Evidence map›Paper›PMID 25425968›Full record

ArticleNeoplasia (New York, N.Y.)2014

Galectin-3 inhibits osteoblast differentiation through notch signaling.

Kosei Nakajima, Dhong Hyo Kho, Takashi Yanagawa, Yosuke Harazono, Xiaoge Gao, Victor Hogan, Avraham Raz

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
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

54 citing papers in PubMed, 82 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Inflammaging-Driven Osteoporosis: Is a Galectin-Targeted Approach Needed?International journal of molecular sciences · 2025
    Review
  7. Article
  8. Role of Galectin-1 in the Pathogenesis of Melanoma.Journal of cancer science and clinical therapeutics · 2025
    Article
  9. Article
  10. The Bioactive Compounds ofPharmaceuticals (Basel, Switzerland) · 2024
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. SREBP1 regulatesMolecular therapy. Nucleic acids · 2022
    Article
  18. Review
  19. Article
  20. 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

7 authors at 3 institutions in 2 countries.

Kosei NakajimaDepartments of Oncology and Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, USA.
Dhong Hyo KhoDepartments of Oncology and Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, USA.
Takashi YanagawaDepartment of Orthopedic Surgery, Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan.
Yosuke HarazonoDepartments of Oncology and Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, USA.
Xiaoge GaoDepartments of Oncology and Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, USA.
Victor HoganDepartments of Oncology and Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, USA.
Avraham RazDepartments of Oncology and Pathology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI, USA.
Wayne State University · USGunma University · JPThe Barbara Ann Karmanos Cancer Institute · US

Funding

The Role of Tumor Cell Surface Lectin in MetastasesR37CA046120 · NCI · WAYNE STATE UNIVERSITY · PI RAZ, AVRAHAM · 2007 to 2014
$3.0M
NCI NIH HHS R37 CA046120NCI NIH HHS R37 CA46120
6 · The paper itself

Abstract

Patients with bone cancer metastasis suffer from unbearable pain and bone fractures due to bone remodeling. This is caused by tumor cells that disturb the bone microenvironment. Here, we have investigated the role of tumor-secreted sugar-binding protein, i.e., galectin-3, on osteoblast differentiation and report that it downregulates the expression of osteoblast differentiation markers, e.g., RUNX2, SP7, ALPL, COL1A1, IBSP, and BGLAP, of treated human fetal osteoblast (hFOB) cells. Co-culturing of hFOB cells with human breast cancer BT-549 and prostate cancer LNCaP cells harboring galectin-3 has resulted in inhibition of osteoblast differentiation by the secreted galectin-3 into culture medium. The inhibitory effect of galectin-3 was found to be through its binding to Notch1 in a sugar-dependent manner that has led to accelerated Notch1 cleavage and activation of Notch signaling. Taken together, our findings show that soluble galectin-3 in the bone microenvironment niche regulates bone remodeling through Notch signaling, suggesting a novel bone metastasis therapeutic target.

Indexed as

Cell DifferentiationSignal TransductionAlkaline PhosphataseCalciumCell LineCell Line, TumorCoculture TechniquesCollagen Type ICollagen Type I, alpha 1 ChainCore Binding Factor Alpha 1 SubunitGalectin 3Gene ExpressionHEK293 CellsHumansIntegrin-Binding SialoproteinMicroscopy, ConfocalAlkaline PhosphataseCalciumCollagen Type ICollagen Type I, alpha 1 ChainCore Binding Factor Alpha 1 SubunitGalectin 3IBSP protein, humanIntegrin-Binding SialoproteinNOTCH1 protein, humanReceptor, Notch1RUNX2 protein, human

Identifiers

PMID25425968
PMCPMC4240919
OpenAlexW2029642204

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.