Evidence map›Paper›PMID 36737605›Full record

ArticleCell death & disease2023

CCN3/NOV promotes metastasis and tumor progression via GPNMB-induced EGFR activation in triple-negative breast cancer.

Seogho Son, Hyungjoo Kim, Hogeun Lim, Joo-Hyung Lee, Kyung-Min Lee, Incheol Shin

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. The advance of CCN3 in fibrosis.Journal of cell communication and signaling · 2023
    Review
  11. Article
  12. CCN proteins: opportunities for clinical studies-a personal perspective.Journal of cell communication and signaling · 2023
    Review
  13. Human Antibody VMolecular pharmaceutics · 2023
    Article
  14. 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

6 authors at 1 institution in 1 country.

Seogho SonDepartment of Life Science, Hanyang University, Seoul, 04763, Korea.
Hyungjoo KimDepartment of Life Science, Hanyang University, Seoul, 04763, Korea.
Hogeun LimDepartment of Life Science, Hanyang University, Seoul, 04763, Korea.
Joo-Hyung LeeDepartment of Life Science, Hanyang University, Seoul, 04763, Korea.
Kyung-Min LeeDepartment of Life Science, Hanyang University, Seoul, 04763, Korea.
Incheol ShinDepartment of Life Science, Hanyang University, Seoul, 04763, Korea. incheol@hanyang.ac.kr.ORCID 0000-0003-3172-2594
Hanyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is the most aggressive subtype of breast cancer. TNBC patients typically exhibit unfavorable outcomes due to its rapid growth and metastatic potential. Here, we found overexpression of CCN3 in TNBC patients. We identified that CCN3 knockdown diminished cancer stem cell formation, metastasis, and tumor growth in vitro and in vivo. Mechanistically, ablation of CCN3 reduced activity of the EGFR/MAPK pathway. Transcriptome profiling revealed that CCN3 induces glycoprotein nonmetastatic melanoma protein B (GPNMB) expression, which in turn activates the EGFR pathway. An interrogation of the TCGA dataset further supported the transcriptional regulation of GPNMB by CCN3. Finally, we showed that CCN3 activates Wnt signaling through a ligand-dependent or -independent mechanism, which increases microphthalmia-associated transcription factor (MITF) protein, a transcription factor inducing GPNMB expression. Together, our findings demonstrate the oncogenic role of CCN3 in TNBC, and we propose CCN3 as a putative therapeutic target for TNBC.

Indexed as

Triple Negative Breast NeoplasmsCell Line, TumorCell ProliferationErbB ReceptorsHumansMembrane GlycoproteinsNephroblastoma Overexpressed ProteinTranscription FactorsCCN3 protein, humanEGFR protein, humanErbB ReceptorsGPNMB protein, humanMembrane GlycoproteinsNephroblastoma Overexpressed ProteinTranscription Factors

Identifiers

PMID36737605
PMCPMC9898537
OpenAlexW4319079771

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.