Evidence map›Paper›PMID 19395875›Full record

ArticleCancer biology & therapy2009

ADAM17 promotes breast cancer cell malignant phenotype through EGFR-PI3K-AKT activation.

Xuguang Zheng, Feng Jiang, Mark Katakowski, Zheng Gang Zhang, Qing-e Lu, Michael Chopp

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

50 citing papers in PubMed, 97 citations in OpenAlex.

  1. Polyploidy and Senescence of Cancer Cells: Impact of Cell Fusion.Advances in experimental medicine and biology · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Soluble NKG2D ligands impair CD8Oncology letters · 2023
    Article
  7. Article
  8. ADAM10 and ADAM17-Novel Players in Retinoblastoma Carcinogenesis.International journal of molecular sciences · 2022
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Xuguang ZhengDepartment of Neurology, Henry Ford Hospital, Detroit, MI 48202, USA.
Feng Jiang
Mark Katakowski
Zheng Gang Zhang
Qing-e Lu
Michael Chopp
Henry Ford Health System · USHenry Ford Hospital · USSchlumberger (Ireland) · IE

Funding

VERTERINARY PROJECTP01CA043892 · NCI · UNIVERSITY OF COLORADO DENVER · PI HETZEL, FRED W · 1987 to 2008
$9.9M
Glioma-Treatment with PDT and Anti-Angiogenic AgentsR01CA100486 · NCI · HENRY FORD HEALTH SYSTEM · PI JIANG, FENG · 2004 to 2007
$1.0M
NCI NIH HHS P01 CA043892NCI NIH HHS R01 CA100486
6 · The paper itself

Abstract

A disintegrin and metalloproteinase-17 (ADAM17) is involved in proteolytic ectodomain shedding of several membrane-bound growth factors and cytokines. The expression and activity of ADAM17 increase under some pathological conditions such as stroke and glioma. ADAM17 promotes neural progenitor cell migration and contributes to stroke-induced neurogenesis after stroke and brain tumor growth and invasion. In the present study, we sought to elucidate whether ADAM17 contributes to breast cancer progression and its mechanisms. To this end, we examined the role of ADAM17 in the proliferation, invasion and tube formation of MDA-MB-231 breast cancer cells in vitro. Stable transfection of the MDA-MB-231 cell line with either a plasmid for overexpression of human ADAM17, or a siRNA to ADAM17 was employed in this study to establish high or low ADAM17 expression in breast cancer cells, respectively. For study of mechanism, the ADAM17 inhibitor TAPI-2 and the PI3K-AKT inhibitor LY294002 were used to counteract high ADAM17 expression or the activated PI3K-AKT pathway. Proliferation of MDA-MB-231 breast cancer cells were tested by MTT, Bromodeoxyuridine incorporation assay, growth curve and sulforhodamine B assay. Matrigel invasion assays were used to assess the ability of MDA-MB-231 cells to penetrate the Extra Cellular Matrix. A Matrigel tube formation assay was performed to test capillary tube formation ability. EGFR-PI3K-Akt pathway activation in MDA-MB-231 cells under different ADAM17 expression levels were tested by western blot and ELISA. Our data show that ADAM17 promotes the MDA-MB-231 malignant phenotype by increased proliferation, invasion and angiogenesis. TGFalpha, VEGF secretion and VEGF expression was increasing by ADAM17 and counteracted by ADAM17 siRNA, TAPI-2 and LY294002 in MDA-MB-231 cells. ADAM17 activated, whereas ADAM17 siRNA, TAPI-2 and LY294002 deactivated the EGFR-PI3K-AKT signal pathway, which correlated with MDA-MB-231 cell malignant phenotype changes. This study suggests ADAM17 contributes to breast cancer progression through activation of the EGFR-PI3K-AKT signal pathway.

Indexed as

ADAM17 ProteinADAM ProteinsBreast NeoplasmsCell Line, TumorDisease ProgressionDNA, ComplementaryEndothelial CellsEnzyme ActivationEpidermal Growth FactorErbB ReceptorsFemaleHumansMitogen-Activated Protein Kinase 1Oncogene Protein v-aktPhosphatidylinositol 3-KinasesRNA, Small InterferingADAM17 ProteinADAM17 protein, humanADAM ProteinsDNA, ComplementaryEpidermal Growth FactorErbB ReceptorsMitogen-Activated Protein Kinase 1Oncogene Protein v-aktPhosphatidylinositol 3-KinasesRNA, Small Interfering

Identifiers

PMID19395875
PMCPMC2766867
OpenAlexW2061593125

What OpenQuestion holds

Textmetadata
LicenceTDM
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.