Evidence map›Paper›PMID 28039460›Full record

ArticleOncotarget2017

Loss of FOXN3 in colon cancer activates beta-catenin/TCF signaling and promotes the growth and migration of cancer cells.

Yuedi Dai, Meixing Wang, Haixia Wu, Mi Xiao, Houbao Liu, Dexiang Zhang

RetractedOpen access · diamondAbstract readRetracted Publication
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.6field-weighted citation impact, top 10% 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, 40 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Yuedi DaiDepartment of Medical Oncology, Cancer Hospital of Fudan University, Minhang Branch, Shanghai 200240, China.
Meixing WangDepartment of Medical Oncology, Cancer Hospital of Fudan University, Minhang Branch, Shanghai 200240, China.
Haixia WuDepartment of Medical Oncology, Cancer Hospital of Fudan University, Minhang Branch, Shanghai 200240, China.
Mi XiaoDepartment of Medical Oncology, Cancer Hospital of Fudan University, Minhang Branch, Shanghai 200240, China.
Houbao LiuGeneral Surgery Department, General Surgery Institute, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Dexiang ZhangGeneral Surgery Department, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai 200240, China.
Fudan University Shanghai Cancer Center · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant activation of beta-catenin/TCF is a hallmark of colon cancer. How the functions of nuclear localized beta-catenin are regulated is not fully understood. Here, it was found that FOXN3 (Forkhead box N3) was down-regulated in colon cancer tissues. Forced expression of FOXN3 inhibited the growth, migration and invasion of colon cancer cells, while knocking down the expression of FOXN3 promoted the growth, migration, invasion and metastasis of colon cancer cells. FOXN3 bind to beta-catenin and inhibited beta-catenin/TCF signaling by blocking the interaction between beta-catenin and TCF4. Taken together, these data demonstrated the suppressive roles of FOXN3 in the progression of colon cancer, and indicated that restoring the functions of FOXN3 would be a novel therapeutic strategy for colon cancer.

Indexed as

Cell MovementCell ProliferationAnimalsbeta CateninCell Cycle ProteinsCell Line, TumorColonic NeoplasmsForkhead Transcription FactorsGene Expression Regulation, NeoplasticHumansMice, NudeMice, TransgenicNeoplasm InvasivenessNeoplasm MetastasisProtein BindingRepressor Proteinsbeta CateninCell Cycle ProteinsCTNNB1 protein, humanForkhead Transcription FactorsFOXN3 protein, humanRepressor ProteinsTCF4 protein, humanTranscription Factor 4beta-catenin/TCF signalingcell growth and migrationcolon cancerFOXN3

Identifiers

PMID28039460
PMCPMC5354770
OpenAlexW2563740832

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.