Evidence map›Paper›PMID 26473836›Full record

ArticleInternational journal of molecular sciences2015

Increased Histone Deacetylase Activity Involved in the Suppressed Invasion of Cancer Cells Survived from ALA-Mediated Photodynamic Treatment.

Pei-Tzu Li, Yi-Jane Tsai, Ming-Jen Lee, Chin-Tin Chen

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

9 citing papers in PubMed, 19 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

4 authors at 2 institutions in 1 country.

Pei-Tzu LiDepartment of Biochemical Science and Technology, National Taiwan University, Taipei 106, Taiwan. peitzuli@gmail.com.
Yi-Jane TsaiDepartment of Biochemical Science and Technology, National Taiwan University, Taipei 106, Taiwan. jane19841114@hotmail.com.
Ming-Jen LeeDepartment of Neurology, National Taiwan University Hospital, 7, Chung-Shan South Road, Taipei 100, Taiwan. mjlee@ntu.edu.tw.
Chin-Tin ChenDepartment of Biochemical Science and Technology, National Taiwan University, Taipei 106, Taiwan. chintin@ntu.edu.tw.
National Taiwan University · TWNational Taiwan University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previously, we have found that cancer cells survived from 5-Aminolevulinic acid-mediated photodynamic therapy (ALA-PDT) have abnormal mitochondrial function and suppressed cellular invasiveness. Here we report that both the mRNA expression level and enzymatic activity of histone deacetylase (HDAC) were elevated in the PDT-derived variants with dysfunctional mitochondria. The activated HDAC deacetylated histone H3 and further resulted in the reduced migration and invasion, which correlated with the reduced expression of the invasion-related genes, matrix metalloproteinase 9 (MMP9), paternally expressed gene 1 (PEG1), and miR-355, the intronic miRNA. Using chromatin immunoprecipitation, we further demonstrate the reduced amount of acetylated histone H3 on the promoter regions of MMP9 and PEG1, supporting the down-regulation of these two genes in PDT-derived variants. These results indicate that HDAC activation induced by mitochondrial dysfunction could modulate the cellular invasiveness and its related gene expression. This argument was further verified in the 51-10 cybrid cells with the 4977 bp mtDNA deletion and A375 ρ⁰ cells with depleted mitochondria. These results indicate that mitochondrial dysfunction might suppress tumor invasion through modulating histone acetylation.

Indexed as

AcetylationAminolevulinic AcidAzacitidineCell Line, TumorCell MovementChromatin ImmunoprecipitationHistone Deacetylase InhibitorsHistone DeacetylasesHistonesHumansHydroxamic AcidsMatrix Metalloproteinase 9MicroRNAsMitochondriaNeoplasm InvasivenessPhotochemotherapyAminolevulinic AcidAzacitidineHistone Deacetylase InhibitorsHistone DeacetylasesHistonesHydroxamic AcidsMatrix Metalloproteinase 9mesoderm specific transcript proteinMicroRNAsMIRN355 microRNA, humanMMP9 protein, humanProteinstrichostatin Ahistone acetylationhistone deacetylaseinvasionmetalloproteinase 9mitochondriapaternally expressed gene 1

Identifiers

PMID26473836
PMCPMC4632734
OpenAlexW1935109088

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.