Evidence map›Paper›PMID 27317903›Full record

ArticleThe American journal of pathology2016

Interleukin-11 Receptor Is a Candidate Target for Ligand-Directed Therapy in Lung Cancer: Analysis of Clinical Samples and BMTP-11 Preclinical Activity.

Marina Cardó-Vila, Serena Marchiò, Masanori Sato, Fernanda I Staquicini, Tracey L Smith, Julianna K Bronk, Guosheng Yin, Amado J Zurita, Menghong Sun, Carmen Behrens and 6 more

Open access · hybridAbstract read
In one paragraph

Article in The American journal of pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. The role of IL-11 in chronic diseases.Frontiers in immunology · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Interleukin-11 receptor subunit α-1 is required for maximal airway responsiveness to methacholine after acute exposure to ozone.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Article
  9. Review
  10. Review
  11. Bazedoxifene as a novel GP130 inhibitor for Colon Cancer therapy.Journal of experimental & clinical cancer research : CR · 2019
    Article
  12. Article
  13. Article
  14. 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
  15. Article
  16. Article
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

16 authors at 6 institutions in 4 countries.

Marina Cardó-VilaUniversity of New Mexico Comprehensive 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; Department of Internal Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico.
Serena MarchiòUniversity of New Mexico Comprehensive 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; Department of Internal Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico; Department of Oncology, University of Turin, Turin, Italy; Candiolo Cancer Institute-IRCCS, Candiolo, Italy.
Masanori SatoFirst Surgery Department, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Fernanda I StaquiciniUniversity of New Mexico Comprehensive 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; Department of Internal Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico.
Tracey L SmithUniversity of New Mexico Comprehensive 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; Department of Internal Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico.
Julianna K BronkDepartment of Genitourinary Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Guosheng YinDepartment of Biostatistics, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Amado J ZuritaDepartment of Genitourinary Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Menghong SunTissue Bank and Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.
Carmen BehrensDepartment of Thoracic/Head and Neck Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Richard L SidmanDepartment of Neurology, Harvard Medical School and Beth Israel Deaconess Medical Center, Boston, Massachusetts.
J Jack LeeDepartment of Biostatistics, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Waun K HongDivision of Cancer Medicine, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Ignacio I WistubaDepartment of Translational Molecular Pathology, The University of Texas M.D. Anderson Cancer Center, Houston, Texas.
Wadih ArapUniversity of New Mexico Comprehensive Cancer Center, University of New Mexico School of Medicine, Albuquerque, New Mexico; Department of Internal Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico; Division of Hematology/Oncology, University of New Mexico School of Medicine, Albuquerque, New Mexico. Electronic address: warap@salud.unm.edu.
Renata PasqualiniUniversity of New Mexico Comprehensive 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; Department of Internal Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico. Electronic address: rpasqual@salud.unm.edu.
The University of Texas MD Anderson Cancer Center · USUNM Comprehensive Cancer CenterBeth Israel Deaconess Medical Center · USFudan University Shanghai Cancer Center · CNHamamatsu University School of Medicine · JPNew Mexico Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GIBBONS, DON LYNN · 1996 to 2024
$57.4M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA070907
6 · The paper itself

Abstract

We previously isolated an IL-11-mimic motif (CGRRAGGSC) that binds to IL-11 receptor (IL-11R) in vitro and accumulates in IL-11R-expressing tumors in vivo. This synthetic peptide ligand was used as a tumor-targeting moiety in the rational design of BMTP-11, which is a drug candidate in clinical trials. Here, we investigated the specificity and accessibility of IL-11R as a target and the efficacy of BMTP-11 as a ligand-targeted drug in lung cancer. We observed high IL-11R expression levels in a large cohort of patients (n = 368). In matching surgical specimens (i.e., paired tumors and nonmalignant tissues), the cytoplasmic levels of IL-11R in tumor areas were significantly higher than in nonmalignant tissues (n = 36; P = 0.003). Notably, marked overexpression of IL-11R was observed in both tumor epithelial and vascular endothelial cell membranes (n = 301; P < 0.0001). BMTP-11 induced in vitro cell death in a representative panel of human lung cancer cell lines. BMTP-11 treatment attenuated the growth of subcutaneous xenografts and reduced the number of pulmonary tumors after tail vein injection of human lung cancer cells in mice. Our findings validate BMTP-11 as a pharmacologic candidate drug in preclinical models of lung cancer and patient-derived tumors. Moreover, the high expression level in patients with non-small cell lung cancer is a promising feature for potential translational applications.

Indexed as

AnimalsAntineoplastic AgentsApoptosisBiomarkers, TumorCarcinomaCell Line, TumorCell ProliferationCell SurvivalFemaleFlow CytometryHumansImmunohistochemistryLung NeoplasmsMaleMiceMice, Inbred BALB CAntineoplastic AgentsBiomarkers, Tumorbone metastasis-targeting peptidomimetic-11PeptidesReceptors, Interleukin-11

Identifiers

PMID27317903
PMCPMC4973658
OpenAlexW2427452406

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.