Evidence map›Paper›PMID 29669932›Full record

ArticleJCI insight2018

Nardilysin controls intestinal tumorigenesis through HDAC1/p53-dependent transcriptional regulation.

Keitaro Kanda, Jiro Sakamoto, Yoshihide Matsumoto, Kozo Ikuta, Norihiro Goto, Yusuke Morita, Mikiko Ohno, Kiyoto Nishi, Koji Eto, Yuto Kimura and 12 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. The histone deacetylase family in health and disease.Signal transduction and targeted therapy · 2026
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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

22 authors at 4 institutions in 2 countries.

Keitaro KandaDepartment of Gastroenterology and Hepatology, and.
Jiro SakamotoDepartment of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Yoshihide MatsumotoDepartment of Gastroenterology and Hepatology, and.
Kozo IkutaDepartment of Gastroenterology and Hepatology, and.
Norihiro GotoDepartment of Gastroenterology and Hepatology, and.
Yusuke MoritaDepartment of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Mikiko OhnoDepartment of Pharmacology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Kiyoto NishiDepartment of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Koji EtoDepartment of Clinical Application, Center for iPS Cell Research and Application, Kyoto, Japan.
Yuto KimuraDepartment of Gastroenterology and Hepatology, and.
Yuki NakanishiDepartment of Gastroenterology and Hepatology, and.
Kanako IkegamiDepartment of Gastroenterology and Hepatology, and.
Takaaki YoshikawaDepartment of Gastroenterology and Hepatology, and.
Akihisa FukudaDepartment of Gastroenterology and Hepatology, and.
Kenji KawadaDepartment of Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Yoshiharu SakaiDepartment of Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Akihiro ItoChemical Genetics Laboratory, RIKEN, Wako, Saitama, Japan.
Minoru YoshidaChemical Genetics Laboratory, RIKEN, Wako, Saitama, Japan.
Takeshi KimuraDepartment of Cardiovascular Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Tsutomu ChibaDepartment of Gastroenterology and Hepatology, and.
Eiichiro NishiDepartment of Pharmacology, Shiga University of Medical Science, Otsu, Shiga, Japan.
Hiroshi SenoDepartment of Gastroenterology and Hepatology, and.
Kyoto University · JPRIKEN Center for Sustainable Resource Science · JPShiga University of Medical Science · JPRemote Sensing Application Center · BG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colon cancer is a complex disease affected by a combination of genetic and epigenetic factors. Here we demonstrate that nardilysin (N-arginine dibasic convertase; NRDC), a metalloendopeptidase of the M16 family, regulates intestinal tumorigenesis via its nuclear functions. NRDC is highly expressed in human colorectal cancers. Deletion of the Nrdc gene in ApcMin mice crucially suppressed intestinal tumor development. In ApcMin mice, epithelial cell-specific deletion of Nrdc recapitulated the tumor suppression observed in Nrdc-null mice. Moreover, epithelial cell-specific overexpression of Nrdc significantly enhanced tumor formation in ApcMin mice. Notably, epithelial NRDC controlled cell apoptosis in a gene dosage-dependent manner. In human colon cancer cells, nuclear NRDC directly associated with HDAC1, and controlled both acetylation and stabilization of p53, with alterations of p53 target apoptotic factors. These findings demonstrate that NRDC is critically involved in intestinal tumorigenesis through its epigenetic regulatory function, and targeting NRDC may lead to a novel prevention or therapeutic strategy against colon cancer.

Indexed as

AdultAgedAnimalsCarcinogenesisColorectal NeoplasmsDisease Models, AnimalEpigenomicsFemaleGene DeletionHistone Deacetylase 1HumansMaleMetalloendopeptidasesMiceMiddle AgedNeoplasm StagingHDAC1 protein, humanHistone Deacetylase 1MetalloendopeptidasesnardilysinNRDC protein, humanTumor Suppressor Protein p53Colorectal cancerOncology

Identifiers

PMID29669932
PMCPMC5931127
OpenAlexW2799277498

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.