Evidence map›Paper›PMID 22976955›Full record

ArticleBlood2012

Inactivation of ribosomal protein L22 promotes transformation by induction of the stemness factor, Lin28B.

Shuyun Rao, Sang-Yun Lee, Alejandro Gutierrez, Jacqueline Perrigoue, Roshan J Thapa, Zhigang Tu, John R Jeffers, Michele Rhodes, Stephen Anderson, Tamas Oravecz and 8 more

Open access · bronzeAbstract 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 103 papers.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed
3.8field-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

103 citing papers in PubMed, 153 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. 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
  11. Review
  12. Review
  13. Article
  14. Ribosome heterogeneity in development and disease.Frontiers in cell and developmental biology · 2024
    Article
  15. Article
  16. Shaping the host cell environment with viral noncoding RNAs.Seminars in cell & developmental biology · 2023
    Review
  17. Article
  18. Review
  19. Article
  20. Review

43 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

18 authors at 5 institutions in 1 country.

Shuyun RaoBlood Cell Development and Cancer Keystone, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Sang-Yun Lee
Alejandro Gutierrez
Jacqueline Perrigoue
Roshan J Thapa
Zhigang Tu
John R Jeffers
Michele Rhodes
Stephen Anderson
Tamas Oravecz
Stephen P Hunger
Roman A Timakhov
Rugang Zhang
Siddharth Balachandran
Gerard P Zambetti
Joseph R Testa
A Thomas Look
David L Wiest
Fox Chase Cancer Center · USDana-Farber Cancer Institute · USLexicon Pharmaceuticals (United States) · USSt. Jude Children's Research Hospital · USUniversity of Colorado Denver · US

Funding

COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Margaret von Mehren · 1985 to 2026
$138.8M
Children's Oncology Group Statistics &Data Center GrantU10CA098413 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI ANDERSON, JAMES R · 2003 to 2013
$67.5M
TRANSGENIC AND CHIMERIC MOUSE COREP30DK050306 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Ken Hashigiwa Cadwell · 1997 to 2026
$32.5M
Zebrafish Screens for Genetic Modifiers and Human Application in T-ALLP01CA068484 · NCI · DANA-FARBER CANCER INSTITUTE · PI ORKIN, STUART H · 1995 to 2010
$31.9M
Support for Human Specimen Banking in NCI-Supported Cancer Clinical TrialsU24CA114766 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI RAMIREZ MILAN, NILSA DEL CARMEN · 2005 to 2014
$14.5M
TRAINING PROGRAM IN CANCER RESEARCHT32CA009035 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI CHERNOFF, JONATHAN · 1985 to 2020
$10.5M
Basis for Lymphomagenesis in Akt2 Transgenic MiceR01CA077429 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI TESTA, JOSEPH R. · 1998 to 2013
$4.7M
Role of BRCA1 Pathway in Regulating Oncogene-Induced SenescenceR01CA160331 · NCI · WISTAR INSTITUTE · PI ZHANG, RUGANG · 2012 to 2021
$4.0M
Role of RPL22 in Thymocyte DevelopmentR01AI073920 · NIAID · RESEARCH INST OF FOX CHASE CAN CTR · PI WIEST, DAVID L. · 2007 to 2011
$2.1M
Zebrafish Chemical and Classical Genetics Approach to the Pathogenesis of T-ALLK08CA133103 · NCI · DANA-FARBER CANCER INST · PI GUTIERREZ, ALEJANDRO · 2008 to 2012
$705k
Rpl22 as Biomarker of Prognosis and Therapeutic Response in T-ALLR21CA141194 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI WIEST, DAVID L. · 2010 to 2011
$412k
NCI NIH HHS 5K08CA133103NCI NIH HHS 5P01CA068484NCI NIH HHS CA009035NCI NIH HHS K08 CA133103NCI NIH HHS P01 CA068484NCI NIH HHS P01CA06927NCI NIH HHS P30 CA006927NCI NIH HHS R01 CA077429NCI NIH HHS R01 CA160331NCI NIH HHS R01-CA77429NCI NIH HHS R21 CA141194NCI NIH HHS R21-CA141194NCI NIH HHS T32 CA009035NCI NIH HHS U10 CA098413NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA98413NCI NIH HHS U10 CA98543NCI NIH HHS U24 CA114766NIAID NIH HHS R01 AI073920NIAID NIH HHS R01-AI073920NIDDK NIH HHS P30 DK050306NIDDK NIH HHS P30-DK-50306
6 · The paper itself

Abstract

Ribosomal protein (RP) mutations in diseases such as 5q- syndrome both disrupt hematopoiesis and increase the risk of developing hematologic malignancy. However, the mechanism by which RP mutations increase cancer risk has remained an important unanswered question. We show here that monoallelic, germline inactivation of the ribosomal protein L22 (Rpl22) predisposes T-lineage progenitors to transformation. Indeed, RPL22 was found to be inactivated in ∼ 10% of human T-acute lymphoblastic leukemias. Moreover, monoallelic loss of Rpl22 accelerates development of thymic lymphoma in both a mouse model of T-cell malignancy and in acute transformation assays in vitro. We show that Rpl22 inactivation enhances transformation potential through induction of the stemness factor, Lin28B. Our finding that Rpl22 inactivation promotes transformation by inducing expression of Lin28B provides the first insight into the mechanistic basis by which mutations in Rpl22, and perhaps some other RP genes, increases cancer risk.

Indexed as

AnimalsCell Transformation, NeoplasticDNA-Binding ProteinsElectrophoretic Mobility Shift AssayFlow CytometryGene SilencingHematologic NeoplasmsHumansImmunoblottingMiceMice, TransgenicOligonucleotide Array Sequence AnalysisReal-Time Polymerase Chain ReactionRibosomal ProteinsRNA-Binding ProteinsT-LymphocytesDNA-Binding ProteinsLin28b protein, mouseRibosomal ProteinsRNA-Binding ProteinsRPL22 protein, mouse

Identifiers

PMID22976955
PMCPMC3488889
OpenAlexW2020574069

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.