Evidence map›Paper›PMID 30065760›Full record

ArticleCellular & molecular biology letters2018

Droxinostat sensitizes human colon cancer cells to apoptotic cell death via induction of oxidative stress.

Ying Huang, Wuping Yang, Huihong Zeng, Chuan Hu, Yaqiong Zhang, Nanhua Ding, Guangqin Fan, Lijian Shao, Bohai Kuang

Abstract read
In one paragraph

Article in Cellular & molecular biology letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
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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.

Ying Huang *1Jiangxi provincial key laboratory of preventive medicine, Nanchang University, Nanchang, 330006 China.
Wuping Yang *1Jiangxi provincial key laboratory of preventive medicine, Nanchang University, Nanchang, 330006 China.
Huihong Zeng *2Medical School of Nanchang University, 461 Bayi Road, Nanchang, 330006 Jiangxi China.
Chuan Hu2Medical School of Nanchang University, 461 Bayi Road, Nanchang, 330006 Jiangxi China.
Yaqiong Zhang2Medical School of Nanchang University, 461 Bayi Road, Nanchang, 330006 Jiangxi China.
Nanhua Ding2Medical School of Nanchang University, 461 Bayi Road, Nanchang, 330006 Jiangxi China.
Guangqin Fan1Jiangxi provincial key laboratory of preventive medicine, Nanchang University, Nanchang, 330006 China.
Lijian Shao1Jiangxi provincial key laboratory of preventive medicine, Nanchang University, Nanchang, 330006 China.
Bohai Kuang2Medical School of Nanchang University, 461 Bayi Road, Nanchang, 330006 Jiangxi China.ORCID 0000-0002-7814-8406

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Upregulation of histone acetylation plays a critical role in the dysregulation of transcription. It alters the structure of chromatin, which leads to the onset of cancer. Histone deacetylase inhibitors may therefore be a promising way to limit cancer progression. In this study, we examined the effects of droxinostat on the growth of HT-29 colon cancer cells. Our results show that droxinostat effectively inhibited cell growth and colony-forming ability by inducing cellular apoptosis and ROS production in HT-29 cells. Notably, the apoptotic inhibitor Z-VAD-FMK significantly decreased the levels of cellular apoptosis and the antioxidant γ-tocotrienol (GT3) significantly decreased ROS production induced by droxinostat treatment. Z-VAD-FMK and GT3 also partially reversed the negative growth effects of droxinstat on HT-29 cells. GT3 treatment decreased cellular apoptosis and increased colony-forming ability upon droxinostat administration. Z-VAD-FMK treatment also partially decreased droxinostat-induced ROS production. Our findings suggest that the effects of droxinostat on colon cancer cells are mediated by the induction of oxidative stress and apoptotic cell death.

Indexed as

Amino Acid Chloromethyl KetonesApoptosisColonic NeoplasmsHistone Deacetylase InhibitorsHT29 CellsHumansHydroxamic AcidsOxidative StressReactive Oxygen Species4-(4-chloro-2-methylphenoxy)-N-hydroxybutanamideAmino Acid Chloromethyl Ketonesbenzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketoneHistone Deacetylase InhibitorsHydroxamic AcidsReactive Oxygen SpeciesApoptosisDroxinostatHT-29 cellsROS

Identifiers

PMID30065760
PMCPMC6064062

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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.