Evidence map›Paper›PMID 41467969›Full record

ArticleDiscover oncology2025

microRNA-1258 suppresses breast cancer progression by targeting LARP4B.

Jianping Lai, Liang An, Yongqing Zhang, Xinbo Wang

Abstract read
In one paragraph

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

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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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

4 authors.

Jianping Lai *Department of Radiation Oncology for Thoracic Tumors, Ganzhou Cancer Hospital, Ganzhou, 341000, China.
Liang An *Department of Surgical Oncology, Shanghai Mengchao Tumor Hospital, Shanghai, 200000, China.
Yongqing ZhangDepartment of Breast and Thyroid Surgery, Weifang People's Hospital, 151 Guangwen Street, Kuiwen District, Weifang, 261000, China.
Xinbo WangDepartment of Breast and Thyroid Surgery, Weifang People's Hospital, 151 Guangwen Street, Kuiwen District, Weifang, 261000, China. wxbshandong123@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer (BC) is the most common cancer in women. The majority of BC-related deaths result from metastasis and invasion. MicroRNA (miRNA) is a key regulatory factor that suppresses the expression of target genes. miR-1258 is considered one of the miRNAs significantly associated with BC, but its downstream target genes have not been fully defined. Our study aimed to elucidate the role of miR-1258 in breast cancer cell proliferation, migration, and invasion, identify its potential targets, and investigate its regulatory mechanisms.

methodsmiR-1258 expression in breast cancer was measured by Real‑time quantitative PCR. The effects of the Cell Counting Kit-8 method, the Transwell migration and invasion method on the behavior of tumor-related cells were studied. In addition, the interaction between miR-1258 and LARP4B in cancer was elucidated using dual-luciferase assays and Pearson correlation analysis.

resultsmiR-1258 is significantly downregulated in breast cancer, whereas LARP4B is significantly upregulated; both are closely associated with patients’ TNM staging. miR-1258 is an independent prognostic factor; patients with low expression of miR-1258 exhibit shorter overall survival. In BC cells, overexpression of miR-1258 inhibits cell proliferation, migration, and invasion. LARP4B is a potential target gene of miR-1258, and silencing LARP4B inhibits cellular biological functions.

conclusionsLow expression of miR-1258 may indicate poor prognosis in BC whilst its overexpression significantly inhibits proliferation, migration and invasion of BC cells. miR-1258 may inhibit BC progression by negatively regulating LARP4B.

Indexed as

Breast cancerLa-Related protein 4BMiR-1258MiRNAs

Identifiers

PMID41467969
PMCPMC12858697

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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.