Evidence map›Paper›PMID 32372436›Full record

ArticleCancer science2020

EHF promotes colorectal carcinoma progression by activating TGF-β1 transcription and canonical TGF-β signaling.

Lan Wang, Meiling Ai, Miaoting Nie, Li Zhao, Guangxu Deng, Shasha Hu, Yue Han, Weiting Zeng, Yiqing Wang, Minhui Yang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  4. Exploring the Key Signaling Pathways and ncRNAs in Colorectal Cancer.International journal of molecular sciences · 2024
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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

11 authors at 2 institutions in 1 country.

Lan WangDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID https://orcid.org/0000-0003-3441-3199
Meiling AiDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Miaoting NieDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Li ZhaoDepartment of Pathology, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Guangxu DengDepartment of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Shasha HuDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yue HanDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Weiting ZengDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yiqing WangDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Minhui YangDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Shuang WangDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Nanfang Hospital · CNThird Affiliated Hospital of Guangzhou Medical University · CN

Funding

National Natural Science Foundation of China 81472318National Natural Science Foundation of China 81972754Natural Science Foundation of Guangdong Province 2019A1515012226
6 · The paper itself

Abstract

ETS homologous factor (EHF) plays a critical function in epithelial cell differentiation and proliferation. However, the roles of EHF in cancer remain largely unknown. In the present study, we investigated the expression levels, precise function and mechanism of EHF in colorectal carcinoma (CRC). We observed significantly elevated EHF expression in CRC cell lines and tissues. EHF overexpression correlated positively with poor differentiation, advanced T stage, and shorter overall survival of CRC patients. Function experiments revealed that EHF overexpression promoted CRC cell proliferation, migration, and invasion in vitro and in vivo. Mechanistically, EHF could directly upregulate transforming growth factor β1 (TGF-β1) expression at the transcription level, thereby activating canonical TGF-β signaling. Our findings provide novel insights into the mechanisms of EHF in tumorigenesis, invasion, and metastasis of CRC, which may help to provide new therapeutic targets for CRC intervention.

Indexed as

Signal TransductionTranscriptional ActivationAdultAgedAnimalsBiomarkers, TumorCell Line, TumorCell MovementCell ProliferationCell Transformation, NeoplasticColorectal NeoplasmsDisease Models, AnimalDisease ProgressionFemaleGene Expression Regulation, NeoplasticHeterograftsBiomarkers, TumorEHF protein, humanTranscription FactorsTransforming Growth Factor beta1colorectal carcinomaEHFproliferation and migrationTGF-β signalingtranscription factor

Identifiers

PMID32372436
PMCPMC7385339
OpenAlexW3023764605

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.