Evidence map›Paper›PMID 19074980›Full record

ArticleNeuro-oncology2008

Regulatory effect of nerve growth factor in alpha9beta1 integrin-dependent progression of glioblastoma.

Meghan C Brown, Izabela Staniszewska, Philip Lazarovici, George P Tuszynski, Luis Del Valle, Cezary Marcinkiewicz

Open access · bronzeAbstract read
In one paragraph

Article in Neuro-oncology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 13% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Nerve growth factor receptor (NGFR): A key player in glioblastoma progression.Biochimica et biophysica acta. Reviews on cancer · 2026
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Snake venom bioprospecting as an approach to finding potential anti-glioblastoma molecules.The journal of venomous animals and toxins including tropical diseases · 2024
    Review
  8. Review
  9. Article
  10. Article
  11. ProNGF Expression and Targeting in Glioblastoma Multiforme.International journal of molecular sciences · 2023
    Article
  12. Article
  13. Article
  14. Anti-tumor effects of vitamin D in glioblastoma: mechanism and therapeutic implications.Laboratory investigation; a journal of technical methods and pathology · 2022
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  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

6 authors at 1 institution in 2 countries.

Meghan C BrownDepartment of Neuroscience, Center for Neurovirology and Cancer Biology, School of Medicine, Temple University, Philadelphia, PA, USA.
Izabela Staniszewska
Philip Lazarovici
George P Tuszynski
Luis Del Valle
Cezary Marcinkiewicz
Hebrew University of Jerusalem · IL

Funding

VIRAL MODEL FOR TUMOR PATHOGENESIS IN BRAINP01NS036466 · NINDS · TEMPLE UNIV OF THE COMMONWEALTH · PI KHALILI, KAMEL · 1996 to 2007
$6.6M
Targeting alfa 1beta1 integrin in cancer developmentR01CA100145 · NCI · TEMPLE UNIV OF THE COMMONWEALTH · PI MARCINKIEWICZ, CEZARY · 2004 to 2007
$934k
NCI NIH HHS CA100145NCI NIH HHS R01 CA100145NINDS NIH HHS P01 NS036466NINDS NIH HHS P01 NS36466
6 · The paper itself

Abstract

In the present study we described the role of alpha9beta1 integrin in glioblastoma progression following its interaction with nerve growth factor (NGF). The level of expression of alpha9beta1 on astrocytomas is correlated with increased grade of this brain tumor and is highest on glioblastoma, whereas normal astrocytes do not express this integrin. Two glioblastoma cell lines, LN229 and LN18, that are alpha9beta1 integrin positive and negative, respectively, were used for alpha9beta1 integrin-dependent NGF-induced tumor progression. NGF was a significant promoter of promigratory and pro-proliferative activities of glioblastoma cells through direct interaction with alpha9beta1 integrin and activation of MAPK Erk1/2 pathway. The level of NGF increases approximately threefold in the most malignant glioma tissue when compared with normal brain. This increase is related to secretion of NGF by tumor cells. Specific inhibitors of alpha9beta1 integrin or gene silencing inhibited NGF-induced proliferation of LN229 cell line to the level shown by LN18 cells. VLO5 promoted alpha9beta1-dependent programmed cell death by induction of intrinsic apoptosis pathway in cancer cells. LN229 cells were rescued from proapoptotic effect of VLO5 by the presence of NGF. This disintegrin significantly inhibited tumor growth induced by implantation of LN229 cells to the chorioallantoic membrane (CAM) of quail embryonic model, and this inhibitory effect was significantly abolished by the presence of NGF. alpha9beta1 integrin appears to be an interesting target for blocking the progression of malignant gliomas, especially in light of the stimulatory effect of NGF on the development of these tumors and its ability to transfer proapoptotic signals in cancer cells.

Indexed as

AnimalsApoptosisBlotting, WesternBrain NeoplasmsCell Line, TumorDisease ProgressionEnzyme-Linked Immunosorbent AssayGlioblastomaHumansImmunohistochemistryIntegrinsNerve Growth FactorXenograft Model Antitumor Assaysintegrin alpha 9 beta 1IntegrinsNerve Growth Factor

Identifiers

PMID19074980
PMCPMC2719011
OpenAlexW1969522550

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.