Evidence map›Paper›PMID 32325994›Full record

ArticleInternational journal of molecular sciences2020

Chemerin Treatment Inhibits the Growth and Bone Invasion of Breast Cancer Cells.

Hyungkeun Kim, Joo-Hee Lee, Sun Kyoung Lee, Na-Young Song, Seung Hwa Son, Ki Rim Kim, Won-Yoon Chung

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.8field-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

27 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Chemerin/ChemerinR1 axis and inflammation-related diseases.Frontiers in molecular biosciences · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Exploring the multifaceted role of obesity in breast cancer progression.Frontiers in cell and developmental biology · 2024
    Review
  10. Article
  11. Review
  12. The Role of Adipokines in the Pathologies of the Central Nervous System.International journal of molecular sciences · 2023
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  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

7 authors at 3 institutions in 1 country.

Hyungkeun KimDepartment of Applied Life Science, The Graduate School, Yonsei University, Seoul 03722, Korea.
Joo-Hee LeeDepartment of Oral Biology and BK21 PLUS project, Yonsei University College of Dentistry, Seoul 03722, Korea.
Sun Kyoung LeeDepartment of Applied Life Science, The Graduate School, Yonsei University, Seoul 03722, Korea.
Na-Young SongDepartment of Applied Life Science, The Graduate School, Yonsei University, Seoul 03722, Korea.
Seung Hwa SonDepartment of Oral Biology and BK21 PLUS project, Yonsei University College of Dentistry, Seoul 03722, Korea.
Ki Rim KimDepartment of Dental Hygiene, College of Science and Engineering, Kyungpook National University, Sangju 37224, Korea.
Won-Yoon ChungDepartment of Applied Life Science, The Graduate School, Yonsei University, Seoul 03722, Korea.
Yonsei University · KRYonsei University College of DentistryKyungpook National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemerin is secreted as prochemerin from various cell types and then cleaved into the bioactive isoform by specific proteases. In various cancer types, chemerin exhibits pro- or antitumor effects. In the present study, chemerin treatment significantly inhibited the viability and invasion of breast cancer cells in the absence or presence of transforming growth factor (TGF)-β and insulin-like growth factor (IGF)-1. The expression levels of E-cadherin and vimentin were reduced in chemerin-treated breast cancer cells. However, chemerin treatment recovered the reduced E-cadherin expression level in breast cancer cells treated with TGF-β or IGF-1. Chemerin treatment inhibited nuclear β-catenin levels in breast cancer cells stimulated with or without TGF-β or IGF-1. In addition, chemerin treatment blocked the increase in the receptor activator of nuclear factor kappa-Β ligand (RANKL)/osteoprotegerin (OPG) ratio in osteoblastic cells exposed to metastatic breast cancer cell-derived conditioned medium. Chemerin treatment inhibited RANKL-induced osteoclast formation and bone resorption by reducing the secretion of matrix metalloproteinase (MMP)-2, MMP-9, and cathepsin K. Intraperitoneal administration of chemerin inhibited tumor growth in MCF-7 breast cancer cell-injected mice and reduced the development of osteolytic lesions resulting from intratibial inoculation of MDA-MB-231 cells. Taken together, chemerin inhibits the growth and invasion of breast cancer cells and prevents bone loss resulting from breast cancer cells by inhibiting finally osteoclast formation and activity.

Indexed as

AnimalsAntineoplastic AgentsBiomarkersBone NeoplasmsBreast NeoplasmsCell Line, TumorCell MovementCell ProliferationChemokinesDisease Models, AnimalFemaleGene ExpressionHumansImmunophenotypingMiceOsteoprotegerinAntineoplastic AgentsBiomarkersChemokinesOsteoprotegerinRANK LigandRARRES2 protein, humanbone resorptionbreast cancer cell invasionchemerinEMTRANKL/OPG

Identifiers

PMID32325994
PMCPMC7216174
OpenAlexW3017301236

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.