Evidence map›Paper›PMID 32732864›Full record

ArticleCell death & disease2020

EN2 as an oncogene promotes tumor progression via regulating CCL20 in colorectal cancer.

Yimin Li, Jiaxin Liu, Qing Xiao, Ruotong Tian, Zhengwei Zhou, Yaqi Gan, Yuanyuan Li, Guang Shu, Gang Yin

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
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

27 citing papers in PubMed, 40 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

9 authors at 1 institution in 1 country.

Yimin Li *Department of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Jiaxin Liu *Department of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Qing XiaoDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Ruotong TianSchool of Basic Medical Sciences, Central South University, Changsha, Hunan Province, China.
Zhengwei ZhouSchool of Basic Medical Sciences, Central South University, Changsha, Hunan Province, China.
Yaqi GanDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Yuanyuan LiDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Guang ShuSchool of Basic Medical Sciences, Central South University, Changsha, Hunan Province, China. shuguang78@csu.edu.cn.
Gang YinDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China. gangyin@csu.edu.cn.ORCID http://orcid.org/0000-0003-3753-0753
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Engrailed-2 (EN2), a member of the engrailed homeobox family, has been shown to be abnormally expressed in a variety of cancers. However, the expression and the clinical significance of EN2 in colorectal cancer (CRC) are largely unknown. Firstly, we found that EN2 acted as an oncogene in CRC. EN2 was upregulated in colorectal cancer tissues compared with adjacent normal tissues. Higher EN2 expression was significantly associated with poorer survival rate. Knockdown of EN2 markedly inhibited proliferation and migration capacities of SW480 cells in vitro, and suppressed tumorigenicity in vivo. Mechanistically, Chemokine ligand 20 (CCL20), a member of the C-C motif chemokine subfamily, was identified as a direct target gene of EN2 in CRC. CCL20 expression was positively correlated with EN2 expression in CRC tissues. Moreover, EN2 promoted the proliferation and migration of CRC cells by regulating the expression of CCL20 in vitro. These results suggest that EN2 plays a critical role in the CRC tumor progression and may serve as a potential target for CRC prevention and therapy.

Indexed as

Disease ProgressionGene Expression Regulation, NeoplasticOncogenesAgedAnimalsBase SequenceCarcinogenesisCell Line, TumorCell MovementCell NucleusCell ProliferationChemokine CCL20Colorectal NeoplasmsEngrailed 2 ProteinFemaleGene Knockdown TechniquesCCL20 protein, humanChemokine CCL20Engrailed 2 ProteinHomeodomain ProteinsNerve Tissue Proteins

Identifiers

PMID32732864
PMCPMC7393501
OpenAlexW3046204841

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.