Evidence map›Paper›PMID 24367205›Full record

ReviewBreast cancer (Dove Medical Press)2012

Dormancy in breast cancer.

Malgorzata Banys, Andreas D Hartkopf, Natalia Krawczyk, Tatjana Kaiser, Franziska Meier-Stiegen, Tanja Fehm, Hans Neubauer

Open access · goldAbstract readReview
In one paragraph

Review in Breast cancer (Dove Medical Press), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

32 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  18. Tumor dormancy in bone.Cancer reports (Hoboken, N.J.) · 2020
    Review
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  20. Article
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 2 institutions in 1 country.

Malgorzata BanysDepartment of Obstetrics and Gynecology, University of Tuebingen, Tuebingen, Germany ; Department of Obstetrics and Gynecology, Marienkrankenhaus Hamburg, Hamburg, Germany.
Andreas D HartkopfDepartment of Obstetrics and Gynecology, University of Tuebingen, Tuebingen, Germany.
Natalia KrawczykDepartment of Obstetrics and Gynecology, University of Tuebingen, Tuebingen, Germany.
Tatjana KaiserDepartment of Obstetrics and Gynecology, University of Tuebingen, Tuebingen, Germany.
Franziska Meier-StiegenDepartment of Obstetrics and Gynecology, University of Tuebingen, Tuebingen, Germany.
Tanja FehmDepartment of Obstetrics and Gynecology, University of Tuebingen, Tuebingen, Germany.
Hans NeubauerDepartment of Obstetrics and Gynecology, University of Tuebingen, Tuebingen, Germany.
University of Tübingen · DEMarienkrankenhaus Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor dormancy describes a prolonged quiescent state in which tumor cells are present, but disease progression is not yet clinically apparent. Breast cancer is especially known for long asymptomatic periods, up to 25 years, with no evidence of the disease, followed by a relapse. Factors that determine the cell's decision to enter a dormant state and that control its duration remain unclear. In recent years, considerable progress has been made in understanding how tumor cells circulating in the blood interact and extravasate into secondary sites and which factors might determine whether these cells survive, remain dormant, or become macrometastases. The mechanisms of tumor cell dormancy are still not clear. Two different hypotheses are currently discussed: tumor cells persist either by completely withdrawing from the cell cycle or by continuing to proliferate at a slow rate that is counterbalanced by cell death. Because dormant disseminated tumor cells may be the founders of metastasis, one hypothesis is that dormant tumor cells, or at least a fraction of them, share stem cell-like characteristics that may be responsible for their long half-lives and their suggested resistance to standard chemotherapy. Therefore, knowledge of the biology of tumor cell dormancy may be the basis from which to develop innovative targeted therapies to control or eliminate this tumor cell fraction. In this review, we discuss biological mechanisms and clinical implications of tumor dormancy in breast cancer patients.

Indexed as

circulating tumor celldisseminated tumor celltargeted therapytumor dormancy

Identifiers

PMID24367205
PMCPMC3846810
OpenAlexW274400255

What OpenQuestion holds

Textmetadata
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.