Evidence map›Paper›PMID 30131570›Full record

ArticleScientific reports2018

HDAC4 degradation by combined TRAIL and valproic acid treatment induces apoptotic cell death of TRAIL-resistant head and neck cancer cells.

Bok-Soon Lee, Yeon Soo Kim, Haeng-Jun Kim, Dae-Ho Kim, Ho-Ryun Won, Yong-Sung Kim, Chul-Ho Kim

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

12 citing papers in PubMed, 16 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

7 authors at 3 institutions in 1 country.

Bok-Soon LeeDepartment of Otolaryngology, School of Medicine, Ajou University, Suwon, 16499, Republic of Korea.
Yeon Soo KimDepartment of Otorhinolaryngology, College of Medicine, Konyang University Hospital, Konyang University Myunggok Medical Research Institute, Daejeon, 35365, Republic of Korea.
Haeng-Jun KimDepartment of Otolaryngology, School of Medicine, Ajou University, Suwon, 16499, Republic of Korea.
Dae-Ho KimDepartment of Otolaryngology, School of Medicine, Ajou University, Suwon, 16499, Republic of Korea.
Ho-Ryun WonDepartment of Otolaryngology, School of Medicine, Ajou University, Suwon, 16499, Republic of Korea.
Yong-Sung KimDepartment of Molecular Science and Technology, Ajou University, Suwon, 16499, Republic of Korea.ORCID 0000-0003-2673-1509
Chul-Ho KimDepartment of Otolaryngology, School of Medicine, Ajou University, Suwon, 16499, Republic of Korea. ostium@ajou.ac.kr.
Ajou University · KRKonyang University · KRChungnam National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although TRAIL can directly induce cell death in some cancer cells, it appears that TRAIL resistance exists in many cancers. This study focuses on anti-cancer drugs for TRAIL-resistant head and neck cancer (HNC) to provide further progress toward effective cancer therapy. Results indicate in TRAIL-resistant HNC cells, that combined TRAIL and VPA treatment greatly reduced cell viability and therefore induced cell death, relative to treatment with TRAIL or VPA alone. A caspase-dependent signaling pathway was demonstrated, and combined treatment with TRAIL and VPA also significantly decreased the expression of HDAC4. When we pretreated cells with z-VAD followed by combined treatment with TRAIL and VPA, cell death was blocked with no reduction in expression of HDAC4. To confirm that cell death involved HDAC4 in HNC cells, we knocked down expression of HDAC4 with siRNA, followed by treatment with TRAIL and VPA. Results showed that loss of HDAC4 sensitized the TRAIL-resistant HNC cells to apoptotic cell death. Finally, we showed elevated expression of HDAC4 in HNC tissues compared to normal tissues obtained from the same patients. In conclusion, we suggest that combined VPA and TRAIL treatment may be a promising therapy for HNC via HDAC4 degradation.

Indexed as

CaspasesCell Line, TumorCell ProliferationCell SurvivalDrug Resistance, NeoplasmDrug SynergismGene Expression Regulation, NeoplasticGene Knockdown TechniquesHead and Neck NeoplasmsHistone DeacetylasesHumansProteolysisRepressor ProteinsSignal TransductionTNF-Related Apoptosis-Inducing LigandUp-RegulationCaspasesHDAC4 protein, humanHistone DeacetylasesRepressor ProteinsTNF-Related Apoptosis-Inducing LigandValproic Acid

Identifiers

PMID30131570
PMCPMC6104079
OpenAlexW2886602248

What OpenQuestion 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 OpenQuestion graph.