Evidence map›Paper›PMID 38457510›Full record

ReviewScience advances2024

Outlook and opportunities for engineered environments of breast cancer dormancy.

Nathan R Richbourg, Ninette Irakoze, Hyuna Kim, Shelly R Peyton

Open access · goldAbstract readReview
In one paragraph

Review in Science advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.2field-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

15 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Breast cancer: pathogenesis and treatments.Signal transduction and targeted therapy · 2025
    Review
  12. Review
  13. Article
  14. Multi-stage mechanisms of tumor metastasis and therapeutic strategies.Signal transduction and targeted therapy · 2024
    Review
  15. 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

4 authors at 2 institutions in 1 country.

Nathan R RichbourgDepartment of Chemical Engineering, University of Massachusetts Amherst, MA 01003, USA.ORCID 0000-0002-5091-3321
Ninette IrakozeDepartment of Chemical Engineering, University of Massachusetts Amherst, MA 01003, USA.
Hyuna KimMolecular and Cellular Biology Graduate Program, University of Massachusetts Amherst, MA 01003, USA.ORCID 0000-0001-6954-6595
Shelly R PeytonDepartment of Chemical Engineering, University of Massachusetts Amherst, MA 01003, USA.ORCID 0000-0002-7364-8727
University of Massachusetts Amherst · USAmherst College · US

Funding

CHEMISTRY-BIOLOGY INTERFACE PREDOCTORAL TRAINING GRANTST32GM008515 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI THOMPSON, LYNMARIE K. · 1995 to 2020
$4.3M
Biotechnology Training Program in Applied Life SciencesT32GM135096 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI Jeanne Ann Hardy, Ashish A. Kulkarni · 2020 to 2026
$3.9M
Chemistry-Biology Interface Predoctoral Training GrantT32GM139789 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI ERIC Robert STRIETER · 2021 to 2026
$3.4M
Personalization and Failure Testing of Dual Switch Gene Drives in Lung CancerU01CA265709 · NCI · PENNSYLVANIA STATE UNIVERSITY, THE · PI PRITCHARD, JUSTIN · 2021 to 2025
$2.6M
NCI NIH HHS U01 CA265709NIGMS NIH HHS T32 GM008515NIGMS NIH HHS T32 GM135096NIGMS NIH HHS T32 GM139789
6 · The paper itself

Abstract

Dormant, disseminated breast cancer cells resist treatment and may relapse into malignant metastases after decades of quiescence. Identifying how and why these dormant breast cancer cells are triggered into outgrowth is a key unsolved step in treating latent, metastatic breast cancer. However, our understanding of breast cancer dormancy in vivo is limited by technical challenges and ethical concerns with triggering the activation of dormant breast cancer. In vitro models avoid many of these challenges by simulating breast cancer dormancy and activation in well-controlled, bench-top conditions, creating opportunities for fundamental insights into breast cancer biology that complement what can be achieved through animal and clinical studies. In this review, we address clinical and preclinical approaches to treating breast cancer dormancy, how precisely controlled artificial environments reveal key interactions that regulate breast cancer dormancy, and how future generations of biomaterials could answer further questions about breast cancer dormancy.

Indexed as

Neoplasm Recurrence, LocalAnimalsCell Division

Identifiers

PMID38457510
PMCPMC10923521
OpenAlexW4392581188

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.