Evidence map›Paper›PMID 30950191›Full record

ArticleJournal of cellular and molecular medicine2019

Overexpression of ZEB2-AS1 promotes epithelial-to-mesenchymal transition and metastasis by stabilizing ZEB2 mRNA in head neck squamous cell carcinoma.

Pengfei Diao, Han Ge, Yue Song, Yaping Wu, Jin Li, Zhongwu Li, Jianrong Yang, Yanling Wang, Jie Cheng

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
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  9. The Hypoxia-Long Noncoding RNA Interaction in Solid Cancers.International journal of molecular sciences · 2021
    Review
  10. The Long Non-Coding RNAOncoTargets and therapy · 2020
    Article
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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.

Pengfei DiaoJiangsu Key Laboratory of Oral Disease, Nanjing Medical University, Nanjing, China.
Han GeDepartment of Oral and Maxillofacial Surgery, Affiliated Stomatological Hospital, Nanjing Medical University, Nanjing, China.
Yue SongJiangsu Key Laboratory of Oral Disease, Nanjing Medical University, Nanjing, China.
Yaping WuJiangsu Key Laboratory of Oral Disease, Nanjing Medical University, Nanjing, China.
Jin LiJiangsu Key Laboratory of Oral Disease, Nanjing Medical University, Nanjing, China.
Zhongwu LiJiangsu Key Laboratory of Oral Disease, Nanjing Medical University, Nanjing, China.
Jianrong YangDepartment of Oral and Maxillofacial Surgery, Affiliated Stomatological Hospital, Nanjing Medical University, Nanjing, China.
Yanling WangJiangsu Key Laboratory of Oral Disease, Nanjing Medical University, Nanjing, China.
Jie ChengJiangsu Key Laboratory of Oral Disease, Nanjing Medical University, Nanjing, China.ORCID 0000-0001-9068-4271
Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The long noncoding RNAs (lncRNAs) have been increasingly appreciated as key players underlying tumourigenesis and hold great potentials as prognostic biomarkers and therapeutic targets. However, their roles in head neck squamous cell carcinoma (HNSCC) have remained incompletely known. Here, we sought to reveal the oncogenic roles and clinical significance of a tumour-associated lncRNA, zinc finger E-box binding homeobox 2 antisense RNA 1 (ZEB2-AS1), in HNSCC. ZEB2-AS1 was aberrantly overexpressed in a fraction of HNSCC samples. Its overexpression significantly associated with large tumour size, cervical node metastasis and reduced overall and disease-free survival. Antisense oligonucleotides (ASO)-mediated ZEB2-AS1 depletion markedly inhibited cell proliferation, migration and invasion while triggered apoptosis in HNSCC cells in part via modulating ZEB2 mRNA stability. Enforced overexpression of ZEB2 largely attenuated the phenotypic changes resulted from ZEB2-AS1 inhibition except the impaired cell proliferation. In addition, ZEB2-AS1 was required for TGF-β1-induced epithelial-mesenchymal transition (EMT) in vitro. Significantly reduced tumour growth and lung metastasis were observed in ZEB2-AS1-depleted cells in HNSCC xenograft animal models. Taken together, our findings reveal that overexpression of ZEB2-AS1 associates with tumour aggressiveness and unfavourable prognosis by serving as a putative oncogenic lncRNA and a novel prognostic biomarker in HNSCC.

Indexed as

Epithelial-Mesenchymal TransitionRNA StabilityAdultAgedAged, 80 and overAnimalsApoptosisBiomarkers, TumorCell MovementCell ProliferationFemaleFollow-Up StudiesGene Expression Regulation, NeoplasticHead and Neck NeoplasmsHumansMaleBiomarkers, TumorOligonucleotides, AntisenseRNA, MessengerZEB2 protein, humanZinc Finger E-box Binding Homeobox 2EMThead neck squamous cell carcinomalong noncoding RNAZEB2ZEB2-AS1

Identifiers

PMID30950191
PMCPMC6533490
OpenAlexW2929375473

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.