Evidence map›Paper›PMID 30918918›Full record

ReviewJBMR plus2019

Bone as a Preferential Site for Metastasis.

Miranda E Sowder, Rachelle W Johnson

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in JBMR plus, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04167605 (Evaluation of Prognostic Factors), which is not on this map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.5field-weighted citation impact, top 8% 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.

NCT04167605 unknown statusnot on this mapstarted 2020, after this paper: background citation

Evaluation of Prognostic Factors: From Breast Cancer to Bone Metastases

TypeobservationalSponsorI.R.C.C.S Ospedale Galeazzi-Sant'AmbrogioRan2020 to 2024Enrolled30ConditionsBreast Cancer Metastatic, Bone MetastasesArmsBone metastasis, Breast cancer metastatic to bone
3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 68 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Evaluating the Efficacy of Polyphenol-Enriched Plant Extracts and Pathway Modulators in the Bone Marrow to Suppress Breast Cancer Progression.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Epigenetic control of the vicious cycle.Journal of bone oncology · 2024
    Article
  18. Review
  19. Nanoparticle-mediated synergistic drug combination for treating bone metastasis.Journal of controlled release : official journal of the Controlled Release Society · 2023
    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

2 authors at 2 institutions in 1 country.

Miranda E SowderProgram in Cancer Biology Vanderbilt University Nashville TN USA.
Rachelle W JohnsonProgram in Cancer Biology Vanderbilt University Nashville TN USA.
Vanderbilt University · USVanderbilt University Medical Center · US

Funding

CHARACTERIZATION OF BREAST CANCER DORMANCY IN BONER00CA194198 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI JOHNSON, RACHELLE W · 2016 to 2018
$747k
NCI NIH HHS R00 CA194198
6 · The paper itself

Abstract

Bone marrow provides a unique microenvironment favoring the colonization and outgrowth of metastatic tumor cells. Despite the high incidence of bone metastasis in breast and prostate cancer patients, many of the molecular mechanisms controlling metastatic progression remain unclear. Several gene signatures associated with bone metastasis have been reported, but no metastasis-specific gene alterations have been identified. Therefore, there has been considerable interest in understanding how the bone microenvironment impacts the behavior of disseminated tumor cells (DTCs) prior to and following colonization of the bone. Substantial evidence indicates that disruption of normal bone homeostasis by tumor-derived factors establishes a premetastatic niche within the bone that favors DTC colonization. Following dissemination, bone resident cells and the surrounding stroma provide critical signals that support tumor cell colonization, survival, and eventual outgrowth. Clinical data suggest that patients can harbor DTCs for years to decades prior to developing overt bone metastases, suggesting a period of tumor dormancy occurs in the bone marrow. Several dormancy-promoting factors have been recently identified; however, critical questions surrounding the molecular triggers and timing of tumor cell emergence from dormancy remain. Here, we review how metastatic tumor cells co-opt the bone marrow microenvironment for metastatic progression and discuss emerging insights into how to more effectively target DTCs and prevent metastasis. © 2018 The Authors.

Indexed as

BONE METASTASISCOLONIZATIONDORMANCYHOMINGPREMETASTATIC NICHE

Identifiers

PMID30918918
PMCPMC6419612
OpenAlexW2903503766

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.