Evidence map›Paper›PMID 31297902›Full record

ArticleCell proliferation2019

Long non-coding RNA HOTAIR/microRNA-206 sponge regulates STC2 and further influences cell biological functions in head and neck squamous cell carcinoma.

Tiancheng Li, Yao Qin, Zhen Zhen, Hong Shen, Tiechuan Cong, Erik Schiferle, Shuifang Xiao

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cell proliferation, 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 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

42 citing papers in PubMed, 62 citations in OpenAlex.

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  18. Stanniocalcin 2 (STC2): a universal tumour biomarker and a potential therapeutical target.Journal of experimental & clinical cancer research : CR · 2022
    Review
  19. Review
  20. Corrigendum.Cell proliferation · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Tiancheng LiDepartment of Otorhinolaryngology-Head and Neck Surgery, Peking University First Hospital, Beijing, China.
Yao QinDepartment of Otorhinolaryngology-Head and Neck Surgery, Peking University First Hospital, Beijing, China.
Zhen ZhenDepartment of Otorhinolaryngology-Head and Neck Surgery, Peking University First Hospital, Beijing, China.
Hong ShenDepartment of Otorhinolaryngology-Head and Neck Surgery, Peking University First Hospital, Beijing, China.
Tiechuan CongDepartment of Otorhinolaryngology-Head and Neck Surgery, Peking University First Hospital, Beijing, China.
Erik SchiferleCenter for Cancer Research, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Shuifang XiaoDepartment of Otorhinolaryngology-Head and Neck Surgery, Peking University First Hospital, Beijing, China.ORCID https://orcid.org/0000-0001-6133-2293
Peking University · CNHarvard University · US

Funding

Beijing Xisike Clinical Oncology Research Foundation Y-MT2016-014
6 · The paper itself

Abstract

objectiveIt is essential to characterize underlying molecular mechanism associated with head and neck squamous cell carcinoma (HNSCC) and identify promising therapeutic targets. Herein, we explored role of homeobox transcript antisense RNA (HOTAIR) in HNSCC to regulate stanniocalcin-2 (STC2) by sponging microRNA-206 (miR-206).

methodsHNSCC-related differentially expressed genes and regulation network amongst HOTAIR, miR-206 and STC2 were identified. Next, effect of HOTAIR on cell biological functions of HNSCC was identified after transfection of cells with HOTAIR overexpressed plasmids or siRNA against HOTAIR. PI3K/AKT signalling pathway-related gene expression was measured after miR-206 and STC2 were suppressed. Cell invasion, migration and proliferation were assessed. Finally, tumour growth was assessed to determine the effects of HOTAIR/miR-206/STC2 axis in vivo.

resultsHOTAIR specifically bound to miR-206 and miR-206 targeted STC2. Downregulated HOTAIR or upregulated miR-206 suppressed HNSCC cell proliferation, invasion and migration. miR-206 inhibited PI3K/AKT signalling pathway by down-regulating STC2. Besides, silenced HOTAIR or overexpressed miR-206 repressed the tumour growth of nude mice with HNSCC.

conclusionHOTAIR regulated HNSCC cell biological functions by binding to miR-206 through STC2.

Indexed as

AnimalsApoptosisCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticGlycoproteinsHead and Neck NeoplasmsHumansIntercellular Signaling Peptides and ProteinsMiceMice, NudeMicroRNAsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktGlycoproteinsHOTAIR long untranslated RNA, humanIntercellular Signaling Peptides and ProteinsMicroRNAsMIRN206 microRNA, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRNA, Long NoncodingRNA, Small InterferingSTC2 protein, humanhead and neck squamous cell carcinomainvasionlong non-coding RNA homeobox transcript antisense RNAmicroRNA-206migrationproliferationstanniocalcin-2

Identifiers

PMID31297902
PMCPMC6797510
OpenAlexW2960075396

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.