Evidence map›Paper›PMID 24739392›Full record

ArticleMolecular cancer therapeutics2014

Targeting integrin α6 stimulates curative-type bone metastasis lesions in a xenograft model.

Terry H Landowski, Jaime Gard, Erika Pond, Gerald D Pond, Raymond B Nagle, Christopher P Geffre, Anne E Cress

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Integrin α6 Targeted Tumor Theranostics.Phenomics (Cham, Switzerland) · 2025
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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

7 authors at 1 institution in 1 country.

Terry H LandowskiAuthors' Affiliations: University of Arizona Cancer Center; Departments of Medicine, Medical Imaging, Pathology, and Cellular and Molecular Medicine, University of Arizona Cancer Center, Tucson, ArizonaAuthors' Affiliations: University of Arizona Cancer Center; Departments of Medicine, Medical Imaging, Pathology, and Cellular and Molecular Medicine, University of Arizona Cancer Center, Tucson, Arizona.
Jaime GardAuthors' Affiliations: University of Arizona Cancer Center; Departments of Medicine, Medical Imaging, Pathology, and Cellular and Molecular Medicine, University of Arizona Cancer Center, Tucson, Arizona.
Erika PondAuthors' Affiliations: University of Arizona Cancer Center; Departments of Medicine, Medical Imaging, Pathology, and Cellular and Molecular Medicine, University of Arizona Cancer Center, Tucson, Arizona.
Gerald D PondAuthors' Affiliations: University of Arizona Cancer Center; Departments of Medicine, Medical Imaging, Pathology, and Cellular and Molecular Medicine, University of Arizona Cancer Center, Tucson, Arizona.
Raymond B NagleAuthors' Affiliations: University of Arizona Cancer Center; Departments of Medicine, Medical Imaging, Pathology, and Cellular and Molecular Medicine, University of Arizona Cancer Center, Tucson, ArizonaAuthors' Affiliations: University of Arizona Cancer Center; Departments of Medicine, Medical Imaging, Pathology, and Cellular and Molecular Medicine, University of Arizona Cancer Center, Tucson, Arizona.
Christopher P GeffreAuthors' Affiliations: University of Arizona Cancer Center; Departments of Medicine, Medical Imaging, Pathology, and Cellular and Molecular Medicine, University of Arizona Cancer Center, Tucson, Arizona.
Anne E CressAuthors' Affiliations: University of Arizona Cancer Center; Departments of Medicine, Medical Imaging, Pathology, and Cellular and Molecular Medicine, University of Arizona Cancer Center, Tucson, ArizonaAuthors' Affiliations: University of Arizona Cancer Center; Departments of Medicine, Medical Imaging, Pathology, and Cellular and Molecular Medicine, University of Arizona Cancer Center, Tucson, Arizona cress@email.arizona.edu.
University of Arizona · US

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Dan Theodorescu · 1985 to 2026
$110.2M
Therapeutic Targeting of Hypoxic and Oxidative StressP01CA017094 · NCI · UNIVERSITY OF ARIZONA · PI GILLIES, ROBERT J. · 1985 to 2011
$13.7M
Human Prostate Cancer Metastasis and Laminin Binding IntegrinsR01CA159406 · NCI · UNIVERSITY OF ARIZONA · PI CRESS, ANNE E · 2011 to 2015
$1.5M
NCI NIH HHS P01 CA017094NCI NIH HHS P30 CA023074NCI NIH HHS R01 CA159406
6 · The paper itself

Abstract

Laminin-binding integrin receptors are key mediators of epithelial cell migration and tumor metastasis. Recent studies have demonstrated a role for the α6 integrin (ITGA6/CD49f) in maintaining stem cell compartments within normal bone marrow and in residency of tumors metastatic to bone. In this study, we tested a function-blocking antibody specific for ITGA6, called J8H, to determine if preexisting cancer lesions in bone could be slowed and/or animal survival improved. Human prostate tumors were established by intracardiac injection into male SCID mice and treatment with J8H antibody was initiated after 1 week. Tumor progression was monitored by micro-computed tomography (CT) imaging of skeletal lesions. Animals that received weekly injections of the anti-ITGA6 antibody showed radiographic progression in only 40% of osseous tumors (femur or tibia), compared with control animals, where 80% of the lesions (femur or tibia) showed progression at 5 weeks. Kaplan-Meier survival analysis demonstrated a significant survival advantage for J8H-treated animals. Unexpectedly, CT image analysis revealed an increased proportion of bone lesions displaying a sclerotic rim of new bone formation, encapsulating the arrested lytic lesions in animals that received the anti-ITGA6 antibody treatment. Histopathology of the sclerotic lesions demonstrated well-circumscribed tumor within bone, surrounded by fibrosis. These data suggest that systemic targeting of the ITGA6-dependent function of established tumors in bone may offer a noncytotoxic approach to arrest the osteolytic progression of metastatic prostate cancer, thereby providing a new therapeutic strategy for advanced disease.

Indexed as

Molecular Targeted TherapyAnimalsAntibodiesAntibodies, Monoclonal, Murine-DerivedBone NeoplasmsCell Line, TumorHumansIntegrin alpha6MaleMiceOsteoblastsProstatic NeoplasmsXenograft Model Antitumor AssaysAntibodiesAntibodies, Monoclonal, Murine-DerivedIntegrin alpha6

Identifiers

PMID24739392
PMCPMC4069206
OpenAlexW2099634036

What OpenQuestion holds

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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.