Evidence map›Paper›PMID 28291253›Full record

ArticleScientific reports2017

Mecp2-mediated Epigenetic Silencing of miR-137 Contributes to Colorectal Adenoma-Carcinoma Sequence and Tumor Progression via Relieving the Suppression of c-Met.

Tao Chen, Shi-Lun Cai, Jian Li, Zhi-Peng Qi, Xu-Quan Li, Le-Chi Ye, Xiao-Feng Xie, Ying-Yong Hou, Li-Qing Yao, Mei-Dong Xu and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Novel Diagnostic Biomarkers in Colorectal Cancer.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Review
  12. Article
  13. MicroRNAs and Long Non-coding RNAs in c-Met-Regulated Cancers.Frontiers in cell and developmental biology · 2020
    Review
  14. Article
  15. Article
  16. HGF/c-MET: A Promising Therapeutic Target in the Digestive System Cancers.International journal of molecular sciences · 2018
    Review
  17. Hypoxia and Selective Autophagy in Cancer Development and Therapy.Frontiers in cell and developmental biology · 2018
    Review
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

13 authors at 3 institutions in 1 country.

Tao ChenEndoscopy center, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Shi-Lun CaiEndoscopy center, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Jian LiEndoscopy center, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Zhi-Peng QiEndoscopy center, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Xu-Quan LiEndoscopy center, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Le-Chi YeDepartment of Oncological Surgery, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.
Xiao-Feng XieDepartment of Pathology, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Ying-Yong HouDepartment of Pathology, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Li-Qing YaoEndoscopy center, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Mei-Dong XuEndoscopy center, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Ping-Hong ZhouEndoscopy center, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Jian-Min XuDepartment of General Surgery, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Yun-Shi ZhongEndoscopy center, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Fudan University · CNSun Yat-sen University · CNWenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The molecular mechanisms underlying colorectal cancer (CRC) development remain elusive. In this study, we examined the miRNA and mRNA expressions in the adenoma-carcinoma sequence (ACS), a critical neoplastic progression in CRC development. We found that miR-137 was down-regulated in all adenoma and carcinoma tissues. Low miR-137 levels were correlated negatively with tumor progression and metastasis. Then we identified the inhibition effect of the miR-137 in CRC development, both in CRC cell lines and mouse models. MiR-137 was shown to control CRC cell proliferation, colony formation, migration and invasion and to control tumor growth and metastasis. We further confirmed the negative association between miR-137 and c-Met expression and thus validated this important oncogene as the target of miR-137 in CRC. In addition, we found a DNA methyl-CpG-binding protein, Mecp2, was up-regulated in ACS tissues via mRNA sequencing. Further experiment showed that miR-137 expression in CRC was subjected to epigenetic regulation mediated by Mecp2. We also confirmed c-Met expression can be up-regulated by silencing of miR-137 and suppressed by coexpression of Mecp2 and miR-137. These findings highlight the critical role of miR-137-c-Met nexus in CRC development and reveal Mecp2-regulated epigenetic silence causes the downregulation of miR-137 in colorectal adenoma and carcinoma.

Indexed as

AdenomaAnimalsCarcinomaCell MovementCell ProliferationColorectal NeoplasmsEpigenesis, GeneticGene Expression Regulation, NeoplasticHCT116 CellsHumansMethyl-CpG-Binding Protein 2MiceMicroRNAsNeoplasm InvasivenessNeoplasm MetastasisProto-Oncogene Proteins c-metMECP2 protein, humanMethyl-CpG-Binding Protein 2MicroRNAsMIRN137 microRNA, humanProto-Oncogene Proteins c-met

Identifiers

PMID28291253
PMCPMC5349564
OpenAlexW2768740980

What OpenQuestion holds

Textmetadata
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.