Evidence map›Paper›PMID 30515972›Full record

ArticleJournal of cellular and molecular medicine2019

LncRNA DUXAP9-206 directly binds with Cbl-b to augment EGFR signaling and promotes non-small cell lung cancer progression.

Ting Zhu, Shu An, Man-Ting Choy, Junhao Zhou, Shanshan Wu, Shihua Liu, Bangdong Liu, Zhicheng Yao, Xun Zhu, Jueheng Wu and 1 more

Erratum issuedOpen 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. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.6field-weighted citation impact, top 36% 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, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. LncRNA AL645608.3 mediates malignant progression of acute myeloid leukemia.American journal of translational research · 2024
    Article
  5. Article
  6. Review
  7. The Role of Long Noncoding RNA (lncRNAs) Biomarkers in Renal Cell Carcinoma.International journal of molecular sciences · 2022
    Review
  8. Journal of cellular and molecular medicine · 2022
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
4 · The record

Corrections and comments

  • Erratum issued
    2022
5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Ting ZhuSchool of Public Health, Sun Yat-sen University, Guangzhou, China.
Shu AnDepartment of Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Man-Ting ChoyDepartment of Endocrinology, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Junhao ZhouDepartment of Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Shanshan WuDepartment of Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Shihua LiuDepartment of Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Bangdong LiuDepartment of Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Zhicheng YaoDepartment of General Surgery, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China.
Xun ZhuDepartment of Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Jueheng WuDepartment of Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
Zhenjian HeSchool of Public Health, Sun Yat-sen University, Guangzhou, China.ORCID 0000-0002-9026-8232
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) are involved in the pathology of various tumours, including non-small cell lung cancer (NSCLC). However, the underlying molecular mechanisms of their specific association with NSCLC have not been fully elucidated. Here, we report that a cytoplasmic lncRNA, DUXAP9-206 is overexpressed in NSCLC cells and closely related to NSCLC clinical features and poor patient survival. We reveal that DUXAP9-206 induced NSCLC cell proliferation and metastasis by directly interacting with Cbl-b, an E3 ubiquitin ligase, and reducing the degradation of epidermal growth factor receptor (EGFR) and thereby augmenting EGFR signaling in NSCLC. Notably, correlations between DUXAP9-206 and activated EGFR signaling were also validated in NSCLC patient specimens. Collectively, our findings reveal the novel molecular mechanisms of DUXAP9-206 in mediating the progression of NSCLC and DUXAP9-206 may serve as a potential target for NSCLC therapy.

Indexed as

Gene Expression Regulation, NeoplasticAdaptor Proteins, Signal TransducingAnimalsApoptosisBiomarkers, TumorCarcinoma, Non-Small-Cell LungCell MovementCell ProliferationErbB ReceptorsFemaleHumansLung NeoplasmsMiceMice, Inbred BALB CMice, NudePrognosisAdaptor Proteins, Signal TransducingBiomarkers, TumorCBLB protein, humanEGFR protein, humanErbB ReceptorsProto-Oncogene Proteins c-cblRNA, Long NoncodingCbl-bDUXAP9-206EGFR signalinglncRNAnon-small cell lung cancer

Identifiers

PMID30515972
PMCPMC6378200
OpenAlexW2902333082

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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.