Evidence map›Paper›PMID 25681658›Full record

ReviewPharmacology & therapeutics2015

HIF targets in bone remodeling and metastatic disease.

Rachelle W Johnson, Ernestina Schipani, Amato J Giaccia

Abstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Mechanisms of breast cancer dormancy in bone metastasis.Clinical & experimental metastasis · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Tumor dormancy in bone.Cancer reports (Hoboken, N.J.) · 2020
    Review
  18. Breast Cancer Dormancy in Bone.Current osteoporosis reports · 2019
    Review
  19. Article
  20. 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

3 authors at 2 institutions in 1 country.

Rachelle W JohnsonDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA, United States.
Ernestina SchipaniDepartment of Orthopaedic Surgery, Medical School, University of Michigan, Ann Arbor, MI, United States; Department of Medicine and Endocrinology, Medical School, University of Michigan, Ann Arbor, MI, United States.
Amato J GiacciaDepartment of Radiation Oncology, Stanford University School of Medicine, Stanford, CA, United States. Electronic address: giaccia@stanford.edu.
Stanford University · USUniversity of Michigan–Ann Arbor · US

Funding

HIF-1alpha, a Survival and Differentiation Factor for CartilageR01AR065403 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCHIPANI, ERNESTINA · 2013 to 2017
$1.7M
NIAMS NIH HHS R01 AR065403
6 · The paper itself

Abstract

The bone marrow is a hypoxic microenvironment that is rich in growth factors and blood vessels and is readily colonized by tumor cells disseminated from numerous cancers including tumors of the breast, prostate, lung, and skin. The origin of metastatic growth promoting factors for tumor cells disseminated to the bone marrow is derived from multiple sources: the bone matrix, which is a reservoir for growth factors, and cells residing in the marrow and along bone surfaces, such as osteoblasts, osteoclasts, macrophages, and T cells, which secrete cytokines and chemokines. Low oxygen levels within the bone marrow induce hypoxia signaling pathways such as hypoxia inducible factor (HIF), which is regulated by oxygen requiring prolyl hydroxylases (PHDs) and von Hippel-Lindau (VHL) tumor suppressor. These hypoxia signaling pathways have profound effects on bone development and homeostasis. Likewise, hypoxic conditions observed in local breast and prostate tumors point to a role for hypoxia-inducible genes in metastasis to and colonization of the bone marrow. This review will explore the role of hypoxia-regulated factors in bone development and remodeling, and how these elements may contribute to solid tumor metastasis to the bone.

Indexed as

Bone RemodelingAntineoplastic AgentsBone DevelopmentBone NeoplasmsCell HypoxiaHumansHypoxia-Inducible Factor 1Molecular Targeted TherapyProlyl HydroxylasesTumor MicroenvironmentVon Hippel-Lindau Tumor Suppressor ProteinAntineoplastic AgentsHypoxia-Inducible Factor 1Prolyl HydroxylasesVon Hippel-Lindau Tumor Suppressor ProteinBone metastasisBone microenvironmentHIFHypoxiaPHDRemodeling

Identifiers

PMID25681658
PMCPMC4414805
OpenAlexW2024817199

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.