Evidence map›Paper›PMID 19442620›Full record

ArticleBone2009

The bisphosphonate zoledronic acid decreases tumor growth in bone in mice with defective osteoclasts.

Angela C Hirbe, Anke J Roelofs, Desiree H Floyd, Hongju Deng, Stephanie N Becker, Lisa G Lanigan, Anthony J Apicelli, Zhiqiang Xu, Julie L Prior, Mark C Eagleton and 3 more

Open access · greenAbstract read
In one paragraph

Article in Bone, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 63 citations in OpenAlex.

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  19. Breast cancer cell targeting by prenylation inhibitors elucidated in living animals with a bioluminescence reporter.Clinical cancer research : an official journal of the American Association for Cancer Research · 2012
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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

13 authors at 6 institutions in 3 countries.

Angela C HirbeDepartment of Medicine, Division of Molecular Oncology, Washington University School of Medicine, St Louis, MO 63110, USA.
Anke J Roelofs
Desiree H Floyd
Hongju Deng
Stephanie N Becker
Lisa G Lanigan
Anthony J Apicelli
Zhiqiang Xu
Julie L Prior
Mark C Eagleton
David Piwnica-Worms
Michael J Rogers
Katherine Weilbaecher
Molecular Oncology (United States) · USWashington University in St. Louis · USImaging Center · USInstitute of Medical Sciences · INThe Ohio State University · USUniversity of Aberdeen · GB

Funding

Role of Inflammation in Tax-mediated TumorigenesisP01CA100730 · NCI · WASHINGTON UNIVERSITY · PI Malachi Griffith · 2003 to 2026
$44.8M
WU-MDACC Inter-Institutional Molecular Imaging CenterP50CA094056 · NCI · WASHINGTON UNIVERSITY · PI KOPAN, RAPHAEL · 2002 to 2016
$26.3M
PRE-AND POSTGRADUATE TRAINING IN MOLECULAR HEMATOLOGYT32HL007088 · NHLBI · WASHINGTON UNIVERSITY · PI Grant Anthony Challen, Stephen Oh · 1985 to 2026
$14.1M
ROLE OF BETA 3 INTEGRIN IN SKELETAL METASTASISR01CA097250 · NCI · WASHINGTON UNIVERSITY · PI WEILBAECHER, KATHERINE NELSON · 2003 to 2014
$3.3M
Cancer Research UK C13325/A7166NCI NIH HHS CA100730NCI NIH HHS P01 CA100730NCI NIH HHS P50 CA094056NCI NIH HHS P50 CA94056NCI NIH HHS R01 CA097250NHLBI NIH HHS T32 HL007088
6 · The paper itself

Abstract

Bisphosphonates (BPs), bone targeted drugs that disrupt osteoclast function, are routinely used to treat complications of bone metastasis. Studies in preclinical models of cancer have shown that BPs reduce skeletal tumor burden and increase survival. Similarly, we observed in the present study that administration of the Nitrogen-containing BP (N-BP), zoledronic acid (ZA) to osteolytic tumor-bearing Tax+ mice beginning at 6 months of age led to resolution of radiographic skeletal lesions. N-BPs inhibit farnesyl diphosphate (FPP) synthase, thereby inhibiting protein prenylation and causing cellular toxicity. We found that ZA decreased Tax+ tumor and B16 melanoma viability and caused the accumulation of unprenylated Rap1a proteins in vitro. However, it is presently unclear whether N-BPs exert anti-tumor effects in bone independent of inhibition of osteoclast (OC) function in vivo. Therefore, we evaluated the impact of treatment with ZA on B16 melanoma bone tumor burden in irradiated mice transplanted with splenic cells from src(-/-) mice, which have non-functioning OCs. OC-defective mice treated with ZA demonstrated a significant 88% decrease in tumor growth in bone compared to vehicle-treated OC-defective mice. These data support an osteoclast-independent role for N-BP therapy in bone metastasis.

Indexed as

AnimalsBone NeoplasmsCell Line, TumorCell SurvivalDiphosphonatesEnzyme ActivationGeranyltranstransferaseImidazolesMiceMice, Inbred C57BLMice, TransgenicNeoplasm MetastasisOsteoclastsProtein PrenylationZoledronic AcidDiphosphonatesGeranyltranstransferaseImidazolesZoledronic Acid

Identifiers

PMID19442620
PMCPMC2782613
OpenAlexW1976836551

What OpenQuestion holds

Textmetadata
LicenceTDM
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.