Evidence map›Paper›PMID 29072689›Full record

ArticleCell death & disease2017

MiR-629 promotes human pancreatic cancer progression by targeting FOXO3.

Haijiao Yan, Qing Li, Jun Wu, Wenwei Hu, Jingting Jiang, Liangrong Shi, Xin Yang, Danxia Zhu, Mei Ji, Changping Wu

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Article
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  4. Review
  5. Article
  6. Article
  7. Forkhead box O proteins: steering the course of stem cell fate.Cell regeneration (London, England) · 2024
    Review
  8. Review
  9. Frontiers in oncology · 2024
    Article
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  19. Observational
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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

10 authors at 1 institution in 1 country.

Haijiao YanDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou 213003, P.R. China.
Qing LiDepartment of Pathology, The Third Affiliated Hospital of Soochow University, Changzhou 213003, P.R. China.
Jun WuDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou 213003, P.R. China.
Wenwei HuDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou 213003, P.R. China.
Jingting JiangDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou 213003, P.R. China.
Liangrong ShiDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou 213003, P.R. China.
Xin YangDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou 213003, P.R. China.
Danxia ZhuDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou 213003, P.R. China.
Mei JiDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou 213003, P.R. China.
Changping WuDepartment of Oncology, The Third Affiliated Hospital of Soochow University, Changzhou 213003, P.R. China.
Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The FOXO signaling pathway has been reported to have an important role in human cancer. Expression of miR-629 was markedly upregulated in pancreatic cancer and negatively correlated with FOXO3. Therefore, exploring the regulatory mechanism of miR-629 and FOXO3 signaling may provide valuable clinical targets for pancreatic cancer therapy. In the current study, we found that overexpressing and inhibiting miR-629, respectively, enhanced and reduced the cell proliferation and metastasis of pancreatic cancer cells in vitro and in vivo compared with parental cells or cells transfected with a control vector. Furthermore, we found that miR-629 negatively regulated FOXO3 protein expression and decreased the activity of a luciferase reporter construct containing the FOXO3 3'-untranslated region. These results show that miR-629 regulates FOXO3 at the posttranscriptional level, resulting in enhanced cell proliferation and invasion of pancreatic carcinoma. Furthermore, we found that overexpressing miR-629 enhanced, while inhibiting miR-629 reduced, the stem cell-like phenotype of pancreatic cancer cells in vitro. A functional polymorphism at miR-629-binding site in the 3'-UTR of FOXO3 gene confers a decreased risk of progression in pancreatic carcinoma. Furthermore, these findings suggest that miR-629 has a vital role in promoting the development of pancreatic cancer and may represent a novel prognostic biomarker and therapeutic target.

Indexed as

Cell ProliferationDisease ProgressionForkhead Box Protein O3HumansMicroRNAsPancreatic NeoplasmsForkhead Box Protein O3FOXO3 protein, humanMicroRNAsMIRN629 microRNA, human

Identifiers

PMID29072689
PMCPMC5682687
OpenAlexW2767074454

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.