Evidence map›Paper›PMID 24785261›Full record

ArticleEpigenetics2014

Epigenetically regulated MIR941 and MIR1247 target gastric cancer cell growth and migration.

Joong-Gook Kim, Tae-Oh Kim, Jin-Han Bae, Jae-Woong Shim, Myoung Joo Kang, Kwangmo Yang, Angela H Ting, Joo Mi Yi

Open access · bronzeAbstract read
In one paragraph

Article in Epigenetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.0field-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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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  11. Epigenetics and MicroRNAs in Cancer.International journal of molecular sciences · 2018
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Dysregulation of non-coding RNAs in gastric cancer.World journal of gastroenterology · 2015
    Review
  18. Article
  19. 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

8 authors at 3 institutions in 2 countries.

Joong-Gook KimResearch Center; Dongnam Institute of Radiological & Medical Sciences (DIRAMS); Busan, South Korea.
Tae-Oh KimDepartment of Internal Medicine; Inje University Haeundae Paik Hospital; Busan, South Korea.
Jin-Han BaeResearch Center; Dongnam Institute of Radiological & Medical Sciences (DIRAMS); Busan, South Korea.
Jae-Woong ShimResearch Center; Dongnam Institute of Radiological & Medical Sciences (DIRAMS); Busan, South Korea.
Myoung Joo KangDepartment of Internal Medicine; Inje University Haeundae Paik Hospital; Busan, South Korea.
Kwangmo YangResearch Center; Dongnam Institute of Radiological & Medical Sciences (DIRAMS); Busan, South Korea.
Angela H TingGenomic Medicine Institute; Lerner Research Institute; Cleveland Clinic Foundation; Cleveland, OH USA.
Joo Mi YiResearch Center; Dongnam Institute of Radiological & Medical Sciences (DIRAMS); Busan, South Korea.
Dongnam Institute of Radiological & Medical Sciences · KRInje University Haeundae Paik Hospital · KRCerner (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Altered expression of microRNA (miRNA) can significantly contribute to cancer development and recent studies have shown that a number of miRNAs may be regulated by DNA methylation. Through a candidate gene approach, we identified MIR941 and MIR1247 to be transcriptionally silenced by DNA hypermethylation in several gastric cancer cell lines. We confirmed that these miRNAs are also densely methylated in primary gastric cancers but not in normal gastric tissues. In addition, we demonstrated that ectopic expression of these two miRNAs in AGS gastric cancer cells resulted in suppression of growth and migration. Furthermore, we tested genes predicted to be the targets of MIR941 and MIR1247 and identified 7 and 6 genes, whose expressions were significantly downregulated by transfection of MIR941 and MIR1247 mimics, respectively, in gastric cancer cell lines. Some of these genes are known to promote proliferation and invasion, phenotypes we observed upon ectopic expression of the two miRNAs. Thus, we examined these candidates more closely and found that downregulation of mRNA corresponded to a decrease in protein levels (observed by western blot). Our study provides unequivocal evidence that MIR941 and MIR1247 are transcriptionally regulated by DNA methylation in gastric cancer and that they have tumor suppressor properties through their inhibition of key cancer promoting genes in this context.

Indexed as

Cell MovementCell ProliferationEpigenesis, GeneticAdenocarcinomaAdenomaAdultAgedAged, 80 and overCell Line, TumorDNA MethylationFemaleGene SilencingHumansMaleMicroRNAsMiddle AgedMicroRNAsRNA, Messenger5-aza-2'-deoxycytidineDNA methylationepigeneticsgastric cancermicroRNAMIR1247MIR941

Identifiers

PMID24785261
PMCPMC4143404
OpenAlexW2005687485

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.