Evidence map›Paper›PMID 25973305›Full record

ArticleAmerican journal of cancer research2015

Histone deacetylase 3 inhibits new tumor suppressor gene DTWD1 in gastric cancer.

Yanning Ma, Yongfang Yue, Min Pan, Jie Sun, Jue Chu, Xiaoying Lin, Wenxia Xu, Lifeng Feng, Yan Chen, Dingwei Chen and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

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  19. Epigenetic roles in the malignant transformation of gastric mucosal cells.Cellular and molecular life sciences : CMLS · 2016
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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

13 authors at 3 institutions in 2 countries.

Yanning MaLaboratory of Cancer Biology, Department of Medical Oncology, Key laboratory of Biotherapy in Zhejiang Province, Sir Runrun Shaw Hospital Zhejiang University, China.
Yongfang YueLaboratory of Cancer Biology, Department of Medical Oncology, Key laboratory of Biotherapy in Zhejiang Province, Sir Runrun Shaw Hospital Zhejiang University, China.
Min PanLaboratory of Cancer Biology, Department of Medical Oncology, Key laboratory of Biotherapy in Zhejiang Province, Sir Runrun Shaw Hospital Zhejiang University, China.
Jie SunLaboratory of Cancer Biology, Department of Medical Oncology, Key laboratory of Biotherapy in Zhejiang Province, Sir Runrun Shaw Hospital Zhejiang University, China.
Jue ChuLaboratory of Cancer Biology, Department of Medical Oncology, Key laboratory of Biotherapy in Zhejiang Province, Sir Runrun Shaw Hospital Zhejiang University, China.
Xiaoying LinLaboratory of Cancer Biology, Department of Medical Oncology, Key laboratory of Biotherapy in Zhejiang Province, Sir Runrun Shaw Hospital Zhejiang University, China.
Wenxia XuLaboratory of Cancer Biology, Department of Medical Oncology, Key laboratory of Biotherapy in Zhejiang Province, Sir Runrun Shaw Hospital Zhejiang University, China.
Lifeng FengLaboratory of Cancer Biology, Department of Medical Oncology, Key laboratory of Biotherapy in Zhejiang Province, Sir Runrun Shaw Hospital Zhejiang University, China.
Yan ChenDepartrment of Gastroenterology, The 2nd Hospital of Zhejiang University China.
Dingwei ChenLaboratory of Cancer Biology, Department of Medical Oncology, Key laboratory of Biotherapy in Zhejiang Province, Sir Runrun Shaw Hospital Zhejiang University, China.
Vivian Y ShinDepartrment of Surgery, The University of Hong Kong China.
Xian WangLaboratory of Cancer Biology, Department of Medical Oncology, Key laboratory of Biotherapy in Zhejiang Province, Sir Runrun Shaw Hospital Zhejiang University, China.
Hongchuan JinLaboratory of Cancer Biology, Department of Medical Oncology, Key laboratory of Biotherapy in Zhejiang Province, Sir Runrun Shaw Hospital Zhejiang University, China.
Sir Run Run Shaw Hospital · CNUniversity of Hong Kong · HKZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer epigenetics plays an important role in the pathogenesis of many cancers including gastric cancer. Histone deacetylases (HDACs) emerge as exciting therapeutic targets for cancer treatment and prevention. In this study, we identified DTWD1 as one of the 122 genes upregulated after treatment of trichostatin A (TSA) in two gastric cancer cell lines. Moreover, DTWD1 was downregulated in gastric cancer cell lines and primary gastric carcinoma tissues. It was further identified as the new target of p53. Then we revealed that HDAC3 downregulated DTWD1 by disrupting the interaction of p53 with DTWD1 promoter. Furthermore, DTWD1 functioned as a tumor suppressor by downregulating cyclin B1 expression to inhibit proliferation. In summary, as the new p53 target gene, DTWD1 was downregulated in gastric cancer by HDAC3 and acted as a novel tumor suppressor gene. Specific inhibitors of HDAC3 might be a new approach for gastric cancer treatment by activating DTWD1 expression.

Indexed as

DTWD1gastric cancerHDACp53tumor suppressor gene

Identifiers

PMID25973305
PMCPMC4396045
OpenAlexW218921945

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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.