Evidence map›Paper›PMID 28548936›Full record

ArticleOncotarget2017

MiR-650 represses high-risk non-metastatic colorectal cancer progression via inhibition of AKT2/GSK3β/E-cadherin pathway.

Chunxian Zhou, Fengyun Cui, Jiali Li, Diyi Wang, Yingze Wei, Ying Wu, Jiping Wang, Hongguang Zhu, Shuyang Wang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 27% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Journal of the American Heart Association · 2023
    Article
  5. Review
  6. Article
  7. Review
  8. miR-224 targets3 Biotech · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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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

9 authors at 3 institutions in 2 countries.

Chunxian ZhouDepartment of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Fengyun CuiDepartment of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Jiali LiDepartment of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Diyi WangDepartment of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Yingze WeiDepartment of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Ying WuDepartment of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Jiping WangDivision of Surgical Oncology, Brigham and Women Medicine, Harvard Medical School, Boston, Massachusetts, USA.
Hongguang ZhuDepartment of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Shuyang WangDepartment of Pathology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Shanghai Medical College of Fudan University · CNBrigham and Women's Hospital · USShanghai University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although 5-year survival rate of non-metastatic colorectal cancer (CRC) is high, about 10% of patients in stage I and II still develop into metastatic CRC and eventually die after resection. Currently, there is no effective biomarker for predicting the prognosis of non-metastatic CRC in clinical practice. In this study, we identified miR-650 as a biomarker for prognosis prediction. We observed that the expression of miR-650 in tumor tissues had a positive association with overall survival. MiR-650 inhibited cell growth and invasion in vitro and in vivo. Furthermore, miR-650 targeted AKT2 and repressed the activation of the AKT pathway (AKT2/GSK3β/E-cadherin). Thus it induced the translocation of E-cadherin and β-catenin in cancer cells. Our results highlight the potential of miR-650 as a prognostic prediction biomarker and therapeutic target in non-metastatic CRC via inhibition of the AKT2/GSK3β/E-cadherin pathway.

Indexed as

Gene Expression Regulation, NeoplasticSignal TransductionAgedAged, 80 and overCadherinsCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsDisease ProgressionFemaleGlycogen Synthase Kinase 3 betaHumansMaleMicroRNAsMiddle AgedAKT2 protein, humanCadherinsGlycogen Synthase Kinase 3 betaMicroRNAsMIRN650 microRNA, humanProto-Oncogene Proteins c-aktAKT pathwaymicroRNAnon-metastatic colorectal cancerprognosis biomarker

Identifiers

PMID28548936
PMCPMC5564786
OpenAlexW2614039761

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.