Evidence map›Paper›PMID 33689396›Full record

ArticleMolecular biology of the cell2021

The effect of marrow secretome and culture environment on the rate of metastatic breast cancer cell migration in two and three dimensions.

Kimberly J Curtis, Christine Mai, Hannah Martin, Alyssa G Oberman, Laura Alderfer, Ricardo Romero-Moreno, Mark Walsh, Stephen F Mitros, Scott G Thomas, Joseph A Dynako and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology of the cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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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

14 authors at 4 institutions in 2 countries.

Kimberly J CurtisBioengineering Graduate Program, University of Notre Dame, IN 46556.
Christine MaiDepartment of Aerospace and Mechanical Engineering, University of Notre Dame, IN 46556.
Hannah MartinDepartment of Aerospace and Mechanical Engineering, University of Notre Dame, IN 46556.
Alyssa G ObermanBioengineering Graduate Program, University of Notre Dame, IN 46556.
Laura AlderferBioengineering Graduate Program, University of Notre Dame, IN 46556.
Ricardo Romero-MorenoDepartment of Chemistry and Biochemistry, University of Notre Dame, IN 46556.
Mark WalshIndiana University School of Medicine, South Bend Campus, Notre Dame, IN 46556.
Stephen F MitrosBeacon Medical Group, Trauma and Surgical Services, South Bend, IN, 46601.
Scott G ThomasIndiana University School of Medicine, South Bend Campus, Notre Dame, IN 46556.
Joseph A DynakoIndiana University School of Medicine, South Bend Campus, Notre Dame, IN 46556.
David I ZimmerIndiana University School of Medicine, South Bend Campus, Notre Dame, IN 46556.
Laoise M McNamaraMechanobiology and Medical Devices Research Group, Biomedical Engineering, College of Engineering and Informatics, National University of Ireland, Galway, Ireland H91 CF50.
Laurie E LittlepageDepartment of Chemistry and Biochemistry, University of Notre Dame, IN 46556.
Glen L NieburBioengineering Graduate Program, University of Notre Dame, IN 46556.
University of Notre Dame · USIndiana University School of MedicineBeacon Health System · USOllscoil na Gaillimhe – University of Galway · IE

Funding

NRSA Training CoreTL1TR002531 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI FOTI, DANIEL JUSTIN, HURLEY, THOMAS D. · 2018 to 2022
$2.5M
Online Raman Diagnostics of OncometabolitesR33CA206922 · NCI · UNIVERSITY OF NOTRE DAME · PI SCHULTZ, ZACHARY · 2016 to 2018
$1.0M
NCATS NIH HHS TL1 TR002531NCI NIH HHS R33 CA206922
6 · The paper itself

Abstract

Metastasis is responsible for over 90% of cancer-related deaths, and bone is the most common site for breast cancer metastasis. Metastatic breast cancer cells home to trabecular bone, which contains hematopoietic and stromal lineage cells in the marrow. As such, it is crucial to understand whether bone or marrow cells enhance breast cancer cell migration toward the tissue. To this end, we quantified the migration of MDA-MB-231 cells toward human bone in two- and three-dimensional (3D) environments. First, we found that the cancer cells cultured on tissue culture plastic migrated toward intact trabecular bone explants at a higher rate than toward marrow-deficient bone or devitalized bone. Leptin was more abundant in conditioned media from the cocultures with intact explants, while higher levels of IL-1β, IL-6, and TNFα were detected in cultures with both intact bone and cancer cells. We further verified that the cancer cells migrated into bone marrow using a bioreactor culture system. Finally, we studied migration toward bone in 3D gelatin. Migration speed did not depend on stiffness of this homogeneous gel, but many more dendritic-shaped cancer cells oriented and migrated toward bone in stiffer gels than softer gels, suggesting a coupling between matrix mechanics and chemotactic signals.

Indexed as

Cell MovementBioreactorsBone MarrowBone NeoplasmsBreast NeoplasmsCell Culture TechniquesChemokinesChemotactic FactorsCulture Media, ConditionedCytokinesHydrogelsNeoplasm MetastasisNeoplastic Cells, CirculatingTumor Cells, CulturedChemokinesChemotactic FactorsCulture Media, ConditionedCytokinesHydrogels

Identifiers

PMID33689396
PMCPMC8101488
OpenAlexW3135815753

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.