Evidence map›Paper›PMID 23079656›Full record

ArticleCancer cell2012

Therapeutic targeting of the cyclin D3:CDK4/6 complex in T cell leukemia.

Catherine M Sawai, Jacquelyn Freund, Philmo Oh, Delphine Ndiaye-Lobry, Jamieson C Bretz, Alexandros Strikoudis, Lali Genesca, Thomas Trimarchi, Michelle A Kelliher, Marcus Clark and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

115 citing papers in PubMed, 180 citations in OpenAlex.

  1. Article
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  4. Review
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  16. Review
  17. Review
  18. Article
  19. Targeting CDK4 and CDK6 in cancer.Nature reviews. Cancer · 2022
    Review
  20. Article

55 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

13 authors at 5 institutions in 2 countries.

Catherine M SawaiDepartment of Pathology and Howard Hughes Medical Institute, New York University School of Medicine, New York, NY 10016, USA.
Jacquelyn Freund
Philmo Oh
Delphine Ndiaye-Lobry
Jamieson C Bretz
Alexandros Strikoudis
Lali Genesca
Thomas Trimarchi
Michelle A Kelliher
Marcus Clark
Jean Soulier
Selina Chen-Kiang
Iannis Aifantis
Howard Hughes Medical Institute · USCornell University · USInserm · FRUniversity of Chicago · USUniversity of Massachusetts Chan Medical School · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Mechanism(s) of TAL-1/SCL-mediated LeukemogenesisR01CA096899 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MICHELLE ALICE KELLIHER · 2004 to 2026
$6.9M
The role of the SCF/FBW7 ubiquitin ligase complex in hematopiesis and leukemia.R01CA133379 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AIFANTIS, IANNIS · 2009 to 2018
$3.6M
Regulation of hematopoietic stem cell differentiationR01CA105129 · NCI · UNIVERSITY OF CHICAGO · PI AIFANTIS, IANNIS · 2005 to 2014
$2.8M
Mechanisms of T cell leukemia induction and maintenanceR01CA149655 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AIFANTIS, IANNIS · 2010 to 2015
$2.0M
Regulation of cyclin D3 in B lymphocyte developmentR01GM088847 · NIGMS · UNIVERSITY OF CHICAGO · PI CLARK, MARCUS RAMSAY · 2010 to 2013
$1.2M
Modifiers of Notch stability and their role in cancerR21CA141399 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AIFANTIS, IANNIS, HUBBARD, E. JANE ALBERT · 2010 to 2011
$399k
Howard Hughes Medical InstituteNCI NIH HHS 5 P30CA16087-31NCI NIH HHS 5P30CA16087-31NCI NIH HHS P30 CA016087NCI NIH HHS P30 CA016087-30NCI NIH HHS R01 CA096899NCI NIH HHS R01 CA105129NCI NIH HHS R01CA105129NCI NIH HHS R01 CA133379NCI NIH HHS R01CA133379NCI NIH HHS R01 CA149655NCI NIH HHS R01CA149655NCI NIH HHS R21 CA141399NCI NIH HHS R21CA141399NIGMS NIH HHS R01 GM088847NIGMS NIH HHS R01GM088847
6 · The paper itself

Abstract

D-type cyclins form complexes with cyclin-dependent kinases (CDK4/6) and promote cell cycle progression. Although cyclin D functions appear largely tissue specific, we demonstrate that cyclin D3 has unique functions in lymphocyte development and cannot be replaced by cyclin D2, which is also expressed during blood differentiation. We show that only combined deletion of p27(Kip1) and retinoblastoma tumor suppressor (Rb) is sufficient to rescue the development of Ccnd3(-/-) thymocytes. Furthermore, we show that a small molecule targeting the kinase function of cyclin D3:CDK4/6 inhibits both cell cycle entry in human T cell acute lymphoblastic leukemia (T-ALL) and disease progression in animal models of T-ALL. These studies identify unique functions for cyclin D3:CDK4/6 complexes and suggest potential therapeutic protocols for this devastating blood tumor.

Indexed as

AnimalsCyclin D2Cyclin D3Cyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Cyclin-Dependent Kinase Inhibitor p27HumansLymphocytesMicePrecursor T-Cell Lymphoblastic Leukemia-LymphomaReceptor, Notch1Retinoblastoma ProteinCyclin D2Cyclin D3Cyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Cyclin-Dependent Kinase Inhibitor p27Receptor, Notch1Retinoblastoma Protein

Identifiers

PMID23079656
PMCPMC3493168
OpenAlexW2087374769

What OpenQuestion holds

Textmetadata
LicenceTDM
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.