Evidence map›Paper›PMID 35332412›Full record

ArticleMolecular biology reports2022

LncRNA BACE1-AS promotes the progression of osteosarcoma through miR-762/SOX7 axis.

Chunlei Wang, Tao Zhang, Lin Yang, Xinyu Na, Yanlong Qu

Abstract read
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In one paragraph

Article in Molecular biology reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. LncRNA BACE1-AS delays the propagation ofMicrobiology spectrum · 2025
    Article
  3. Apelin/APJ: Another Player in the Cancer Biology Network.International journal of molecular sciences · 2025
    Review
  4. Article
  5. Review
  6. 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

5 authors at 1 institution in 1 country.

Chunlei WangThe Third Department of Orthopedic, The First Affiliate Hospital of Harbin Medical University, Youzheng Street, Nangang District, Harbin, 150001, Heilongjiang, China.
Tao ZhangThe Third Department of Orthopedic, The First Affiliate Hospital of Harbin Medical University, Youzheng Street, Nangang District, Harbin, 150001, Heilongjiang, China.
Lin YangThe Third Department of Orthopedic, The First Affiliate Hospital of Harbin Medical University, Youzheng Street, Nangang District, Harbin, 150001, Heilongjiang, China.
Xinyu NaThe Third Department of Orthopedic, The First Affiliate Hospital of Harbin Medical University, Youzheng Street, Nangang District, Harbin, 150001, Heilongjiang, China.
Yanlong QuThe Third Department of Orthopedic, The First Affiliate Hospital of Harbin Medical University, Youzheng Street, Nangang District, Harbin, 150001, Heilongjiang, China. quyanlong16@sina.com.ORCID http://orcid.org/0000-0002-5576-269X
Harbin Medical University · CN

Funding

Scientific Research Foundation of Graduate School of Harbin Medical University: Sino Russian Special Fund C2020186
6 · The paper itself

Abstract

backgroundOsteosarcoma (OS) is a rare malignant primary tumor of mesenchymal origin affecting bone that occurs in adolescents and children. LncRNAs are important regulators of tumorigenesis and development. This study aimed to explore the role and molecular basis of LncRNA BACE1-AS (BACE1 antisense RNA) in OS. METHODS AND

resultsThrough the analysis of differential expressed lncRNAs in OS tissues by GEO database, LncRNA BACE1-AS display a remarkably lower expression. This found can also be observed in both OS tissues and cell lines by qRT-PCR. Furthermore, using Cell counting kit-8 (CCK-8), transwell, wound healing and westernblot assays, overexpression LncRNA BACE1-AS remarkably reduce cell proliferation, migration and invasion abilities in OS. In addition, LncRNA BACE1-AS is validated as a sponge of miR-762 through the prediction of lncRNASNP. Further, luciferase reporter and RIP assays are conducted to confirm the binding sites between LncRNA BACE1-AS and miR-762. SRY-box transcription factor 7 (SOX7) target to miR-762 and regulated by LncRNA BACE1-AS. Moreover, inhibition of miR-762 attenuate the role of sh-LncRNA BACE1-AS in OS cells, at meanwhile reduce the expression of SOX7.

conclusionIn this study, LncRNA BACE1-AS regulates proliferation, migration and invasion of osteosarcoma cells by miR-762/SOX7 axis, implying that LncRNA BACE1-AS is a potential target for osteosarcoma therapy.

Indexed as

Bone NeoplasmsMicroRNAsOsteosarcomaRNA, Long NoncodingAdolescentAmyloid Precursor Protein SecretasesAspartic Acid EndopeptidasesCell Line, TumorCell MovementCell ProliferationChildGene Expression Regulation, NeoplasticHumansSOXF Transcription FactorsAmyloid Precursor Protein SecretasesAspartic Acid EndopeptidasesBACE1 protein, humanMicroRNAsMIRN762 microRNA, humanRNA, Long NoncodingSOX7 protein, humanSOXF Transcription FactorsInvasionLncRNA BACE1-ASmiR-762OsteosarcomaProliferationSOX7

Identifiers

PMID35332412
OpenAlexW4220666131

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.