Evidence map›Paper›PMID 29311643›Full record

ArticleOncogene2018

LncRNA-NEF antagonized epithelial to mesenchymal transition and cancer metastasis via cis-regulating FOXA2 and inactivating Wnt/β-catenin signaling.

Wei-Cheng Liang, Jia-Lin Ren, Cheuk-Wa Wong, Sun-On Chan, Mary Miu-Yee Waye, Wei-Ming Fu, Jin-Fang Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
6.4field-weighted citation impact, top 2% 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

73 citing papers in PubMed, 126 citations in OpenAlex.

  1. Trial
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  3. Review
  4. HPV-Independent Cervical Cancer-A New Challenge of Modern Oncology.International journal of molecular sciences · 2025
    Review
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  7. Integration analysis ofBiochemistry and biophysics reports · 2024
    Article
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  11. Article
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  20. Article

13 more citing papers are in PubMed but not listed here.

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

7 authors at 3 institutions in 1 country.

Wei-Cheng LiangSchool of Biomedical Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, PR China.
Jia-Lin RenSchool of Biomedical Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, PR China.
Cheuk-Wa WongSchool of Biomedical Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, PR China.
Sun-On ChanSchool of Biomedical Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, PR China.
Mary Miu-Yee WayeSchool of Biomedical Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, PR China.
Wei-Ming FuSchool of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, PR China. fuweiming76@smu.edu.cn.
Jin-Fang ZhangKey Laboratory of Orthopaedics and Traumatology, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, The First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, PR China. zhangjf06@cuhk.edu.hk.
Chinese University of Hong Kong · CNFirst Affiliated Hospital of Guangzhou University of Chinese Medicine · CNSouthern Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging evidence indicates that the long noncoding RNAs extensively participate in cancer progression. Nevertheless, the molecular pathogenesis of how these lncRNAs regulate tumorigenesis has not been fully elucidated especially in hepatocellular carcinoma (HCC). Here, we sought to define the role of a novel lncRNA named lncRNA-NEF in modulating epithelial to mesenchymal transition (EMT) in HCC. It was found that the lncRNA-NEF was transcriptionally activated by EMT suppressor FOXA2 and frequently downregulated in HCC cell lines as well as clinical specimens. Although enhanced expression of lncRNA-NEF did not affect tumor cell growth, ectopic expression of lncRNA-NEF significantly suppressed EMT program and cell migration. Animal studies validated that lncRNA-NEF alleviated in vivo tumor metastasis and protected mice from tumor-induced mortality. Interestingly, we verified that lncRNA-NEF acted as a novel activator of its neighbor gene FOXA2, which formed a positive feedback loop. Subsequent studies revealed that lncRNA-NEF physically interacted with β-catenin to increase the binding of GSK3β with β-catenin and therefore promoted the inhibitory phosphorylation of β-catenin, leading to the suppression on Wnt/β-catenin signaling and activation of FOXA2 expression. Hence, our findings illustrated a novel feedback loop including FOXA2 and its neighboring gene lncRNA-NEF, which might provide mechanistic insights into the metastatic progress of HCC.

Indexed as

Animalsbeta CateninCell Line, TumorDown-RegulationEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHEK293 CellsHepatocyte Nuclear Factor 3-betaHumansMiceMice, Inbred BALB CMice, NudeNeoplasm MetastasisRNA, Long NoncodingWnt Signaling Pathwaybeta CateninFOXA2 protein, humanHepatocyte Nuclear Factor 3-betaRNA, Long Noncoding

Identifiers

PMID29311643
OpenAlexW2781945015

What OpenQuestion holds

Textmetadata
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.