Evidence map›Paper›PMID 39628034›Full record

ArticleBiotechnology and bioengineering2025

Design Principles of an Engineered Metastatic Niche for Monitoring of Cancer Progression.

Guillermo Escalona, Ramon Ocadiz-Ruiz, Jeffrey A Ma, Ian A Schrack, Brian C Ross, Alexis K Morrison, Jacqueline S Jeruss, Lonnie D Shea

Abstract read
In one paragraph

Article in Biotechnology and bioengineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Guillermo EscalonaDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0009-0009-4756-5424
Ramon Ocadiz-RuizDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Jeffrey A MaDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Ian A SchrackDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Brian C RossDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
Alexis K MorrisonDepartment 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 0000-0002-9296-9673

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
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
NCI NIH HHS R01 CA243916NCI NIH HHS R01 CA272940This work was supported by the National Cancer Institute (grants R01CA272940 and R01CA243916).
6 · The paper itself

Abstract

Across many types of cancer, metastatic disease is associated with a substantial decrease in 5-year survival rates relative to only a localized primary tumor. Many patients self-report metastatic disease due to disruption of normal organ or tissue function, and earlier detection could enable treatment with a lower burden of disease. We have previously reported a subcutaneous biomaterial implant for early detection by serving as an engineered metastatic niche, which has been reported to recruit tumor cells before colonization of solid organs. In this report, we investigated the design principles of the scaffold and defined the conditions for use in disease detection. Using the metastatic 4T1 triple-negative breast cancer model, we identified that a porous structure was essential to capture tumor and immune cells. Scaffolds of multiple diameters were investigated for their ability to serve as a metastatic niche, with a porous scaffold with a diameter as small as 2 mm identifying disease accurately. Additionally, scaffolds that had been in vivo for 1-5 weeks were able to identify disease accurately. Finally, the sensitivity of the scaffold relative to liquid biopsies was analyzed, with scaffolds accurately detecting disease at earlier time points than liquid biopsy. Collectively, these studies inform the design principles and use conditions for porous scaffolds to detect metastatic disease.

Indexed as

Neoplasm MetastasisTissue ScaffoldsAnimalsCell Line, TumorDisease ProgressionFemaleHumansMicebiomaterialsbreast cancerdiagnostic technologiesearly detectionmetastatsistissue engineering

Identifiers

PMID39628034
PMCPMC11808458

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Registered trials

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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.