Evidence map›Paper›PMID 22266868›Full record

ArticleOncogene2012

Angiogenin functionally interacts with p53 and regulates p53-mediated apoptosis and cell survival.

S Sadagopan, M V Veettil, S Chakraborty, N Sharma-Walia, N Paudel, V Bottero, B Chandran

Abstract read
In one paragraph

Article in Oncogene, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.5field-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

25 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  8. Review
  9. Article
  10. Article
  11. Three decades of research on angiogenin: a review and perspective.Acta biochimica et biophysica Sinica · 2016
    Review
  12. Article
  13. Mechanism and Function of Angiogenin in Apoptosis Regulation.Zhongguo sheng wu hua xue yu fen zi sheng wu xue bao = Chinese journal of biochemistry and molecular biology · 2015
    Article
  14. Article
  15. Article
  16. Article
  17. G-quadruplex structures contribute to the neuroprotective effects of angiogenin-induced tRNA fragments.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  18. Article
  19. Article
  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

7 authors at 1 institution in 1 country.

S SadagopanDepartment of Microbiology and Immunology, H.M. Bligh Cancer Research Laboratories, Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.
M V Veettil
S Chakraborty
N Sharma-Walia
N Paudel
V Bottero
B Chandran
Rosalind Franklin University of Medicine and Science · US

Funding

ANTIGENS OF KAPOSIS SARCOMA ASSOCIATED HERPESVIRUSR01CA075911 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI CHANDRAN, BALA · 1998 to 2012
$3.5M
HHV-8, angiogenesis and inflammationR56AI091767 · NIAID · ROSALIND FRANKLIN UNIV OF MEDICINE & SCI · PI CHANDRAN, BALA · 2011 to 2011
$386k
NCI NIH HHS R01 CA075911NIAID NIH HHS AI 091767NIAID NIH HHS R56 AI091767
6 · The paper itself

Abstract

Angiogenin, a 14-kDa multifunctional pro-angiogenic growth factor, is upregulated in several types of cancers. Anti-angiogenin monoclonal antibodies used as antagonists inhibited the establishment, progression and metastasis of human cancer cells in athymic mice (Olson et al., 1994). Silencing angiogenin and inhibition of angiogenin's nuclear translocation blocked cell survival and induced cell death in B-lymphoma and endothelial cells latently infected with Kaposi sarcoma-associated herpesvirus (Sadagopan et al., 2009), suggesting that actively proliferating cancer cells could be inducing angiogenin for inhibiting apoptotic pathways. However, the mechanism of cell survival and apoptosis regulation by angiogenin and their functional significance in cancer is not known. We demonstrate that angiogenin interacts with p53 and colocalizes in the nucleus. Silencing endogenous angiogenin induced p53 promoter activation and p53 target gene (p53, p21 and Bax) expression, downregulated anti-apoptotic Bcl-2 gene expression and increased p53-mediated cell death. In contrast, angiogenin expression blocked pro-apoptotic Bax and p21 expression, induced Bcl-2 and blocked cell death. Angiogenin also co-immunoprecipitated with p53 regulator protein Mdm2. Angiogenin expression resulted in the inhibition of p53 phosphorylation, increased p53-Mdm2 interaction, and consequently increased ubiquitination of p53. Taken together, these studies demonstrate that angiogenin promotes the inhibition of p53 function to mediate anti-apoptosis and cell survival. Our results reveal for the first time a novel p53 interacting function of angiogenin in anti-apoptosis and survival of cancer cells and suggest that targeting angiogenin could be an effective therapy for several cancers.

Indexed as

Apoptosisbcl-2-Associated X ProteinCell DeathCell NucleusCell SurvivalCyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsDown-RegulationEndothelial CellsGene ExpressionHCT116 CellsHeLa CellsHep G2 CellsHerpesvirus 8, HumanHumansPhosphorylationangiogeninbcl-2-Associated X ProteinCyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsMDM2 protein, humanProto-Oncogene Proteins c-mdm2Ribonuclease, PancreaticTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID22266868
PMCPMC3337890
OpenAlexW2090063087

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.