Evidence map›Paper›PMID 33311496›Full record

ArticleCell death & disease2020

LINC01106 post-transcriptionally regulates ELK3 and HOXD8 to promote bladder cancer progression.

Liwei Meng, Zhaoquan Xing, Zhaoxin Guo, Zhaoxu Liu

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-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, 42 citations in OpenAlex.

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  18. [Expression characteristics and functional analysis of ELK3 in gastric cancer].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2021
    Article
  19. Article
  20. Promising Advances in LINC01116 Related to Cancer.Frontiers in cell and developmental biology · 2021
    Review
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

4 authors at 1 institution in 1 country.

Liwei MengQilu Hospital of Shandong University, Jinan, 250000, Shandong Province, China.
Zhaoquan XingQilu Hospital of Shandong University, Jinan, 250000, Shandong Province, China.
Zhaoxin GuoQilu Hospital of Shandong University, Jinan, 250000, Shandong Province, China.
Zhaoxu LiuQilu Hospital of Shandong University, Jinan, 250000, Shandong Province, China. zhaoxvl@sdu.edu.cn.
Qilu Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bladder cancer (BCa) is a kind of common urogenital malignancy worldwide. Emerging evidence indicated that long noncoding RNAs (lncRNAs) play critical roles in the progression of BCa. In this study, we discovered a novel lncRNA LINC01116 whose expression increased with stages in BCa patients and closely related to the survival rate of BCa patients. However, the molecular mechanism dictating the role of LINC01116 in BCa has not been well elucidated so far. In our study, we detected that the expression of LINC01116 was boosted in BCa cells. Moreover, the results of a series of functional assays showed that LINC01116 knockdown suppressed the proliferation, migration, and invasion of BCa cells. Thereafter, GEPIA indicated the closest correlation of LINC01116 with two protein-coding genes, ELK3 and HOXD8. Interestingly, LINC01116 was mainly a cytoplasmic lncRNA in BCa cells, and it could modulate ELK3 and HOXD8 at post-transcriptional level. Mechanically, LINC01116 increased the expression of ELK3 by adsorbing miR-3612, and also stabilized HOXD8 mRNA by binding with DKC1. Rescue experiments further demonstrated that the restraining influence of LINC01116 knockdown on the progression of BCa, was partly rescued by ELK3 promotion, but absolutely reversed by the co-enhancement of ELK3 and HOXD8. More intriguingly, HOXD8 acted as a transcription factor to activate LINC01116 in BCa. In conclusion, HOXD8-enhanced LINC01116 contributes to the progression of BCa via targeting ELK3 and HOXD8, which might provide new targets for treating patients with BCa.

Indexed as

Disease ProgressionGene Expression Regulation, NeoplasticTranscription, GeneticAnimalsBase SequenceCell Cycle ProteinsCell Line, TumorCell MovementCell ProliferationEpithelial-Mesenchymal TransitionGene Knockdown TechniquesHomeodomain ProteinsHumansMaleMice, Inbred BALB CMice, NudeCell Cycle ProteinsDKC1 protein, humanElk3 protein, humanHomeodomain ProteinsHOXD8 protein, humanMicroRNAsMIRN3612 microRNA, humanNuclear ProteinsProto-Oncogene Proteins c-etsRNA, Long NoncodingTranscription Factors

Identifiers

PMID33311496
PMCPMC7733594
OpenAlexW3116502777

What OpenQuestion holds

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LicenceCC BY
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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.