Evidence map›Paper›PMID 25340858›Full record

ArticlePloS one2014

Mechanisms underlying cancer growth and apoptosis by DEK overexpression in colorectal cancer.

Lijuan Lin, Junjie Piao, Yibing Ma, Tiefeng Jin, Chengshi Quan, Jienan Kong, Yulin Li, Zhenhua Lin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 28 citations in OpenAlex.

  1. 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

8 authors at 4 institutions in 1 country.

Lijuan LinDepartment of Pathology & Cancer Research Center, Yanbian University Medical College, Yanji, China; Department of Medical Imaging, College of Medicine, Eastern Liaoning University, Dandong, China.
Junjie PiaoDepartment of Pathology & Cancer Research Center, Yanbian University Medical College, Yanji, China.
Yibing MaDepartment of Pathology, Dandong Centre Hospital, Dandong, China.
Tiefeng JinDepartment of Pathology & Cancer Research Center, Yanbian University Medical College, Yanji, China.
Chengshi QuanThe Key Laboratory of Pathobiology, Ministry of Education, Bethune Medical College, Jilin University, Changchun, China.
Jienan KongDepartment of Pathology & Cancer Research Center, Yanbian University Medical College, Yanji, China.
Yulin LiThe Key Laboratory of Pathobiology, Ministry of Education, Bethune Medical College, Jilin University, Changchun, China.
Zhenhua LinDepartment of Pathology & Cancer Research Center, Yanbian University Medical College, Yanji, China.
Yanbian University · CNJilin University · CNEastern Liaoning University · CNWuhan Wudong Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our previous study indicated that DEK protein was overexpressed in colorectal carcinoma (CRC) compared with the normal colorectal mucosa. DEK was also significantly correlated with the prognostic characteristics of patients with CRC, demonstrating that DEK played an important role in CRC progression. In this work, we evaluate the effects of DEK on biological behaviors in CRC and explore the related molecular mechanisms. The results showed that DEK was overexpressed in human CRC tissues, and was correlated with the Ki-67 index and the apoptotic index. DEK depletion by RNAi in SW-620 and HCT116 cells significantly decreased cell proliferation, but increased cell apoptosis. Upregulation of DEK was involved in the p53/MDM, Bcl-2 family, and caspase pathways. Our study demonstrates that DEK promotes the growth of CRC, and could be a therapeutic target in CRC.

Indexed as

ApoptosisCell Line, TumorCell ProliferationChromosomal Proteins, Non-HistoneColorectal NeoplasmsDisease ProgressionGene Expression ProfilingHCT116 CellsHumansImmunohistochemistryIntestinal MucosaKi-67 AntigenMicroscopy, FluorescenceOncogene ProteinsPoly-ADP-Ribose Binding ProteinsProto-Oncogene Proteins c-bcl-2BCL2 protein, humanChromosomal Proteins, Non-HistoneDEK protein, humanKi-67 AntigenOncogene ProteinsPoly-ADP-Ribose Binding ProteinsProto-Oncogene Proteins c-bcl-2RNA, Small InterferingTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID25340858
PMCPMC4207817
OpenAlexW2019069224

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.