Evidence map›Paper›PMID 19724901›Full record

ArticleInternational journal of oncology2009

Generation of an immortalized astrocyte cell line from H-2Kb-tsA58 mice to study the role of astrocytes in brain metastasis.

Robert R Langley, Dominic Fan, Lixia Guo, Chenyu Zhang, Qingtang Lin, Emily C Brantley, Joseph H McCarty, Isaiah J Fidler

Open access · bronzeAbstract read
In one paragraph

Article in International journal of oncology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.3field-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

31 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
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  5. Review
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  7. Review
  8. Reactive Astrocytes in Brain Metastasis.Frontiers in oncology · 2017
    Review
  9. Article
  10. Article
  11. Macitentan, a Dual Endothelin Receptor Antagonist, in Combination with Temozolomide Leads to Glioblastoma Regression and Long-term Survival in Mice.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Article
  12. Article
  13. Review
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  15. Article
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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 1 institution in 1 country.

Robert R LangleyDepartment of Cancer Biology, Unit 173, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. rlangley@mdanderson.org
Dominic Fan
Lixia Guo
Chenyu Zhang
Qingtang Lin
Emily C Brantley
Joseph H McCarty
Isaiah J Fidler
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Analysis of alphaVbeta8 Integrin In GliomagenesisR01NS059876 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MCCARTY, JOSEPH H · 2008 to 2012
$1.9M
NCI NIH HHS CA16672NCI NIH HHS CA902701NCI NIH HHS P30 CA016672NINDS NIH HHS R01 NS059876
6 · The paper itself

Abstract

Astrocytes play a critical role in maintaining cerebral homeostasis and their dysregulation is thought to contribute to the pathogenesis of several diseases, including brain cancer and metastasis. Similar to the human disease, we found that lung and melanoma metastases in the mouse brain are accompanied by a reactive gliosis. To begin to study the biology of astrocytes and examine how these cells might contribute to metastasis formation and progression in the brain, we generated a conditionally immortal astrocyte cell line from H-2Kb-tsA58 mice. Astrocytes grown in culture expressed glial fibrillary acid protein (GFAP), glutamate receptor 1, and the N-methyl-D-aspartate (NMDA) receptor. Astrocytes also expressed the glial-specific transporters excitatory amino acid transporter 1 (EAAT1) and EAAT2. Astrocytes grown under permissive conditions (33 degrees C) expressed SV40 large T antigen and had a doubling time of 36 h, whereas expression of SV40 large T antigen was negligible in astrocytes grown at 37 degrees C for 72 h, which coincided with a plateau in cell division. In a co-culture assay with human lung adenocarcinoma cells (PC14-PE6), astrocytes activated programs in the tumor cells that signal for cell division and survival. Hence, the immortalized cell line will be useful for studying the role of astrocytes in disease processes in the brain, such as metastasis.

Indexed as

AdenocarcinomaAnimalsAnimals, NewbornAntigens, CDAntigens, Differentiation, MyelomonocyticAntigens, Polyomavirus TransformingAstrocytesBrain NeoplasmsCD68 MoleculeCell CommunicationCell LineCell ProliferationCell SurvivalCell Transformation, ViralCoculture TechniquesExcitatory Amino Acid Transporter 1Antigens, CDAntigens, Differentiation, MyelomonocyticAntigens, Polyomavirus TransformingCD68 antigen, humanCD68 MoleculeCD68 protein, mouseExcitatory Amino Acid Transporter 1Excitatory Amino Acid Transporter 2Glial Fibrillary Acidic ProteinH-2 AntigensH-2Kb protein, mouseReceptors, N-Methyl-D-AspartateSlc1a2 protein, mouseSlc1a3 protein, mouse

Identifiers

PMID19724901
PMCPMC2882684
OpenAlexW2051467830

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.