Evidence map›Paper›PMID 25779950›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2015

Targeting IL11 Receptor in Leukemia and Lymphoma: A Functional Ligand-Directed Study and Hematopathology Analysis of Patient-Derived Specimens.

Katja Karjalainen, Diana E Jaalouk, Carlos Bueso-Ramos, Laura Bover, Yan Sun, Akihiko Kuniyasu, Wouter H P Driessen, Marina Cardó-Vila, Cecilia Rietz, Amado J Zurita and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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  8. BMTP-11 is active in preclinical models of human osteosarcoma and a candidate targeted drug for clinical translation.Proceedings of the National Academy of Sciences of the United States of America · 2017
    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

17 authors at 6 institutions in 5 countries.

Katja KarjalainenDepartment of Experimental Therapeutics, The University of Texas M.D. Anderson Cancer Center, Houston, Texas. Department of Biological and Environmental Science, The University of Helsinki, Helsinki, Finland.
Diana E JaaloukDepartment of Biology, American University of Beirut, Beirut, Lebanon.
Carlos Bueso-RamosDepartment of Hematopathology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Laura BoverDepartment of Genomic Medicine, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Yan SunDepartment of Cancer Systems Imaging, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Akihiko KuniyasuDepartment of Molecular Cell Pharmacology, Sojo University, Kumamoto, Japan.
Wouter H P DriessenRoche, Basel, Switzerland.
Marina Cardó-VilaUniversity of New Mexico Cancer Center, University of New Mexico School of Medicine, Albuquerque, New Mexico. Division of Molecular Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico.
Cecilia RietzUniversity of New Mexico Cancer Center, University of New Mexico School of Medicine, Albuquerque, New Mexico. Division of Molecular Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico.
Amado J ZuritaDepartment of Genitourinary Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Susan O'BrienDepartment of Leukemia, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Hagop M KantarjianDepartment of Leukemia, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Jorge E CortesDepartment of Leukemia, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
George A CalinDepartment of Experimental Therapeutics, The University of Texas M.D. Anderson Cancer Center, Houston, Texas. Department of Leukemia, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Erkki KoivunenDepartment of Biological and Environmental Science, The University of Helsinki, Helsinki, Finland. Department of Leukemia, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Wadih ArapUniversity of New Mexico Cancer Center, University of New Mexico School of Medicine, Albuquerque, New Mexico. Division of Hematology/Oncology, Department of Internal Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico. rpasqual@salud.unm.edu warap@salud.unm.edu.
Renata PasqualiniUniversity of New Mexico Cancer Center, University of New Mexico School of Medicine, Albuquerque, New Mexico. Division of Molecular Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico. rpasqual@salud.unm.edu warap@salud.unm.edu.
The University of Texas MD Anderson Cancer Center · USUniversity of New Mexico · USUniversity of Helsinki · FIAmerican University of Beirut · LBRoche (Switzerland) · CHSojo University · JP

Funding

University of Texas M.D. Anderson Cancer SPORE-LeukemiaP50CA100632 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KONOPLEVA, MARINA Y · 2003 to 2023
$43.7M
NCI NIH HHS P50 CA100632
6 · The paper itself

Abstract

purposeThe IL11 receptor (IL11R) is an established molecular target in primary tumors of bone, such as osteosarcoma, and in secondary bone metastases from solid tumors, such as prostate cancer. However, its potential role in management of hematopoietic malignancies has not yet been determined. Here, we evaluated the IL11R as a candidate therapeutic target in human leukemia and lymphoma. EXPERIMENTAL DESIGN AND

resultsFirst, we show that the IL11R protein is expressed in a variety of human leukemia- and lymphoma-derived cell lines and in a large panel of bone marrow samples from leukemia and lymphoma patients, whereas expression is absent from nonmalignant control bone marrow. Moreover, a targeted peptidomimetic prototype (termed BMTP-11), specifically bound to leukemia and lymphoma cell membranes, induced ligand-receptor internalization mediated by the IL11R, and resulted in a specific dose-dependent cell death induction in these cells. Finally, a pilot drug lead-optimization program yielded a new myristoylated BMTP-11 analogue with an apparent improved antileukemia cell profile.

conclusionsThese results indicate (i) that the IL11R is a suitable cell surface target for ligand-directed applications in human leukemia and lymphoma and (ii) that BMTP-11 and its derivatives have translational potential against this group of malignant diseases.

Indexed as

Amino Acid SequenceAntineoplastic AgentsCell Line, TumorCell SurvivalDrug Screening Assays, AntitumorHumansInhibitory Concentration 50LeukemiaLigandsLymphomaMolecular Sequence DataPeptidesReceptors, Interleukin-11Antineoplastic Agentsbone metastasis-targeting peptidomimetic-11LigandsPeptidesReceptors, Interleukin-11

Identifiers

PMID25779950
PMCPMC4490100
OpenAlexW2120708197

What OpenQuestion holds

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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.