Evidence map›Paper›PMID 31686834›Full record

ArticleOncoTargets and therapy2019

Linc00467 promotes lung adenocarcinoma proliferation via sponging miR-20b-5p to activate CCND1 expression.

Hao Ding, Yuchuan Luo, Ke Hu, Pei Liu, Mengqing Xiong

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. LINC00467 mediates the 5-fluorouracil resistance in breast cancer cells.In vitro cellular & developmental biology. Animal · 2024
    Article
  5. Review
  6. Article
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  9. Review
  10. LINC00467: an oncogenic long noncoding RNA.Cancer cell international · 2022
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
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  17. LncRNA Lnc-APUE is Repressed by HNF4Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Article
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  19. 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

5 authors at 2 institutions in 1 country.

Hao DingDivision of Respiratory Disease, Renmin Hospital of Wuhan University, Wuhan, People's Republic of China.
Yuchuan LuoDivision of Respiratory Disease, Renmin Hospital of Wuhan University, Wuhan, People's Republic of China.
Ke HuDivision of Respiratory Disease, Renmin Hospital of Wuhan University, Wuhan, People's Republic of China.
Pei LiuDivision of Respiratory Disease, Renmin Hospital of Wuhan University, Wuhan, People's Republic of China.
Mengqing XiongDivision of Respiratory Disease, Renmin Hospital of Wuhan University, Wuhan, People's Republic of China.
Wuhan University · CNRenmin Hospital of Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecently, numerous studies have demonstrated the emerging role of long non-coding RNAs (lncRNAs) in human cancers. Linc00467 is a newly defined lncRNA and was reported to promote cell survival in neuroblastoma. However, the function of linc00467 in lung cancer is still unclear. MATERIAL AND

methodsWe analyzed linc00467 expression and survival data derived from The Cancer Genome Altas lung adenocarcinoma (LUAD) dataset as well as in collected LUAD tissues. Then, we silenced linc00467 expression in two lung cancer cell lines using small interfering RNAs and explored the effect of linc00467 knockdown on cell growth in vitro and in vivo. Moreover, we revealed a novel target gene of linc00467 and elucidated the underlying competitive endogenous RNA regulatory mechanism in lung cancer cells.

resultsOur data suggested that linc00467 expression was elevated in LUAD tissues and correlated with overall survival of LUAD patients. Linc00467 knockdown resulted in reduced proliferation rate in lung cancer cells. Furthermore, we elucidated that linc00467 promoted CCND1 expression in lung cancer cells via functioning as a molecular sponge for miR-20b-5p.

conclusionLinc00467/miR-20b-5p/CCND1 signaling pathway may provide new insights into lung cancer treatment.

Indexed as

CCND1cell growthlinc00467lung adenocarcinomamiR-20b-5p

Identifiers

PMID31686834
PMCPMC6709798
OpenAlexW2969907661

What OpenQuestion holds

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Registered trials

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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.