Evidence map›Paper›PMID 36660589›Full record

ArticleCellular and molecular bioengineering2023

Adipose Cells Induce Escape from an Engineered Human Breast Microtumor Independently of their Obesity Status.

Yoseph W Dance, Mackenzie C Obenreder, Alex J Seibel, Tova Meshulam, Joshua W Ogony, Nikhil Lahiri, Laura Pacheco-Spann, Derek C Radisky, Matthew D Layne, Stephen R Farmer and 2 more

Abstract read
In one paragraph

Article in Cellular and molecular bioengineering, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Monocytes are biological sensors of aging and frailty in humans.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. 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

12 authors.

Yoseph W DanceDepartment of Biomedical Engineering, Boston University, 44 Cummington Mall, Boston, MA 02215 USA.
Mackenzie C ObenrederDepartment of Biomedical Engineering, Boston University, 44 Cummington Mall, Boston, MA 02215 USA.
Alex J SeibelDepartment of Biomedical Engineering, Boston University, 44 Cummington Mall, Boston, MA 02215 USA.
Tova MeshulamBoston Nutrition Obesity Research Center, Boston University School of Medicine, Boston, MA USA.
Joshua W OgonyDepartment of Cancer Biology, Mayo Clinic Comprehensive Cancer Center, Jacksonville, FL USA.
Nikhil LahiriDepartment of Biomedical Engineering, Boston University, 44 Cummington Mall, Boston, MA 02215 USA.
Laura Pacheco-SpannDepartment of Quantitative Health Sciences, Mayo Clinic Comprehensive Cancer Center, Jacksonville, FL USA.
Derek C RadiskyDepartment of Cancer Biology, Mayo Clinic Comprehensive Cancer Center, Jacksonville, FL USA.
Matthew D LayneDepartment of Biochemistry, Boston University School of Medicine, Boston, MA USA.
Stephen R FarmerBoston Nutrition Obesity Research Center, Boston University School of Medicine, Boston, MA USA.
Celeste M NelsonDepartment of Chemical and Biological Engineering, Princeton University, 303 Hoyt Laboratory, 25 William Street, Princeton, NJ 08544 USA.
Joe TienDepartment of Biomedical Engineering, Boston University, 44 Cummington Mall, Boston, MA 02215 USA.ORCID 0000-0003-4283-3986

Funding

Transgenic CoreP30DK046200 · NIDDK · TUFTS MEDICAL CENTER · PI HU, FRANK B · 1992 to 2021
$25.0M
Engineered Invasive Human Breast Tumors with Integrated Capillaries and LymphaticsU01CA214292 · NCI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI NELSON, CELESTE M, TIEN, JOE Y · 2017 to 2021
$3.2M
Involution-based biomarkers of breast cancer riskR01CA237602 · NCI · MAYO CLINIC JACKSONVILLE · PI DEGNIM, AMY C, RADISKY, DEREK C · 2020 to 2024
$2.8M
NCI NIH HHS R01 CA237602NCI NIH HHS U01 CA214292NIDDK NIH HHS P30 DK046200
6 · The paper itself

Abstract

Introduction: Obesity is associated with increased breast cancer incidence, recurrence, and mortality. Adipocytes and adipose-derived stem cells (ASCs), two resident cell types in adipose tissue, accelerate the early stages of breast cancer progression. It remains unclear whether obesity plays a role in the subsequent escape of malignant breast cancer cells into the local circulation. Methods: We engineered models of human breast tumors with adipose stroma that exhibited different obesity-specific alterations. We used these models to assess the invasion and escape of breast cancer cells into an empty, blind-ended cavity (as a mimic of a lymphatic vessel) for up to sixteen days. Results: Lean and obese donor-derived adipose stroma hastened escape to similar extents. Moreover, a hypertrophic adipose stroma did not affect the rate of adipose-induced escape. When admixed directly into the model tumors, lean and obese donor-derived ASCs hastened escape similarly. Conclusions: This study demonstrates that the presence of adipose cells, independently of the obesity status of the adipose tissue donor, hastens the escape of human breast cancer cells in multiple models of obesity-associated breast cancer. Supplementary Information: The online version contains supplementary material available at 10.1007/s12195-022-00750-y.

Indexed as

FatHypertrophyIntravasationMicrophysiological systemMicrovascular tissue engineeringTriple-negative breast cancerTumor engineering

Identifiers

PMID36660589
PMCPMC9842842

What OpenQuestion holds

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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.