Evidence map›Paper›PMID 26722357›Full record

ArticleJournal of Cancer2016

Development of Soft Tissue Sarcomas in Ribosomal Proteins L5 and S24 Heterozygous Mice.

Shideh Kazerounian, Pedro D S C Ciarlini, Daniel Yuan, Roxanne Ghazvinian, Meritxell Alberich-Jorda, Mugdha Joshi, Hong Zhang, Alan H Beggs, Hanna T Gazda

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. The nucleolus, an ally, and an enemy of cancer cells.Histochemistry and cell biology · 2018
    Review
  11. Review
  12. How Ribosomes Translate Cancer.Cancer discovery · 2017
    Review
  13. Article
  14. Review
  15. Review
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 6 institutions in 2 countries.

Shideh Kazerounian1. Boston Children's Hospital, Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston, MA, USA ; 2. Harvard Medical School, Boston, MA, USA.
Pedro D S C Ciarlini3. University Hospitals Case Medical Center, Cleveland, OH, USA.
Daniel Yuan1. Boston Children's Hospital, Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston, MA, USA.
Roxanne Ghazvinian1. Boston Children's Hospital, Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston, MA, USA.
Meritxell Alberich-Jorda4. Institute of Molecular Genetics of the ASCR, Prague, Czech Republic.
Mugdha Joshi1. Boston Children's Hospital, Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston, MA, USA ; 2. Harvard Medical School, Boston, MA, USA.
Hong Zhang2. Harvard Medical School, Boston, MA, USA ; 5. Beth Israel Deaconess Medical Center, Hematology/Oncology Division, Boston, MA, USA.
Alan H Beggs1. Boston Children's Hospital, Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston, MA, USA ; 2. Harvard Medical School, Boston, MA, USA.
Hanna T Gazda1. Boston Children's Hospital, Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston, MA, USA ; 2. Harvard Medical School, Boston, MA, USA ; 6. Broad Institute, Cambridge, MA, USA.
Harvard University · USDana-Farber/Boston Children's Cancer and Blood Disorders Center · USBoston Children's Hospital · USBroad Institute · USCzech Academy of Sciences, Institute of Molecular Genetics · CZUniversity Hospitals Case Medical Center · US

Funding

New gene discoveries and biology of ribosomes in Diamond-Blackfan anemia.R01HL107558 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI GAZDA, HANNA TERESA · 2011 to 2014
$1.6M
New Gene Discoveries and Biology of Ribosomes in Diamond-Blackfan AnemiaK02HL111156 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI GAZDA, HANNA TERESA · 2012 to 2016
$568k
NHLBI NIH HHS K02 HL111156NHLBI NIH HHS R01 HL107558
6 · The paper itself

Abstract

Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome associated with ribosomal protein (RP) gene mutations. Recent studies have also demonstrated an increased risk of cancer predisposition among DBA patients. In this study, we report the formation of soft tissue sarcoma in the Rpl5 and Rps24 heterozygous mice. Our observation suggests that even though one wild-type allele of the Rpl5 or Rps24 gene prevents anemia in these mice, it still predisposes them to cancer development.

Indexed as

Diamond-Blackfan anemiaRibosomal proteins RPL5 and RPS24Rpl5 and Rps24 heterozygous miceSoft tissue sarcoma

Identifiers

PMID26722357
PMCPMC4679378
OpenAlexW2292986614

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.