Evidence map›Paper›PMID 17311992›Full record

ArticleBlood2007

Development of a murine model for blastoid variant mantle-cell lymphoma.

Richard J Ford, Long Shen, Yen Chiu Lin-Lee, Lan V Pham, Asha Multani, Hai-Jun Zhou, Archito T Tamayo, ChongJie Zhang, Lesleyann Hawthorn, John K Cowell and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 38 citations in OpenAlex.

  1. 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
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  8. NKT Cell Responses to B Cell Lymphoma.Medical sciences (Basel, Switzerland) · 2014
    Article
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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

11 authors at 6 institutions in 2 countries.

Richard J FordDepartment of Hematopathology, University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Long Shen
Yen Chiu Lin-Lee
Lan V Pham
Asha Multani
Hai-Jun Zhou
Archito T Tamayo
ChongJie Zhang
Lesleyann Hawthorn
John K Cowell
Julian L Ambrus
The University of Texas MD Anderson Cancer Center · USCancer Genetics (United States) · USKaleida Health · USRoswell Park Comprehensive Cancer Center · USUniversity at Buffalo, State University of New York · USWomen & Children's Hospital of Buffalo · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Positive and Negative Regulatory Pathways In LymphomaR01CA100836 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI FORD, RICHARD J · 2003 to 2007
$1.6M
NCI NIH HHS CA 16672-26NCI NIH HHS P30 CA016672NCI NIH HHS R01 CA 100836
6 · The paper itself

Abstract

Blastoid-variant mantle-cell lymphoma (MCL-BV), unlike most B-cell non-Hodgkin lymphomas (NHL-Bs), is refractory to conventional chemotherapy and associated with a very poor prognosis. Development of new therapies has been hampered by the lack of valid animal models. We have developed a novel murine model of MCL-BV by crossing interleukin 14alpha (IL-14alpha) transgenic mice with c-Myc transgenic mice (double transgenic [DTG]). IL-14alpha is a B-cell growth factor that is expressed in a number of high-grade lymphomas, including MCL-BV. Ninety-five percent of IL-14alpha transgenic mice develop CD5(+) large B-cell lymphomas by 18 months of age. Sixty percent of c-Myc transgenic mice develop pre-B-cell lymphomas by 12 months of age. Close to 100% of DTG mice develop an aggressive, rapidly fatal lymphoma at 3 to 4 months of age that is CD5(+), CD19(+), CD21(-), CD23(-), sIgM(+). The tumor is found in the blood, bone marrow, liver, spleen, lymph nodes, gastrointestinal tract, and lungs and rarely in the brain, similar to the involvement seen in human MCL-BV. Immunoglobulin gene rearrangements document the monoclonality of the tumor. Cyclin D1 is highly expressed in these tumors, as it is in MCL-BV. DTG represents a novel model for MCL-BV that should reveal important insights into the pathogenesis of the lymphoma and contribute to the development of new forms of therapy.

Indexed as

Disease Models, AnimalAnimalsB-LymphocytesGene Expression Regulation, NeoplasticGene RearrangementImmunoglobulinsKaryotypingLymphoma, Mantle-CellMiceMice, Inbred C57BLMice, SCIDMice, TransgenicNF-kappa BProto-Oncogene Proteins c-mycReceptors, InterleukinImmunoglobulinsinterleukin-14 receptorNF-kappa BProto-Oncogene Proteins c-mycReceptors, Interleukin

Identifiers

PMID17311992
PMCPMC1885517
OpenAlexW2036241887

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.