Evidence map›Paper›PMID 32149330›Full record

Observational studyBioscience reports2020

LncRNA XIST promotes the progression of laryngeal squamous cell carcinoma via sponging miR-125b-5p to modulate TRIB2.

Chunxiu Liu, Zhenjun Lu, Hui Liu, Shenfa Zhuang, Ping Guo

RetractedOpen access · goldAbstract readObservational StudyRetracted Publication
In one paragraph

Observational study in Bioscience reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Long non-coding RNA XIST: a novel oncogene in multiple cancers.Molecular medicine (Cambridge, Mass.) · 2021
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Biological Function of Long Non-coding RNA (LncRNA) Xist.Frontiers in cell and developmental biology · 2021
    Review
  14. Article
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Chunxiu LiuDepartment of Otolaryngology, Jining First People's Hospital of Shandong Province, Jining, Shandong, China.
Zhenjun LuDepartment of Otolaryngology, The Third People's Hospital, Qingdao, Shandong, China.
Hui LiuDepartment of Otolaryngology, Jining First People's Hospital of Shandong Province, Jining, Shandong, China.
Shenfa ZhuangDepartment of Otolaryngology, Jining First People's Hospital of Shandong Province, Jining, Shandong, China.
Ping GuoDepartment of Otolaryngology, Jining First People's Hospital of Shandong Province, Jining, Shandong, China.
Jining First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveX inactivate-specific transcript (XIST) is an attractive long noncoding RNA (lncRNA) functioning as an indicator of various human tumors, including laryngeal squamous cell carcinoma (LSCC). The present study was conducted to explore a novel regulatory network of lncRNA XIST in LSCC cells. MATERIALS AND

methodsQuantitative real-time polymerase chain reaction (QRT-PCR) was used to detect the expression levels of XIST, miR-125b-5p and TRIB2 in LSCC cells and tissues. Cell proliferation, apoptosis, migration and invasion were detected by Cell Counting Kit-8 (CCK-8), flow cytometry and Transwell assays, separately. The relationship among XIST, miR-125b-5p and tribbles homolog 2 (TRIB2) was predicted by starBase v2.0 or TargetScan and confirmed by Dual-luciferase reporter assay. The TRIB2 protein expression was quantified by Western blot assay. Murine xenograft model was utilized to validate the role of XIST in vivo.

resultsXIST was notably up-regulated in LSCC tissues and cells, and the high level of XIST was associated with the low survival rate of LSCC patients. XIST knockdown markedly repressed cell proliferation, migration and invasion and promoted the apoptosis of LSCC cells and the effects were antagonized by loss of miR-125b-5p. MiR-125b-5p was a target of XIST in LSCC cells, and it could bind to TRIB2 as well. Moreover, XIST-loss-induced down-regulation of TRIB2 could be significantly reversed by miR-125b-5p knockdown. XIST promoted the growth of LSCC tumor in vivo.

conclusionLncRNA XIST promoted the malignance of LSCC cells partly through competitively binding to miR-125b-5p, which in turn increased TRIB2 expression.

Indexed as

AnimalsCalcium-Calmodulin-Dependent Protein KinasesDisease ProgressionFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansLaryngeal NeoplasmsLaryngectomyLarynxMaleMiceMicroRNAsMiddle AgedRNA, Long NoncodingSquamous Cell Carcinoma of Head and NeckCalcium-Calmodulin-Dependent Protein KinasesMicroRNAsMIRN125 microRNA, humanRNA, Long NoncodingTRIB2 protein, humanXIST non-coding RNAlaryngeal squamous cell carcinomaLncRNA XISTmiR-125b-5pTRIB2

Identifiers

PMID32149330
PMCPMC7146034
OpenAlexW3012508263

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.