Evidence map›Paper›PMID 24352880›Full record

ArticleBlood2014

Mantle cell lymphoma in cyclin D1 transgenic mice with Bim-deficient B cells.

Samuel G Katz, James L Labelle, Hailong Meng, Regina P Valeriano, Jill K Fisher, Heather Sun, Scott J Rodig, Steven H Kleinstein, Loren D Walensky

Abstract read
In one paragraph

Article in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

25 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. The Novel Immunocompetent Eµ-SOX11CCND1 Mouse Model Phenotypically and Molecularly Resembles Human Mantle Cell Lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  3. Review
  4. Article
  5. Mouse Models in the Study of Mature B-Cell Malignancies.Cold Spring Harbor perspectives in medicine · 2021
    Review
  6. Article
  7. Review
  8. Article
  9. Cell Death Pathways in Lymphoid Malignancies.Current oncology reports · 2020
    Review
  10. Article
  11. Advances in Molecular Biology and Targeted Therapy of Mantle Cell Lymphoma.International journal of molecular sciences · 2019
    Review
  12. Article
  13. Review
  14. Observational
  15. Development and Significance of Mouse Models in Lymphoma Research.Current hematologic malignancy reports · 2019
    Review
  16. Article
  17. Article
  18. Measurement of BH3-only protein tolerance.Cell death and differentiation · 2018
    Article
  19. FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  20. 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 3 institutions in 1 country.

Samuel G KatzDepartment of Pediatric Oncology and the Linde Program in Cancer Chemical Biology, Dana-Farber Cancer Institute, Boston, MA;
James L Labelle
Hailong Meng
Regina P Valeriano
Jill K Fisher
Heather Sun
Scott J Rodig
Steven H Kleinstein
Loren D Walensky
Dana-Farber Cancer Institute · USHarvard University · USYale University · US

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI A. Heather Eliassen · 1985 to 2026
$330.6M
Pathologic BIM Suppression & Pharmacologic BH3 Replacement in B-Cell LymphomaK08CA151450 · NCI · UNIVERSITY OF CHICAGO · PI LABELLE, JAMES LAURENCE · 2011 to 2015
$842k
NCI NIH HHS 5 P30CA06516NCI NIH HHS K08 CA151450NCI NIH HHS P30 CA006516
6 · The paper itself

Abstract

Mantle cell lymphoma (MCL) is a highly aggressive B-cell lymphoma resistant to conventional chemotherapy. Although defined by the characteristic t(11;14) translocation, MCL has not been recapitulated in transgenic mouse models of cyclin D1 overexpression alone. Indeed, several genetic aberrations have been identified in MCL that may contribute to its pathogenesis and chemoresistance. Of particular interest is the frequent biallelic deletion of the proapoptotic BCL-2 family protein BIM. BIM exerts its pro-death function via its α-helical BH3 death domain that has the dual capacity to inhibit antiapoptotic proteins such as BCL-2 and MCL-1 and directly trigger proapoptotic proteins such as the mitochondrial executioner protein BAX. To evaluate a functional role for Bim deletion in the pathogenesis of MCL, we generated cyclin D1-transgenic mice harboring Bim-deficient B cells. In response to immunization, Eμ(CycD1)CD19(CRE)Bim(fl/fl) mice manifested selective expansion of their splenic mantle zone compartment. Three distinct immune stimulation regimens induced lymphomas with histopathologic and molecular features of human MCL in a subset of mice. Thus, deletion of Bim in B cells, in the context of cyclin D1 overexpression, disrupts a critical control point in lymphoid maturation and predisposes to the development of MCL. This genetic proof of concept for MCL pathogenesis suggests an opportunity to reactivate the death pathway by pharmacologic mimicry of proapoptotic BIM.

Indexed as

AnimalsApoptosis Regulatory ProteinsBcl-2-Like Protein 11B-LymphocytesCell CycleCyclin D1FemaleFlow CytometryHumansImmunoenzyme TechniquesImmunophenotypingLymphoma, Mantle-CellMaleMembrane ProteinsMiceMice, Inbred C57BLApoptosis Regulatory ProteinsBCL2L11 protein, humanBcl2l11 protein, mouseBcl-2-Like Protein 11Ccnd1 protein, mouseCyclin D1Membrane ProteinsProto-Oncogene Proteins

Identifiers

PMID24352880
PMCPMC3916879
OpenAlexW2065799492

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.