Evidence map›Paper›PMID 39953309›Full record

ArticleOdontology2025

HNF1A-AS1 promotes oral squamous cell carcinoma progression via regulating miR-138/CDK6 pathway.

Bingxin Mei, Zhimei Zeng, Qinmin Xia, Ming Liu, Li Lei

Abstract read
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In one paragraph

Article in Odontology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Bingxin MeiDepartment of Stomatology, The First Affiliated Hospital Of Gannan Medical University, No.128, Jinling Road, Ganzhou, 341000, Jiangxi, China.
Zhimei ZengDepartment of Stomatology, The First Affiliated Hospital Of Gannan Medical University, No.128, Jinling Road, Ganzhou, 341000, Jiangxi, China.
Qinmin XiaDepartment of Stomatology, The First Affiliated Hospital Of Gannan Medical University, No.128, Jinling Road, Ganzhou, 341000, Jiangxi, China.
Ming LiuDepartment of Stomatology, The First Affiliated Hospital Of Gannan Medical University, No.128, Jinling Road, Ganzhou, 341000, Jiangxi, China.
Li LeiDepartment of Stomatology, The First Affiliated Hospital Of Gannan Medical University, No.128, Jinling Road, Ganzhou, 341000, Jiangxi, China. 15079717000@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The action and the latent mechanism of HNF1A-AS1 in oral squamous cell carcinoma (OSCC) development were probed. Levels of HNF1A-AS1, microRNA-138 (miR-138) and Cyclin-dependent kinase 6 (CDK6) were examined. In vitro assays were conducted using SCC-4 and SCC15 cells derived from a human SCC of the tongue of a 55-year-old male. In vivo assay was performed by establishing OSCC mouse models. An elevated HNF1A-AS1 was detected in OSCC, and down-expressed HNF1A-AS1 inhibited migration and invasion, and promoted apoptosis in OSCC cells in vitro. HNF1A-AS1 targeted miR-138 to positively regulate the expression of CDK6, a target of miR-138. Knockdown of miR-138 attenuated the action of HNF1A-AS1 silencing on OSCC cell malignant phenotypes. Besides that, overexpression of CDK6 weakened miR-138-mediated anti-cancer functions. Moreover, HNF1A-AS1 knockdown restrained OSCC growth in nude mice. HNF1A-AS1 promoted OSCC tumorigenesis via miR-138/CDK6 pathway, indicating the potential molecular contribution of HNF1A-AS1 on OSCC pathogenesis.

Indexed as

Carcinoma, Squamous CellCyclin-Dependent Kinase 6MicroRNAsMouth NeoplasmsAnimalsApoptosisCell Line, TumorCell MovementDisease ProgressionGene Expression Regulation, NeoplasticHumansMaleMiceMice, NudeMiddle AgedNeoplasm InvasivenessCDK6 protein, humanCyclin-Dependent Kinase 6long non-coding RNA HNF1A-AS1, humanMicroRNAsMIRN138 microRNA, humanRNA, Long NoncodingCDK6HNF1A-AS1miR-138OSCCProgression

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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.