Evidence map›Paper›PMID 23826488›Full record

ArticleIranian journal of basic medical sciences2013

Identification of novel hypoxia response genes in human glioma cell line a172.

Fatemeh Baghbani, Reza Raoofian, Mohammad Hasanzadeh Nazarabadi, Tayebeh Hamzehloei, Mohammad Soukhtanloo, Mansur Heidari, Seyed Morteza Afsharzadeh, Sahar Shekouhi, Fahimeh Moradi, Abdol-Azim Sarli and 2 more

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Article in Iranian journal of basic medical sciences, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

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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

4 citing papers in PubMed.

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4 · The record

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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

12 authors.

Fatemeh BaghbaniDepartment of Medical Genetics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Reza Raoofian
Mohammad Hasanzadeh Nazarabadi
Tayebeh Hamzehloei
Mohammad Soukhtanloo
Mansur Heidari
Seyed Morteza Afsharzadeh
Sahar Shekouhi
Fahimeh Moradi
Abdol-Azim Sarli
Javad Zavar-Reza
Majid Mojarrad

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

OBJECTIVE(S): Hypoxia is a serious challenge for treatment of solid tumors. This condition has been manifested to exert significant therapeutic effects on glioblastoma multiform or (WHO) astrocytoma grade IV. Hypoxia contributes numerous changes in cellular mechanisms such as angiogenesis, metastasis and apoptosis evasion. Furthermore, in molecular level, hypoxia can cause induction of DNA breaks in tumor cells. Identification of mechanisms responsible for these effects can lead to designing more efficient therapeutic strategies against tumor progression which results in improvement of patient prognosis. Materials and Methods : In order to identify more hypoxia regulated genes which may have a role in glioblastoma progression, cDNA-AFLP was optimized as a Differential display method which is able to identify and isolate transcripts with no prior sequence knowledge.

resultsUsing this method, the current study identified 120 Transcription Derived Fragments (TDFs) which were completely differentially regulated in response to hypoxia. By sequence homology searching, the current study could detect 22 completely differentially regulated known genes and two unknown sequence matching with two chromosome contig and four sequence matches with some Expressed Sequence Tags (ESTs).

conclusionFurther characterizing of these genes may help to achieve better understanding of hypoxia mediated phenotype change in tumor cells.

Indexed as

cDNA-AFLPGlioblastomaHypoxia

Identifiers

PMID23826488
PMCPMC3700041

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