Evidence map›Paper›PMID 32458152›Full record

ArticleBreast cancer (Tokyo, Japan)2020

SNORA71B promotes breast cancer cells across blood-brain barrier by inducing epithelial-mesenchymal transition.

Sijia Duan, Xuliang Luo, Huihui Zeng, Xiang Zhan, Chunlei Yuan

Open access · hybridAbstract read
In one paragraph

Article in Breast cancer (Tokyo, Japan), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Biological profile of breast cancer brain metastasis.Acta neuropathologica communications · 2025
    Review
  3. Small nucleolar RNAs: the hidden precursors of cancer ribosomes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  4. Review
  5. Non-Coding RNAs in Breast Cancer: Diagnostic and Therapeutic Implications.International journal of molecular sciences · 2024
    Review
  6. Review
  7. Article
  8. Review
  9. The Journey of Cancer Cells to the Brain: Challenges and Opportunities.International journal of molecular sciences · 2023
    Review
  10. Review
  11. Review
  12. Article
  13. 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 2 institutions in 1 country.

Sijia DuanDepartment of Breast Surgery, The Second Affiliated Hospital of Nanchang University, No.1 Mingde Road, Donghu District, Nanchang, 330006, Jiangxi Province, China.
Xuliang LuoMedical College of Nanchang University, Nanchang, 330006, Jiangxi, People's Republic of China.
Huihui ZengThe People's Hospital of Le 'An County, Fuzhou, 344000, Jiangxi, China.
Xiang ZhanThe People's Hospital of Le 'An County, Fuzhou, 344000, Jiangxi, China.
Chunlei YuanDepartment of Breast Surgery, The Second Affiliated Hospital of Nanchang University, No.1 Mingde Road, Donghu District, Nanchang, 330006, Jiangxi Province, China. 1554597615@qq.com.
Nanchang University · CNSecond Affiliated Hospital of Nanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBrain metastasis (BM) is a dreadful complication that significantly impacts the quality of life in breast cancer patients. A key process during brain metastasis is the migration of cancer cells across blood-brain barrier (BBB). However, the role of snoRNAs regulating BBB in BM is still unknown.

methodsHere SNORic and GEO databases were used to identify differentially expressed snoRNAs between brain metastatic and non-metastatic breast cancer (BC) tissues. The effects of SNORA71B on the capacities of proliferation, migration, invasion, epithelial-mesenchymal transition (EMT), and BBB invasion of BC cells were evaluated by CCK8, transwell, western blot, and BBB model, respectively.

resultsSNORA71B was highly expressed in high BM BC tissues and cells compared to low BM BC controls. Survival analysis revealed high expression of SNORA71B was significantly associated with poor PPS and OS in breast cancer patients. ROC curve showed that SNORA71B might act as biomarker for breast cancer. Moreover, SNORA71B significantly promoted proliferation, migration, and invasion of BC cells with different BM abilities. Importantly, SNORA71B promoted the EMT process of low BM BC cells. SNORA71B knockdown inhibited the high BM BC cells across BBB, while EMT activator dramatically abrogated this inhibited effect.

conclusionsIn conclusion, SNORA71B promotes BC cells across the BBB partly via inducing EMT.

Indexed as

Gene Expression Regulation, NeoplasticBlood-Brain BarrierBrain NeoplasmsBreast NeoplasmsCell Line, TumorCell MovementCell ProliferationDatasets as TopicDisease ProgressionEpithelial-Mesenchymal TransitionFemaleGene Expression ProfilingGene Knockdown TechniquesHumansKaplan-Meier EstimateOligonucleotide Array Sequence AnalysisRNA, Small NucleolarBlood–brain barrierBrain metastasesBreast cancerEpithelial-mesenchymal transitionSNORA71B

Identifiers

PMID32458152
PMCPMC7567732
OpenAlexW3029986330

What OpenQuestion holds

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LicenceCC BY
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.