Evidence map›Paper›PMID 28264936›Full record

ArticleEMBO molecular medicine2017

Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with

Ram Ajore, David Raiser, Marie McConkey, Magnus Jöud, Bernd Boidol, Brenton Mar, Gordon Saksena, David M Weinstock, Scott Armstrong, Steven R Ellis and 2 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

75 citing papers in PubMed, 102 citations in OpenAlex.

  1. Article
  2. Review
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  4. Science advances · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Ribosome specialization by cancer-associated ribosomal protein mutations: progress made and open questions.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  12. Article
  13. Review
  14. Deficiency ofInternational journal of molecular sciences · 2024
    Article
  15. Article
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  18. Article
  19. Review
  20. Article

15 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

12 authors at 6 institutions in 2 countries.

Ram AjoreHematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden.
David RaiserDepartment of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Marie McConkeyDepartment of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Magnus JöudHematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Bernd BoidolDepartment of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Brenton MarDepartment of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Gordon SaksenaBroad Institute, 7 Cambridge Center, Cambridge, MA, USA.
David M WeinstockDana-Farber Cancer Institute, Boston, MA, USA.
Scott ArmstrongMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Steven R EllisDepartment of Biochemistry and Molecular Biology, University of Louisville, Louisville, KY, USA.
Benjamin L EbertDepartment of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA benjamin_ebert@dfci.harvard.edu bjorn.nilsson@med.lu.se.
Björn NilssonHematology and Transfusion Medicine, Department of Laboratory Medicine, Lund University, Lund, Sweden benjamin_ebert@dfci.harvard.edu bjorn.nilsson@med.lu.se.ORCID 0000-0001-5542-0254
Brigham and Women's Hospital · USBroad Institute · USLund University · SEDana-Farber Cancer Institute · USMemorial Sloan Kettering Cancer Center · USUniversity of Louisville · US

Funding

TYROSINE KINASE ONCOGENESIS IN MYELOID LEUKEMIAP01CA066996 · NCI · DANA-FARBER CANCER INSTITUTE · PI SCOTT A ARMSTRONG · 1996 to 2026
$52.5M
Targeting SYK Kinase in AMLP50CA206963 · NCI · DANA-FARBER CANCER INST · PI ASTER, JON C. · 2017 to 2021
$10.6M
Tyrosine Kinases, Serine-Threonine Kinases,&Phosophatases in PathogenesisP01CA108631 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ESTEY, ELIHU · 2005 to 2009
$9.7M
Functional Genomic Dissection of Refractory AnemiaR01HL082945 · NHLBI · DANA-FARBER CANCER INSTITUTE · PI EBERT, BENJAMIN LEVINE · 2005 to 2022
$6.8M
NCI NIH HHS P01 CA066996NCI NIH HHS P01 CA108631NCI NIH HHS P50 CA206963NHLBI NIH HHS R01 HL082945
6 · The paper itself

Abstract

Heterozygous inactivating mutations in ribosomal protein genes (RPGs) are associated with hematopoietic and developmental abnormalities, activation of p53, and altered risk of cancer in humans and model organisms. Here we performed a large-scale analysis of cancer genome data to examine the frequency and selective pressure of RPG lesions across human cancers. We found that hemizygous RPG deletions are common, occurring in about 43% of 10,744 cancer specimens and cell lines. Consistent with p53-dependent negative selection, such lesions are underrepresented in

Indexed as

Gene DeletionMutationCell Line, TumorGene Expression Regulation, NeoplasticHumansNeoplasmsRibosomal ProteinsTumor Suppressor Protein p53Ribosomal ProteinsTP53 protein, humanTumor Suppressor Protein p53cancerribosomal gene haploinsufficiencyribosome function

Identifiers

PMID28264936
PMCPMC5376749
OpenAlexW2592715362

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.