Evidence map›Paper›PMID 38726776›Full record

ArticleCurrent pharmaceutical biotechnology2025

LncRNA LINC00466 Promotes the Progression of Breast Cancer

Xue Han, Fan Shi, Shujun Guo, Yao Li, Hongtao Wang, Chuanwang Song, Shiwu Wu

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Article in Current pharmaceutical biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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

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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

2 citing papers in PubMed.

  1. Article
  2. Epigenomics · 2024
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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

7 authors.

Xue HanDepartment of Immunology, School of Laboratory Medicine, Bengbu Medical University, Bengbu, 233030, China.
Fan ShiDepartment of Pathology, the First Affiliated Hospital of Bengbu Medical University, Bengbu, 233004,China.
Shujun GuoDepartment of Immunology, School of Laboratory Medicine, Bengbu Medical University, Bengbu, 233030, China.
Yao LiDepartment of Immunology, School of Laboratory Medicine, Bengbu Medical University, Bengbu, 233030, China.
Hongtao WangDepartment of Immunology, School of Laboratory Medicine, Bengbu Medical University, Bengbu, 233030, China.
Chuanwang SongDepartment of Immunology, School of Laboratory Medicine, Bengbu Medical University, Bengbu, 233030, China.
Shiwu WuDepartment of Pathology, the First Affiliated Hospital of Bengbu Medical University, Bengbu, 233004,China.

Funding

Anhui Provincial College Students Innovation and Entrepreneurship Project S202010367101Anhui Provincial Natural Science Foundation 2008085QH410College Students Innovation and Entrepreneurship Project of Bengbu Medical College bydc2022030Key Project of Natural Science Research in Higher Education Institutions of Anhui Province KJ2021A0725Major University Science Research Project of Anhui Province KJ2020ZD49Natural Science Research Program of Bengbu Medical College BYKY1804ZD, 2020bypd009
6 · The paper itself

Abstract

backgroundBreast Cancer (BC) is a female malignancy with a high mortality rate. Novel diagnostic and prognostic biomarkers are valuable for reducing BC mortality. Our study is designed to undrape the precise role of the LINC00466/miR-4731-5p/EPHA2 axis in BC.

methodsThe Cancer Genome Atlas (TCGA) sequencing dataset was utilized to compare the levels of LINC00466. The levels of LINC00466, miR-4731-5p, and EPHA2 were tested by qRTPCR. Cell proliferation and cycle were detected by CCK-8 assay and flow cytometer.

resultsLINC00466 was increased in human breast cancer tissues. LINC00466 was negatively associated with miR-4731-5p and positively correlated with EPHA2 in human breast cancer tissues. Down-regulation of LINC00466 suppressed the proliferation and arrested the cell cycle of breast cancer cells, and inhibited tumor growth

conclusionLINC00466 promoted BC development via mediating the miR-4731-5p/EPHA2 axis, which has the potential value as a promising therapeutic target in BC.

Indexed as

Breast NeoplasmsCell ProliferationMice, NudeMicroRNAsReceptor, EphA2RNA, Long NoncodingAnimalsCell Line, TumorDisease ProgressionFemaleGene Expression Regulation, NeoplasticHumansMiceMice, Inbred BALB CEPHA2 protein, humanMicroRNAsReceptor, EphA2RNA, Long Noncodingbiomarkers.Breast cancerEPHA2LINC00466miR-4731-5pXenograft nude models

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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.