related pathways and reverses epigenetic events in cancer progression.

methodsIn this study, oncolytic activity in vitro and antitumor therapeutic efficacy in vivo when combined with oHSV and panobinostat were investigated.

results(1) Treatment with panobinostat enhanced oHSV propagation and cytotoxicity in human glioma A172 and squamous cell carcinoma SCC9 cells. (2) Combined treatment with oHSV and panobinostat enhanced virus replication mediated by the transcriptional downregulation of IFN-β- and IFN-responsive antiviral genes in human glioma A172 and squamous cell carcinoma SCC9 cells. (3) Panobinostat treatment induced upregulation of PD-L1 expression in both glioma and squamous cell carcinoma cells. (4) A significantly enhanced therapeutic efficacy was shown in vivo for the murine glioma CT-2A and squamous cell carcinoma SCC7 models when treated with a combination of oHSV, including PD-1/PD-L1 blockade and HDAC inhibition.

conclusionsConsequently, these data provide some new clues for the clinical development of combination therapy with OVs, epigenetic modifiers, and checkpoint blockades for glioma and squamous cell carcinoma.

Indexed as

Carcinoma, Squamous CellGliomaOncolytic VirotherapyOncolytic VirusesAnimalsB7-H1 AntigenCell Line, TumorHistone Deacetylase InhibitorsHumansMicePanobinostatProgrammed Cell Death 1 ReceptorSimplexvirusB7-H1 AntigenHistone Deacetylase InhibitorsPanobinostatProgrammed Cell Death 1 ReceptorgliomaHDACi panobinostatoHSVsquamous cell carcinoma

Identifiers

PMID36560800
PMCPMC9781547
OpenAlexW4311788264

What Socratic holds

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LicenceCC BY
Read underepoch 390

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 Socratic graph.