Evidence map›Paper›PMID 23610444›Full record

ArticleCancer research2013

DDB2 suppresses epithelial-to-mesenchymal transition in colon cancer.

Nilotpal Roy, Prashant V Bommi, Uppoor G Bhat, Shaumick Bhattacharjee, Indira Elangovan, Jing Li, Krushna C Patra, Dragana Kopanja, Adam Blunier, Richard Benya and 2 more

Abstract read
In one paragraph

Article in Cancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

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  16. LOC101060264 Silencing Suppresses Invasion and Metastasis of Human Colon Cancer.Medical science monitor : international medical journal of experimental and clinical research · 2020
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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 1 institution in 1 country.

Nilotpal RoyDepartment of Biochemistry and Molecular Genetics; Center of Molecular Biology of Oral Diseases College of Dentistry, Cancer Center; and Department of Medicine, University of Illinois at Chicago, Chicago, IL 60612, USA.
Prashant V Bommi
Uppoor G Bhat
Shaumick Bhattacharjee
Indira Elangovan
Jing Li
Krushna C Patra
Dragana Kopanja
Adam Blunier
Richard Benya
Srilata Bagchi
Pradip Raychaudhuri
University of Illinois Chicago · US

Funding

Role of DDB in Checkpoint Control and CarcinogenesisR01CA077637 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI RAYCHAUDHURI, PRADIP · 1999 to 2014
$3.6M
DNA Damage Response and DDBR01CA156164 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI BAGCHI, SRILATA, RAYCHAUDHURI, PRADIP · 2010 to 2014
$1.6M
NCI NIH HHS CA 156164NCI NIH HHS CA77637NCI NIH HHS R01 CA077637NCI NIH HHS R01 CA156164
6 · The paper itself

Abstract

Colon cancer is one of the deadliest cancers worldwide because of its metastasis to other essential organs. Metastasis of colon cancer involves a complex set of events, including epithelial-to-mesenchymal transition (EMT) that increases invasiveness of the tumor cells. Here, we show that the xeroderma pigmentosum group E (XPE) gene product, damaged DNA-binding protein (DDB)-2, is downregulated in high-grade colon cancers, and it plays a dominant role in the suppression of EMT of the colon cancer cells. Depletion of DDB2 promotes mesenchymal phenotype, whereas expression of DDB2 promotes epithelial phenotype. DDB2 constitutively represses genes that are the key activators of EMT, indicating that DDB2 is a master regulator of EMT of the colon cancer cells. Moreover, we observed evidence that DDB2 functions as a barrier for EMT induced by hypoxia and TGF-β. Also, we provide evidence that DDB2 inhibits metastasis of colon cancer. The results presented here identify a transcriptional regulatory pathway of DDB2 that is directly linked to the mechanisms that suppress metastasis of colon cancer.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBlotting, WesternCadherinsCell HypoxiaCell Line, TumorColonic NeoplasmsDNA-Binding ProteinsEpithelial-Mesenchymal TransitionHCT116 CellsHumansImmunohistochemistryLung NeoplasmsMaleMammary Neoplasms, ExperimentalMiceCadherinsDDB2 protein, humanDNA-Binding Proteins

Identifiers

PMID23610444
PMCPMC3686976
OpenAlexW2126109638

What OpenQuestion holds

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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.