Evidence map›Paper›PMID 38193115›Full record

ArticleBioengineering & translational medicine2024

An engineered niche delineates metastatic potential of breast cancer.

Sophia M Orbach, Christian Y DeVaull, Elizabeth J Bealer, Brian C Ross, Jacqueline S Jeruss, Lonnie D Shea

Open access · goldAbstract read
In one paragraph

Article in Bioengineering & translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Engineered immunological niche directs therapeutic development in models of progressive multiple sclerosis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. An engineered niche delineates metastatic potential of breast cancer.Bioengineering & translational medicine · 2024
    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

6 authors at 1 institution in 1 country.

Sophia M OrbachDepartment of Biomedical Engineering University of Michigan Ann Arbor Michigan USA.
Christian Y DeVaullDepartment of Biomedical Engineering University of Michigan Ann Arbor Michigan USA.
Elizabeth J BealerDepartment of Biomedical Engineering University of Michigan Ann Arbor Michigan USA.
Brian C RossDepartment of Biomedical Engineering University of Michigan Ann Arbor Michigan USA.
Jacqueline S JerussDepartment of Biomedical Engineering University of Michigan Ann Arbor Michigan USA.
Lonnie D SheaDepartment of Biomedical Engineering University of Michigan Ann Arbor Michigan USA.ORCID https://orcid.org/0000-0002-9296-9673
University of Michigan · US

Funding

Identifying intercellular circuits driving cell phenotypes within a nicheR01CA243916 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JERUSS, JACQUELINE SARA, SHEA, LONNIE D · 2019 to 2023
$2.3M
Measuring Signaling Pathway Dynamics During Tissue Growth in HydrogelsR01CA214384 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JERUSS, JACQUELINE SARA, SHEA, LONNIE D · 2017 to 2021
$1.8M
Tissue engineering tools for monitoring the cellular and molecular response to therapyR01CA272940 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JACQUELINE SARA JERUSS, Lonnie D Shea · 2023 to 2026
$1.7M
Heterogeneity of the Early Metastatic Niche in Cancer Progression and ChemoresistanceF32CA243421 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ORBACH, SOPHIA M · 2019 to 2021
$194k
NCI NIH HHS F32 CA243421NCI NIH HHS R01 CA214384NCI NIH HHS R01 CA243916NCI NIH HHS R01 CA272940
6 · The paper itself

Abstract

Metastatic breast cancer is often not diagnosed until secondary tumors have become macroscopically visible and millions of tumor cells have invaded distant tissues. Yet, metastasis is initiated by a cascade of events leading to formation of the pre-metastatic niche, which can precede tumor formation by a matter of years. We aimed to distinguish the potential for metastatic disease from nonmetastatic disease at early times in triple-negative breast cancer using sister cell lines 4T1 (metastatic), 4T07 (invasive, nonmetastatic), and 67NR (nonmetastatic). We used a porous, polycaprolactone scaffold, that serves as an engineered metastatic niche, to identify metastatic disease through the characteristics of the microenvironment. Analysis of the immune cell composition at the scaffold was able to distinguish noninvasive 67NR tumor-bearing mice from 4T07 and 4T1 tumor-bearing mice but could not delineate metastatic potential between the two invasive cell lines. Gene expression in the scaffolds correlated with the up-regulation of cancer hallmarks (e.g., angiogenesis, hypoxia) in the 4T1 mice relative to 4T07 mice. We developed a 9-gene signature (

Indexed as

breast cancerearly detectionengineered diagnosticsgene signature

Identifiers

PMID38193115
PMCPMC10771563
OpenAlexW4387221430

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.