Evidence map›Paper›PMID 14997208›Full record

ArticleBritish journal of cancer2004

Renin and angiotensinogen expression and functions in growth and apoptosis of human glioblastoma.

L Juillerat-Jeanneret, J Celerier, C Chapuis Bernasconi, G Nguyen, W Wostl, H P Maerki, R-C Janzer, P Corvol, J-M Gasc

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

54 citing papers in PubMed, 145 citations in OpenAlex.

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  11. European journal of breast health · 2021
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  13. Angiotensin-converting enzyme 2 gene expression in human male urological tissues: implications for pathogenesis and virus transmission pathways.African journal of urology : the official journal of the Pan African Urological Surgeons' Association (PAUSA) · 2021
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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

9 authors at 3 institutions in 2 countries.

L Juillerat-JeanneretUniversity Institute of Pathology, CHUV, Bugnon 25, Lausanne CH1011, Switzerland. lucienne.juillerat@chuv.hospvd.ch
J Celerier
C Chapuis Bernasconi
G Nguyen
W Wostl
H P Maerki
R-C Janzer
P Corvol
J-M Gasc
Inserm · FRRoche (Switzerland) · CHUniversity Hospital of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The expression and function in growth and apoptosis of the renin-angiotensin system (RAS) was evaluated in human glioblastoma. Renin and angiotensinogen (AGT) mRNAs and proteins were found by in situ hybridisation and immunohistochemistry in glioblastoma cells. Angiotensinogen was present in glioblastoma cystic fluids. Thus, human glioblastoma cells produce renin and AGT and secrete AGT. Human glioblastoma and glioblastoma cells expressed renin, AGT, renin receptor, AT(2) and/or AT(1) mRNAs and proteins determined by RT-PCR and/or Western blotting, respectively. The function of the RAS in glioblastoma was studied using human glioblastoma cells in culture. Angiotensinogen, des(Ang I)AGT, tetradecapaptide renin substrate (AGT1-14), Ang I, Ang II or Ang III, added to glioblastoma cells in culture, did not modulate their proliferation, survival or death. Angiotensin-converting enzyme inhibitors did not diminish glioblastoma cell proliferation. However, the addition of selective synthetic renin inhibitors to glioblastoma cells decreased DNA synthesis and viable tumour cell number, and induced apoptosis. This effect was not counterbalanced by concomitant addition of Ang II. In conclusion, the complete RAS is expressed by human glioblastomas and glioblastoma cells in culture. Inhibition of renin in glioblastoma cells may be a potential approach to control glioblastoma cell proliferation and survival, and glioblastoma progression in combination therapy.

Indexed as

ApoptosisAngiotensin-Converting Enzyme InhibitorsAngiotensinogenAnimalsBrain NeoplasmsCell DivisionCHO CellsCricetinaeGlioblastomaHumansImmunoenzyme TechniquesIn Situ HybridizationProtease InhibitorsReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 2ReninAngiotensin-Converting Enzyme InhibitorsAngiotensinogenProtease InhibitorsReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 2ReninRNA, MessengerSerine Proteinase Inhibitors

Identifiers

PMID14997208
PMCPMC2409624
OpenAlexW1974742704

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.