Evidence map›Paper›PMID 25287160›Full record

ArticleCancer research2014

NGF blockade at early times during bone cancer development attenuates bone destruction and increases limb use.

Gwen McCaffrey, Michelle L Thompson, Lisa Majuta, Michelle N Fealk, Stephane Chartier, Geraldine Longo, Patrick W Mantyh

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
5.3field-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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Tumor Innervation: From Bystander to Emerging Therapeutic Target for Cancer.International journal of molecular sciences · 2025
    Review
  9. Review
  10. Article
  11. Review
  12. Effect of chronic stress on tumorigenesis and development.Cellular and molecular life sciences : CMLS · 2022
    Review
  13. Mechanisms of cancer pain.Frontiers in pain research (Lausanne, Switzerland) · 2022
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Nerves in the Tumor Microenvironment: Origin and Effects.Frontiers in cell and developmental biology · 2020
    Review
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.

Gwen McCaffreyDepartment of Pharmacology, University of Arizona College of Medicine, Tucson, Arizona.
Michelle L ThompsonDepartment of Pharmacology, University of Arizona College of Medicine, Tucson, Arizona.
Lisa MajutaDepartment of Pharmacology, University of Arizona College of Medicine, Tucson, Arizona.
Michelle N FealkDepartment of Pharmacology, University of Arizona College of Medicine, Tucson, Arizona.
Stephane ChartierDepartment of Pharmacology, University of Arizona College of Medicine, Tucson, Arizona.
Geraldine LongoDepartment of Pharmacology, University of Arizona College of Medicine, Tucson, Arizona.
Patrick W MantyhDepartment of Pharmacology, University of Arizona College of Medicine, Tucson, Arizona. pmantyh@email.arizona.edu.
University of Arizona · US

Funding

Peripheral Nociceptors in Persistent PainR01NS023970 · NINDS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MANTYH, PATRICK WILLIAM · 1987 to 2019
$3.7M
PERIPHERAL NOCICEPTORS IN PERSISTENT PAINR37NS023970 · NINDS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MANTYH, PATRICK WILLIAM · 2001 to 2007
$2.9M
Preventive Analgesia for Bone Cancer PainR01CA154550 · NCI · UNIVERSITY OF ARIZONA · PI MANTYH, PATRICK WILLIAM · 2011 to 2015
$1.6M
METASTATIC PROSTATE CANCER-INDUCED BONE PAINR01CA157449 · NCI · UNIVERSITY OF ARIZONA · PI MANTYH, PATRICK WILLIAM · 2011 to 2015
$1.5M
NCI NIH HHS CA154550NCI NIH HHS R01 CA154550NCI NIH HHS R01 CA157449NINDS NIH HHS NS023970NINDS NIH HHS R01 NS023970NINDS NIH HHS R37 NS023970
6 · The paper itself

Abstract

Studies in animals and humans show that blockade of nerve growth factor (NGF) attenuates both malignant and nonmalignant skeletal pain. While reduction of pain is important, a largely unanswered question is what other benefits NGF blockade might confer in patients with bone cancer. Using a mouse graft model of bone sarcoma, we demonstrate that early treatment with an NGF antibody reduced tumor-induced bone destruction, delayed time to bone fracture, and increased the use of the tumor-bearing limb. Consistent with animal studies in osteoarthritis and head and neck cancer, early blockade of NGF reduced weight loss in mice with bone sarcoma. In terms of the extent and time course of pain relief, NGF blockade also reduced pain 40% to 70%, depending on the metric assessed. Importantly, this analgesic effect was maintained even in animals with late-stage disease. Our results suggest that NGF blockade immediately upon detection of tumor metastasis to bone may help preserve the integrity and use, delay the time to tumor-induced bone fracture, and maintain body weight.

Indexed as

AnimalsAntibodiesBone NeoplasmsCell Line, TumorDisease Models, AnimalExtremitiesHead and Neck NeoplasmsMaleMiceMice, Inbred C3HNeoplasm MetastasisNerve Growth FactorNerve Growth FactorsOsteoarthritisPainRandom AllocationAntibodiesNerve Growth FactorNerve Growth Factors

Identifiers

PMID25287160
PMCPMC4253026
OpenAlexW2038786746

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.