Evidence map›Paper›PMID 41042406›Full record

ArticleDiscover oncology2025

LncRNA VIM-AS1 is a potential prognostic biomarker and effects on tumor cellular behaviors in breast cancer via impairing miR-29a-3p.

Yang Yuan, Meng Wei, Linna Kong, Pengfei Li, Huihui Zhang, Wenqing Bian, Qun Yuan

Abstract read
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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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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Yang Yuan *Breast Center, The Fourth Hospital of Hebei Medical University, Shijiazhuang, 050035, China.
Meng Wei *Department of Breast Surgery, Chongqing Changshou District Maternal and Child Health Hospital, Chongqing, 401220, China.
Linna KongDepartment of Breast and Thyroid Surgery, Zibo Central Hospital, 54 Gongqingtuan West Road, Zibo, 255020, China.
Pengfei LiDepartment of Breast and Thyroid Surgery, Zibo Central Hospital, 54 Gongqingtuan West Road, Zibo, 255020, China.
Huihui ZhangDepartment of Breast and Thyroid Surgery, Zibo Central Hospital, 54 Gongqingtuan West Road, Zibo, 255020, China.
Wenqing BianDepartment of Breast and Thyroid Surgery, Zibo Central Hospital, 54 Gongqingtuan West Road, Zibo, 255020, China. Bianwenqing_zb@163.com.
Qun YuanDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, No.150, Haping Road, Nangang District, Harbin, 150000, China. YuanquanMD@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe purpose of our research was to investigate the clinical significance of lncRNA VIM anti-sense 1 (VIM-AS1) and to elucidate its cellular functions in breast cancer patients.

methodsA cohort of one hundred and twenty-one individuals diagnosed with breast cancer and 95 healthy volunteers were recruited for this study. Relative abundances of VIM-AS1 were detected through quantitative real-time polymerase chain reaction (qRT-PCR). Receiver operating characteristic (ROC) was employed for evaluating the diagnosis potential of VIM-AS1. Kaplan-Meier method and Cox regression analysis was performed to further examine the prognostic performance of VIM-AS1. The cellular events of VIM-AS1 were assessed via CCK-8 and Transwell assay. The target interaction of VIM-AS1 and microRNA-29a-3p (miR-29a-3p) was verified via luciferase activity report assays.

resultsVIM-AS1 expression was notably elevated in serum of breast cancer, demonstrating a significant diagnostic capacity for breast cancer patients. Its abnormal expression level was significantly correlated with TNM (tumor node metastasis, P = 0.020) and lymph node metastasis (P = 0.040). Moreover, a reduced overall survival rate was observed in patients exhibiting high VIM-AS1 expression (P = 0.001). Multivariate analysis illustrated that VIM-AS1 (P = 0.003, HR = 2.345, 95%CI = 1.340-4.103) was an independent prognostic biomarker for breast cancer patients, alongside TNM (P = 0.006; HR = 2.251; 95%CI = 1.24-4.009). Functionally, silencing VIM-AS1 resulted in the inhibition of key cell behaviors in vitro, including proliferation, migration and invasion. Besides, VIM-AS1 was found to negatively regulated miR-29a-3p, which may relieve the impacts of VIM-AS1 on breast cancer cells.

conclusionVIM-AS1 exhibited aberrant expression in breast cancer, playing a critical role in tumor development by targeting miR-29a-3p. Our findings highlight the potential of VIM-AS1 as a novel diagnostic and prognostic biomarker in breast cancer. However, further in vivo studies and exploration of miR-29a-3p downstream targets are needed to fully elucidate the mechanistic role of VIM-AS1 in breast cancer progression.

Indexed as

Breast cancerMiR-29a-3pPrognosisVIM-AS1

Identifiers

PMID41042406
PMCPMC12495003

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