Evidence map›Paper›PMID 31468498›Full record

ReviewCurrent osteoporosis reports2019

Breast Cancer Dormancy in Bone.

Miranda E Clements, Rachelle W Johnson

Abstract readReview
In one paragraph

Review in Current osteoporosis reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
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

23 citing papers in PubMed.

  1. Review
  2. Mechanisms of breast cancer dormancy in bone metastasis.Clinical & experimental metastasis · 2026
    Review
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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

2 authors.

Miranda E ClementsVanderbilt Center for Bone Biology, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
Rachelle W JohnsonVanderbilt Center for Bone Biology, Vanderbilt University Medical Center, Nashville, TN, 37232, USA. rachelle.johnson@vumc.org.

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

purpose of reviewThe goal of this review is to summarize recent experimental and clinical evidence for metastatic latency and the molecular mechanisms that regulate tumor dormancy in the bone. RECENT

findingsTumor dormancy contributes to the progression of metastasis and thus has significant clinical implications for prognosis and treatment. Tumor-intrinsic signaling and specialized bone marrow niches play a pivotal role in determining the dormancy status of bone disseminated tumor cells. Experimental models have provided significant insight into the effects of the bone microenvironment on tumor cells; however, these models remain limited in their ability to study dormancy. Despite recent advances in the mechanistic understanding of how tumor cells remain dormant in the bone for prolonged periods of time, the signals that trigger spontaneous dormancy escape remain unclear. This review highlights the need for further investigation of mechanisms underlying tumor dormancy using clinically relevant models.

Indexed as

Tumor MicroenvironmentAnimalsBone MarrowBone NeoplasmsBreast NeoplasmsDisease Models, AnimalDisease ProgressionFemaleHumansMiceNeoplasm MetastasisSignal TransductionBone metastasisBreast cancerTumor dormancy

Identifiers

PMID31468498
PMCPMC6819229

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.