Evidence map›Paper›PMID 40673312›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2025

[LncRNA SNHG15 promotes proliferation, migration and invasion of lung adenocarcinoma cells by regulating COX6B1 through sponge adsorption of miR-30b-3p].

Xiuying Gong, Shunfu Hou, Miaomiao Zhao, Xiaona Wang, Zhihan Zhang, Qinghua Liu, Chonggao Yin, Hongli Li

Abstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Xiuying GongSchool of Basic Medical Sciences, Shandong Second Medical University, Weifang 261000, China.
Shunfu HouSchool of Basic Medical Sciences, Shandong Second Medical University, Weifang 261000, China.
Miaomiao ZhaoSchool of Basic Medical Sciences, Shandong Second Medical University, Weifang 261000, China.
Xiaona WangSchool of Basic Medical Sciences, Shandong Second Medical University, Weifang 261000, China.
Zhihan ZhangSchool of Life Sciences and Technology, Shandong Second Medical University, Weifang 261000, China.
Qinghua LiuSchool of Basic Medical Sciences, Shandong Second Medical University, Weifang 261000, China.
Chonggao YinSchool of Nursing, Shandong Second Medical University, Weifang 261000, China.
Hongli LiSchool of Basic Medical Sciences, Shandong Second Medical University, Weifang 261000, China.

Funding

National Natural Science Foundation of China 82373043
6 · The paper itself

Abstract

objectivesTo explore the molecular mechanism by which lncRNA SNHG15 regulates proliferation, invasion and migration of lung adenocarcinoma cells.

methodsThe lncRNA microarray chip dataset GSE196584 and LncBase were used to predict the lncRNAs that interact with miR-30b-3p, and their association with patient prognosis were investigated using online databases, after which lncRNA nucleolar RNA host gene 15 (SNHG15) was selected for further analysis. The subcellular localization of lncRNA SNHG15 and its expression levels in normal human lung epithelial cells and lung adenocarcinoma cell lines were detected using fluorescence in situ hybridization and qRT-PCR. In cultured A549 cells, the changes in cell proliferation, migration, and invasion following transfection with a SNHG15 knockdown plasmid (sh-SNHG15), a miR-30b-3p inhibitor, or their co-transfection were assessed with EdU, wound healing, and Transwell assays. Bioinformatics analyses were used to predict the regulatory relationship between lncRNA SNHG15 and COX6B1, and the results were verified using Western blotting and rescue experiments in A549 cells transfected with sh-SNHG15, a COX6B1-overexpressing plasmid, or both.

resultsLncRNA SNHG15 was shown to target miR-30b-3p, and the former was highly expressed in lung adenocarcinoma, and associated with a poor patient prognosis. LncRNA SNHG15 was localized in the cytoplasm and expressed at higher levels in A549 and NCI-H1299 cells than in BEAS-2B cells. In A549 cells, lncRNA SNHG15 knockdown significantly inhibited cell migration, invasion and proliferation, and these changes were reversed by miR-30b-3p inhibitor. A regulatory relationship was found between lncRNA SNHG15 and COX6B1, and their expression levels were positively correlated (

conclusionsLncRNA SNHG15 may compete with COX6B1 to bind miR-30b-3p through a ceRNA mechanism to affect proliferation, migration, and invasion of lung adenocarcinoma cells.

Indexed as

AdenocarcinomaLung NeoplasmsMicroRNAsRNA, Long NoncodingA549 CellsAdenocarcinoma of LungCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHumansNeoplasm InvasivenessMicroRNAsMIRN30b microRNA, humanRNA, Long NoncodingCOX6B1invasionlong non-coding RNA SNHG15lung adenocarcinomamigrationmiR-30b-3p

Identifiers

PMID40673312
PMCPMC12268920

What OpenQuestion holds

Textmetadata
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.