Evidence map›Paper›PMID 26261546›Full record

ArticleInternational journal of clinical and experimental pathology2015

MiR-1228 promotes breast cancer cell growth and metastasis through targeting SCAI protein.

Luoqiang Lin, Dan Liu, Hongyan Liang, Li Xue, Changlei Su, Ming Liu

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

28 citing papers in PubMed, 43 citations in OpenAlex.

  1. Microrna Expression inMicroRNA (Shariqah, United Arab Emirates) · 2026
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  4. International journal of molecular sciences · 2024
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  11. Observational
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Exosomal MiRNAs in Pediatric Cancers.International journal of molecular sciences · 2019
    Review
  19. Article
  20. MiRNA-134 suppresses esophageal squamous cell carcinoma progression by targeting FOXM1.International journal of clinical and experimental pathology · 2019
    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

6 authors at 1 institution in 1 country.

Luoqiang LinDepartment of General Surgery, The Fourth Affiliated Hospital of Harbin Medical University Harbin 150010, China.
Dan LiuDepartment of 7th Oncology, The Third Affiliated Hospital of Harbin Medical University Harbin 150086, China.
Hongyan LiangDepartment of General Surgery, The Fourth Affiliated Hospital of Harbin Medical University Harbin 150010, China.
Li XueDepartment of General Surgery, The Fourth Affiliated Hospital of Harbin Medical University Harbin 150010, China.
Changlei SuDepartment of The Third General Surgery, The Second Affiliated Hospital of Harbin Medical University Harbin 150086, China.
Ming LiuDepartment of General Surgery, The Fourth Affiliated Hospital of Harbin Medical University Harbin 150010, China.
Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is the most common cancer in women around the world. However, the molecular mechanisms underlying breast cancer pathogenesis are only partially understood. Here, in this study, we found that miR-1228 was up-regulated in breast cancer cell lines and tissues. Ectopic expression of miR-1228 mimics leads to promoted cell growth, invasion and migration. Using bioinfomatic analysis and 3'UTR luciferase reporter assay, we determined SCAI can be directly targeted by miR-1228, which can down-regulate endogenous SCAI protein level. Furthermore, our findings demonstrate that SCAI was down-regulated in breast cancer cell lines and tissues. Rescue experiment demonstrated that miR-1228 promoted cell growth is attenuated by over-expression of MOAP1 and miR-1228 promoted cell invasion and migration can be attenuated by over-expression of SCAI. Taken together, this study provides evidences that miR-1228 serves as an oncogene to promote breast cancer proliferation, invasion and migration, which may become a critical therapeutic target for breast cancer treatment.

Indexed as

Cell MovementCell Proliferation3' Untranslated RegionsAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsBinding SitesBreast NeoplasmsComputational BiologyFemaleGene Expression Regulation, NeoplasticGenes, ReporterHumansMCF-7 CellsMicroRNAsNeoplasm InvasivenessSignal Transduction3' Untranslated RegionsAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsMicroRNAsMIRN1228 microRNA, humanMOAP1 protein, humanSCAI protein, humanTranscription FactorsBreast cancercell invasioncell migrationcell proliferationmiR-1228SCAI

Identifiers

PMID26261546
PMCPMC4525880
OpenAlexW1425666771

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.