Evidence map›Paper›PMID 24733393›Full record

ArticleThe Journal of biological chemistry2014

The tetraspanin CD81 protein increases melanoma cell motility by up-regulating metalloproteinase MT1-MMP expression through the pro-oncogenic Akt-dependent Sp1 activation signaling pathways.

In-Kee Hong, Hee-Jung Byun, Jaeseob Lee, Young-June Jin, Sun-Ju Wang, Doo-Il Jeoung, Young-Myeong Kim, Hansoo Lee

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing 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

51 citing papers in PubMed, 79 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. The molecular mechanism of CD81 antibody inhibition of metastasis.Proceedings of the National Academy of Sciences of the United States of America · 2023
    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

8 authors at 3 institutions in 2 countries.

In-Kee HongFrom the Medical and Bio-Material Research Center and.
Hee-Jung ByunFrom the Medical and Bio-Material Research Center and.
Jaeseob LeeBrain Korea 21+ Graduate Program, Department of Biological Sciences, College of Natural Sciences, and.
Young-June JinFrom the Medical and Bio-Material Research Center and.
Sun-Ju WangDepartment of Biological Sciences, College of Natural Sciences, and.
Doo-Il JeoungFrom the Medical and Bio-Material Research Center and.
Young-Myeong KimDepartment of Molecular and Cellular Biochemistry, School of Medicine, Kangwon National University, Chunchon, Kangwon-do 200-701, Republic of Korea.
Hansoo LeeFrom the Medical and Bio-Material Research Center and Brain Korea 21+ Graduate Program, Department of Biological Sciences, College of Natural Sciences, and hslee@kangwon.ac.kr.
Material (Belgium) · BEKorea Institute of Brain Science · KRKangwon National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the importance of multiple tetraspanin proteins in cancer invasion and metastasis, little is known about the role and significance of tetraspanin CD81 in these processes. In the present study, we examined CD81 effects on melanoma cell invasiveness and metastasis. Transfection of CD81 into melanoma cells lacking endogenous CD81 expression significantly enhanced the migrating, invasive, and metastatic abilities of melanoma cells. Interestingly, membrane type 1 matrix metalloproteinase (MT1-MMP) expression was found in CD81-expressing melanoma cells but not in CD81-deficient cells. siRNA knockdown of CD81 in melanoma cells with endogenous CD81 demonstrated decreased MT1-MMP levels and cell motility. Notably, CD81-induced cell migration was abrogated by antibody blocking and siRNA knockdown of MT1-MMP, indicating that MT1-MMP is responsible for CD81-stimulated melanoma cell migration. Promoter analysis revealed an essential role of the Sp1 transcription factor in CD81-induced MT1-MMP transcription. We also demonstrate that the Sp1-activating Akt pathway is involved in adhesion-dependent CD81 signaling to induce MT1-MMP expression and cell motility. Importantly, human skin cancer tissue specimens displayed a positive correlation of CD81 with MT1-MMP expression levels and a close association of CD81 with malignant melanomas. Taken together, these results strongly suggest that CD81 stimulates melanoma cell motility by inducing MT1-MMP expression through the Akt-dependent Sp1 activation signaling pathway, leading to increased melanoma invasion and metastasis.

Indexed as

Basal Cell CarcinomaCarcinoma, Squamous CellCell Line, TumorCell MovementGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticHumansMatrix Metalloproteinase 14MelanomaNeoplasm InvasivenessProto-Oncogene Proteins c-aktRNA, Small InterferingSignal TransductionSkin NeoplasmsSp1 Transcription FactorTetraspanin 28AKT1 protein, humanCD81 protein, humanMatrix Metalloproteinase 14MMP14 protein, humanProto-Oncogene Proteins c-aktRNA, Small InterferingSp1 Transcription FactorTetraspanin 28Cell MotilityCell SignalingInvasionMelanomaSp1Tetraspanins

Identifiers

PMID24733393
PMCPMC4140923
OpenAlexW1989883027

What OpenQuestion holds

Textmetadata
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.