Evidence map›Paper›PMID 22611156›Full record

ArticleBlood2012

Treatment of erythropoietin deficiency in mice with systemically administered siRNA.

William Querbes, Roman L Bogorad, Javid Moslehi, Jamie Wong, Amy Y Chan, Elena Bulgakova, Satya Kuchimanchi, Akin Akinc, Kevin Fitzgerald, Victor Koteliansky and 1 more

Open access · greenAbstract read
In one paragraph

Article in Blood, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.7field-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

22 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. PHD1-3 oxygen sensors in vivo-lessons learned from gene deletions.Pflugers Archiv : European journal of physiology · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Inhibition of fibroblast growth factor 23 (FGF23) signaling rescues renal anemia.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  7. Article
  8. The EGLN-HIF OMolecular cell · 2017
    Review
  9. Anemia of Inflammation: A Review.The Medical clinics of North America · 2017
    Review
  10. The VHL Tumor Suppressor Gene: Insights into Oxygen Sensing and Cancer.Transactions of the American Clinical and Climatological Association · 2017
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Suppression of erythropoiesis by dietary nitrate.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

William QuerbesAlnylam Pharmaceuticals, Cambridge, MA 02215, USA. william_kaelin@dfci.harvard.edu
Roman L Bogorad
Javid Moslehi
Jamie Wong
Amy Y Chan
Elena Bulgakova
Satya Kuchimanchi
Akin Akinc
Kevin Fitzgerald
Victor Koteliansky
William G Kaelin
Alnylam Pharmaceuticals (United States) · USBrigham and Women's Hospital · USHoward Hughes Medical Institute · USMassachusetts Institute of Technology · US

Funding

Treating the P13-Kinase/AKTP50CA101942 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI David McDermott · 2003 to 2026
$53.4M
The von Hippel-Lindau Tumor Suppressor Protein:Roles in Cancer and Oxygen SensingR01CA068490 · NCI · DANA-FARBER CANCER INSTITUTE · PI KAELIN, WILLIAM G. · 1996 to 2015
$4.8M
Howard Hughes Medical InstituteNCI NIH HHS P50 CA101942NCI NIH HHS R01 CA068490
6 · The paper itself

Abstract

Anemia linked to a relative deficiency of renal erythropoietin production is a significant cause of morbidity and medical expenditures in the developed world. Recombinant erythropoietin is expensive and has been linked to excess cardiovascular events. Moreover, some patients become refractory to erythropoietin because of increased production of factors such as hepcidin. During fetal life, the liver, rather than the kidney, is the major source of erythropoietin. In the present study, we show that it is feasible to reactivate hepatic erythropoietin production and suppress hepcidin levels using systemically delivered siRNAs targeting the EglN prolyl hydroxylases specifically in the liver, leading to improved RBC production in models of anemia caused by either renal insufficiency or chronic inflammation with enhanced hepcidin production.

Indexed as

AnemiaAnimalsAntimicrobial Cationic PeptidesBase SequenceCells, CulturedErythropoiesisErythropoietinFeasibility StudiesFemaleHepcidinsHumansHypoxia-Inducible Factor-Proline DioxygenasesInflammationLiverMaleMiceAntimicrobial Cationic PeptidesEgln1 protein, mouseErythropoietinHAMP protein, humanHamp protein, mouseHepcidinsHypoxia-Inducible Factor-Proline DioxygenasesPHD1 protein, mousePHD3 protein, mouseProcollagen-Proline DioxygenaseRNA, Small Interfering

Identifiers

PMID22611156
PMCPMC3433093
OpenAlexW2068256856

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.