Evidence map›Paper›PMID 24427341›Full record

ArticleInternational journal of clinical and experimental pathology2014

Expression of HDAC9 in lung cancer--potential role in lung carcinogenesis.

Koji Okudela, Hideaki Mitsui, Takehisa Suzuki, Tetsukan Woo, Yoko Tateishi, Shigeaki Umeda, Yuichi Saito, Michihiko Tajiri, Munetaka Masuda, Kenichi Ohashi

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

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  10. MicroRNA-383-5p inhibits the progression of gastric carcinoma via targeting HDAC9 expression.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2019
    Article
  11. Review
  12. Overexpression ofOncoTargets and therapy · 2018
    Article
  13. Article
  14. Histone Modifications and Cancer.Cold Spring Harbor perspectives in biology · 2016
    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

10 authors at 2 institutions in 1 country.

Koji OkudelaDepartment of Pathology, Yokohama City University Graduate School of Medicine 3-9, Future, Kanazawaku, 236-0004, Yokohama, Japan.
Hideaki MitsuiDepartment of Pathology, Yokohama City University Graduate School of Medicine 3-9, Future, Kanazawaku, 236-0004, Yokohama, Japan.
Takehisa SuzukiDepartment of Pathology, Yokohama City University Graduate School of Medicine 3-9, Future, Kanazawaku, 236-0004, Yokohama, Japan.
Tetsukan WooDepartment of Surgery, Yokohama City University Graduate School of Medicine 3-9, Future, Kanazawaku, 236-0004, Yokohama, Japan.
Yoko TateishiDepartment of Pathology, Yokohama City University Graduate School of Medicine 3-9, Future, Kanazawaku, 236-0004, Yokohama, Japan.
Shigeaki UmedaDepartment of Pathology, Yokohama City University Graduate School of Medicine 3-9, Future, Kanazawaku, 236-0004, Yokohama, Japan.
Yuichi SaitoDepartment of Pathology, Yokohama City University Graduate School of Medicine 3-9, Future, Kanazawaku, 236-0004, Yokohama, Japan.
Michihiko TajiriDivision of General Thoracic Surgery, Kanagawa Prefectural Cardiovascular and Respiratory Center Hospital 6-16-1, Tomioka-higashi, Kanazawa-ku, 230-0051, Yokohama, Japan.
Munetaka MasudaDepartment of Surgery, Yokohama City University Graduate School of Medicine 3-9, Future, Kanazawaku, 236-0004, Yokohama, Japan.
Kenichi OhashiDepartment of Pathology, Yokohama City University Graduate School of Medicine 3-9, Future, Kanazawaku, 236-0004, Yokohama, Japan.
Yokohama City University · JPKanagawa Cardiovascular and Respiratory Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our previous studies identified important molecules involved in lung carcinogenesis through a comprehensive search for the downstream targets of oncogenic KRAS, and these findings suggested that an investigation into the downstream targets of oncogenic KRAS might represent a useful strategy for elucidating the common molecular bases of lung cancer. Among the downstream targets of oncogenic KRAS, a focus was placed on HDAC9, a member of the histone deacetylase family, in the present study because epigenetic modification of DNA or the histone proteins is known to play an important role in carcinogenesis. The immunohistochemical expression of HDAC9 was examined in surgically resected primary lung cancers (130 adenocarcinoma, 49 squamous cell carcinomas, one large cell carcinoma, and 6 small cell carcinomas) and potential associations between its expression level and pathologic factors were analyzed. The results showed that HDAC9 expression levels were lower in lung cancer cells than in non-tumor epithelial cells, and were also significantly lower in adenocarcinomas among the histological types. Moreover, HDAC9 expression levels were significantly lower in adenocarcinomas with lymphatic canal involvement. The restoration of HDAC9 in lung cancer cells losing its expression severely attenuated their growth activity in vitro. These results suggest that HDAC9 may be a suppressor and its downregulation might promote the progression process, especially in lung adenocarcinomas.

Indexed as

Blotting, WesternCarcinogenesisCarcinomaCell Line, TumorDisease ProgressionDown-RegulationHistone DeacetylasesHumansImmunohistochemistryLung NeoplasmsPolymerase Chain ReactionRepressor ProteinsTransfectionHDAC9 protein, humanHistone DeacetylasesRepressor ProteinsHDAC9KRASlung cancer

Identifiers

PMID24427341
PMCPMC3885475
OpenAlexW801564649

What OpenQuestion holds

Textmetadata
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.