Evidence map›Paper›PMID 20826722›Full record

ArticleBlood2010

Fancd2-/- mice have hematopoietic defects that can be partially corrected by resveratrol.

Qing-Shuo Zhang, Laura Marquez-Loza, Laura Eaton, Andrew W Duncan, Devorah C Goldman, Praveen Anur, Kevin Watanabe-Smith, R Keaney Rathbun, William H Fleming, Grover C Bagby and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
3.6field-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

63 citing papers in PubMed, 101 citations in OpenAlex.

  1. Trial
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  8. Dynamic Tracking of Native Precursors in Adult Mice.bioRxiv : the preprint server for biology · 2024
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Mechanisms involved in hematopoietic stem cell aging.Cellular and molecular life sciences : CMLS · 2022
    Review
  14. Review
  15. Review
  16. DNA damage and repair in the hematopoietic system.Acta biochimica et biophysica Sinica · 2022
    Review
  17. Article
  18. Review
  19. Article
  20. Article

3 more citing papers are in PubMed but not listed here.

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

11 authors at 2 institutions in 1 country.

Qing-Shuo ZhangOregon Stem Cell Center, Department of Pediatrics, Oregon Health & Science University, Portland, OR, USA. zhangqi@ohsu.edu
Laura Marquez-Loza
Laura Eaton
Andrew W Duncan
Devorah C Goldman
Praveen Anur
Kevin Watanabe-Smith
R Keaney Rathbun
William H Fleming
Grover C Bagby
Markus Grompe
Oregon Health & Science University · USPortland VA Medical Center · US

Funding

Xenograft CoreP01HL048546 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI FLEMING, WILLIAM H · 1994 to 2020
$36.4M
Program in Molecular and Cellular BiosciencesT32GM071338 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI MASLEN, CHERYL L · 2005 to 2020
$3.5M
Stem Cell Plasticity of Adult Vascular TissueR01HL069133 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI FLEMING, WILLIAM H · 2001 to 2011
$2.8M
Fanconi Anemia stem cells allow molecular characterization of acute leukemiaR01CA138237 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI BAGBY, GROVER CARLTON, CLAPP, DAVID W · 2008 to 2012
$1.9M
Endothelial Potential of Bone Marrow Derived ProgenitorsR01HL077818 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI FLEMING, WILLIAM H · 2005 to 2008
$1.2M
NCI NIH HHS 1R01CA138237NCI NIH HHS R01 CA138237NHLBI NIH HHS 1P01HL48546NHLBI NIH HHS HL069133NHLBI NIH HHS HL077818NHLBI NIH HHS P01 HL048546NHLBI NIH HHS R01 HL069133NHLBI NIH HHS R01 HL077818NIGMS NIH HHS T32 GM071338
6 · The paper itself

Abstract

Progressive bone marrow failure is a major cause of morbidity and mortality in human Fanconi Anemia patients. In an effort to develop a Fanconi Anemia murine model to study bone marrow failure, we found that Fancd2(-/-) mice have readily measurable hematopoietic defects. Fancd2 deficiency was associated with a significant decline in the size of the c-Kit(+)Sca-1(+)Lineage(-) (KSL) pool and reduced stem cell repopulation and spleen colony-forming capacity. Fancd2(-/-) KSL cells showed an abnormal cell cycle status and loss of quiescence. In addition, the supportive function of the marrow microenvironment was compromised in Fancd2(-/-) mice. Treatment with Sirt1-mimetic and the antioxidant drug, resveratrol, maintained Fancd2(-/-) KSL cells in quiescence, improved the marrow microenvironment, partially corrected the abnormal cell cycle status, and significantly improved the spleen colony-forming capacity of Fancd2(-/-) bone marrow cells. We conclude that Fancd2(-/-) mice have readily quantifiable hematopoietic defects, and that this model is well suited for pharmacologic screening studies.

Indexed as

AnimalsAntioxidantsBone MarrowCell CycleCell LineageColony-Forming Units AssayFanconi AnemiaFanconi Anemia Complementation Group D2 ProteinHematopoietic Stem CellsHematopoietic SystemMiceMice, KnockoutMice, TransgenicResveratrolSpleenStilbenesAntioxidantsFancd2 protein, mouseFanconi Anemia Complementation Group D2 ProteinResveratrolStilbenes

Identifiers

PMID20826722
PMCPMC3012535
OpenAlexW1972104861

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.