Evidence map›Paper›PMID 24489730›Full record

ArticlePloS one2014

Small activating RNA restores the activity of the tumor suppressor HIC-1 on breast cancer.

Feng Zhao, Shengli Pan, Yan Gu, Shanyu Guo, Qiancheng Dai, Yingyan Yu, Wei Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. miR‑28‑5p inhibits the migration of breast cancer by regulating WSB2.International journal of molecular medicine · 2020
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Mutual interaction between BCL6 and miRNAs contributing to the pathogenesis of various cancers.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2015
    Review
  11. 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

7 authors at 2 institutions in 1 country.

Feng ZhaoDepartment of Surgery, The Ninth People's Hospital of Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Shengli PanDepartment of Surgery, Shanghai Ruijin Hospital of Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Yan GuDepartment of Surgery, The Ninth People's Hospital of Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Shanyu GuoDepartment of Surgery, The Ninth People's Hospital of Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Qiancheng DaiDepartment of Surgery, The Ninth People's Hospital of Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Yingyan YuDepartment of Surgery, Shanghai Ruijin Hospital of Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Wei ZhangDepartment of Surgery, The Ninth People's Hospital of Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Shanghai Jiao Tong University · CNShanghai Ninth People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HIC-1 is a gene that is hypermethylated in cancer, and commonly downregulated in human breast cancer. However, the precise mechanisms and molecular pathways regulated by HIC-1 remain unclear. We assessed HIC-1 expression on a tissue microarray containing 80 cases of breast cancer. We also analyzed its biological function by restoring HIC-1 expression using 5-aza-2' deoxycytidine (5-CdR) and small-activating RNAs for the reversal of HIC-1 tumor suppressive effects on MCF-7 and MDA-MB-231 cell lines. An Agilent Q44h global expressing microarray was probed after restoring the expression of HIC-1. Data demonstrated that HIC-1 expression was reduced significantly in breast cancer tissues. HIC-1 immunohistochemistry resulted in mean staining scores in cancer tissue and normal ductal epithelia of 3.54 and 8.2, respectively (p<0.01). 5-CdR partially reversed HIC-1 expression, and modulated cell growth and apoptosis. dsHIC1-2998, an saRNA, showed activating efficacy in breast cancer cells. A group of differentially expressed genes were characterized by cDNA microarray. Upon saRNA treatment, genes upregulated included those involved in immune activation, cell cycle interference, the induction of apoptosis, anti-metastasis, and cell differentiation. Downregulated genes included oncogenes and those that play roles in cell invasion, cell growth, and cell division. Our findings may provide valuable resources not only for gene functional studies, but also for potential clinical applications to develop novel drug targets.

Indexed as

AdultApoptosisAzacitidineBreast NeoplasmsCell Line, TumorCell ProliferationDecitabineDown-RegulationFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansImmunohistochemistryKruppel-Like Transcription FactorsOligonucleotide Array Sequence AnalysisRNAAzacitidineDecitabineHIC1 protein, humanKruppel-Like Transcription FactorsRNA

Identifiers

PMID24489730
PMCPMC3904905
OpenAlexW2025964091

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.