Evidence map›Paper›PMID 31528235›Full record

ArticleJournal of Cancer2019

MiR-486-5p inhibits IL-22-induced epithelial-mesenchymal transition of breast cancer cell by repressing Dock1.

Hongli Li, Qingjie Mou, Peirui Li, Zhiyi Yang, Zhaoyan Wang, Jie Niu, Yuanyuan Liu, Zhiliang Sun, Shijun Lv, Baogang Zhang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
  2. Subtype-Specific mInternational journal of molecular sciences · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. The role of IL-22 in cancer.Medical oncology (Northwood, London, England) · 2024
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. MicroRNAs: A Link between Mammary Gland Development and Breast Cancer.International journal of molecular sciences · 2022
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 1 institution in 1 country.

Hongli LiMedicine Research Center, Weifang Medical University, Weifang, China.
Qingjie MouDepartment of Oncology, Clinical Medical College, Weifang Medical University, Weifang, China.
Peirui LiDepartment of Thyroid and Breast Surgery, Affiliated Hospital of Weifang Medical University, Weifang, China.
Zhiyi YangDepartment of Pathology, Clinical Medical College, Weifang Medical University, Weifang, China.
Zhaoyan WangDepartment of Pathology, Clinical Medical College, Weifang Medical University, Weifang, China.
Jie NiuCollege of Nursing, Weifang Medical University, Weifang, China.
Yuanyuan LiuCollege of Nursing, Weifang Medical University, Weifang, China.
Zhiliang SunCollege of Biological Science and Technology, Weifang Medical University, Weifang, China.
Shijun LvDepartment of Pathology, Clinical Medical College, Weifang Medical University, Weifang, China.
Baogang ZhangDepartment of Pathology, Clinical Medical College, Weifang Medical University, Weifang, China.
Chonggao YinCollege of Nursing, Weifang Medical University, Weifang, China.
Weifang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epithelial-mesenchymal transition (EMT) is one of important steps that lead to cancer metastasis. Interleukin-22 (IL-22) is a T helper 17 (Th17) cells-secreted cytokine, it can promote invasion and metastasis of many cancers. MiR-486-5p is a microRNA that known to function as a tumor suppressor, and bioinformatics analysis predicts that Dock-1 has a binding site of miR-486-5p. In current research, we examined the relative expression levels of miR-486-5p and Dock-1 in 80 pairs of breast cancer tissues and corresponding adjacent normal tissues, also the effects of modifying their levels in cultured cells. We illustrated that IL-22 and Dock1 promote the invasion, metastasis, and EMT of breast cancer using Transwell invasion assay, western blot and immunofluorescence. MiR-486-5p directly bound the Dock1 mRNA 3' untranslated region and inhibited IL-22-induced EMT of breast cancer cells via the Dock1/NF-κB/Snail signaling pathway. Dock1 overexpression reversed the effect caused by the overexpression of miR-486-5p. Overexpression of miR-486-5p or downregulation of Dock1 reduced pulmonary metastasis in mice. This study provided insight into a potential mechanism where miRNAs regulate breast cancer metastasis and provided a novel therapeutic target for breast cancer treatment.

Indexed as

breast cancerDock1epithelial-mesenchymal transitionIL-22miR-486-5p

Identifiers

PMID31528235
PMCPMC6746125
OpenAlexW2973051899

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.