Evidence map›Paper›PMID 26824987›Full record

ArticleOncotarget2016

Dehydropeptidase 1 promotes metastasis through regulation of E-cadherin expression in colon cancer.

Sang Yoon Park, Seon-Jin Lee, Hee Jun Cho, Tae Woo Kim, Jong-Tae Kim, Jae Wha Kim, Chul-Ho Lee, Bo-Yeon Kim, Young Il Yeom, Jong-Seok Lim and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 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

12 authors at 4 institutions in 1 country.

Sang Yoon ParkGenome Structure Research Center, Korea Research Institute of Biosceience and Biotechnology, Daejeon, Korea.
Seon-Jin LeeGenome Structure Research Center, Korea Research Institute of Biosceience and Biotechnology, Daejeon, Korea.
Hee Jun ChoGenome Structure Research Center, Korea Research Institute of Biosceience and Biotechnology, Daejeon, Korea.
Tae Woo KimGenome Structure Research Center, Korea Research Institute of Biosceience and Biotechnology, Daejeon, Korea.
Jong-Tae KimGenome Structure Research Center, Korea Research Institute of Biosceience and Biotechnology, Daejeon, Korea.
Jae Wha KimBiomedical Translational Research Center, Korea Research Institute of Biosceience and Biotechnology, Daejeon, Korea.
Chul-Ho LeeAnimal Resource Center, Korea Research Institute of Biosceience and Biotechnology, Daejeon, Korea.
Bo-Yeon KimWorld Class Institute, Korea Research Institute of Bioscience and Biotechnology, Cheongju, Korea.
Young Il YeomDepartment of Functional Genomics, Korea Research Institute of Biosceience and Biotechnology, Daejeon, Korea.
Jong-Seok LimDepartment of Biological Sciences, and The Research Center for Women's Diseases, Sookmyung Women's University, Seoul, Korea.
Younghee LeeDepartment of Biochemistry, College of Natural Sciences, Chungbuk National University, Cheongju, Korea.
Hee Gu LeeGenome Structure Research Center, Korea Research Institute of Biosceience and Biotechnology, Daejeon, Korea.
Korea Research Institute of Bioscience and Biotechnology · KRKorea University of Science and Technology · KRChungbuk National University · KRSookmyung Women's University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dehydropeptidase 1 (DPEP1) is a zinc-dependent metalloproteinase that is expressed aberrantly in several cancers. The role of DPEP1 in cancer remain controversial. In this study, we demonstrate that DPEP1 functions as a positive regulator for colon cancer cell metastasis. The expression of DPEP1 mRNA and proteins were upregulated in colon cancer tissues compared to normal mucosa. Gain-of-function and loss-of-function approaches were used to examine the malignant phenotype of DPEP1-expressing or DPEP1-depleted cells. DPEP1 expression caused a significant increase in colon cancer cell adhesion and invasion in vitro, and metastasis in vivo. In contrast, DPEP1 depletion induced opposite effects. Furthermore, cilastatin, a DPEP1 inhibitor, suppressed the invasion and metastasis of DPEP1-expressing cells. DPEP1 inhibited the leukotriene D4 signaling pathway and increased the expression of E-cadherin. We also show that DPEP1 mediates TGF-β-induced EMT. TGF-β transcriptionally repressed DPEP1 expression. TGF-β treatment decreased E-cadherin expression and promoted cell invasion in DPEP1-expressing colon cancer cell lines, whereas it did not affect these parameters in DPEP1-depleted cell lines. These results suggest that DPEP1 promotes cancer metastasis by regulating E-cadherin plasticity and that it might be a potential therapeutic target for preventing the progression of colon cancer.

Indexed as

AnimalsAntigens, CDCadherinsCell AdhesionCell Line, TumorCilastatinColonic NeoplasmsDipeptidasesEpithelial-Mesenchymal TransitionFemaleGPI-Linked ProteinsHCT116 CellsHT29 CellsHumansLeukotriene D4Liver NeoplasmsAntigens, CDCadherinsCDH1 protein, humanCilastatindipeptidase 1DipeptidasesGPI-Linked ProteinsLeukotriene D4RNA, MessengerRNA, Small InterferingTransforming Growth Factor betacolon cancerdehydropeptidase 1E-cadherininvasionmetastasis

Identifiers

PMID26824987
PMCPMC4891055
OpenAlexW2303834781

What OpenQuestion holds

Textmetadata
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.