Evidence map›Paper›PMID 26716792›Full record

ArticleBiofabrication2015

A simple engineered platform reveals different modes of tumor-microenvironmental cell interaction.

Chentian Zhang, Elizabeth M Shenk, Laura C Blaha, Byungwoo Ryu, Rhoda M Alani, Mario Cabodi, Joyce Y Wong

Open access · greenAbstract read
In one paragraph

Article in Biofabrication, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 1 institution in 1 country.

Chentian ZhangDepartment of Biomedical Engineering, Boston University, Boston, MA, 02215, USA.
Elizabeth M ShenkDepartment of Biomedical Engineering, Boston University, Boston, MA, 02215, USA.
Laura C BlahaDepartment of Biomedical Engineering, Boston University, Boston, MA, 02215, USA.
Byungwoo RyuDepartment of Dermatology, Boston University School of Medicine, Boston, MA, 02118, USA.
Rhoda M AlaniDepartment of Dermatology, Boston University School of Medicine, Boston, MA, 02118, USA.
Mario CabodiDepartment of Biomedical Engineering, Boston University, Boston, MA, 02215, USA.
Joyce Y WongDepartment of Biomedical Engineering, Boston University, Boston, MA, 02215, USA.
Boston University · US

Funding

Center for Innovation in Point of Care Technologies for the Future of Cancer CareU54EB015403 · NIBIB · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI KLAPPERICH, CATHERINE M. · 2012 to 2016
$8.9M
TRAINING IN BIOMOLECULAR PHARMACOLOGYT32GM008541 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FARB, DAVID H · 1997 to 2022
$5.2M
Boston University Cross-Disciplinary Training in Nanotechnology for CancerR25CA153955 · NCI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI FALLER, DOUGLAS V, GOLDBERG, BENNETT B · 2010 to 2014
$2.1M
NCI NIH HHS R25 CA153955NCI NIH HHS R25CA153955NIBIB NIH HHS U54 EB015403NIGMS NIH HHS 5T32GM008541-17NIGMS NIH HHS T32 GM008541
6 · The paper itself

Abstract

How metastatic cancer lesions survive and grow in secondary locations is not fully understood. There is a growing appreciation for the importance of tumor components, i.e. microenvironmental cells, in this process. Here, we used a simple microfabricated dual cell culture platform with a 500 μm gap to assess interactions between two different metastatic melanoma cell lines (1205Lu isolated from a lung lesion established through a mouse xenograft; and WM852 derived from a stage III metastatic lesion of skin) and microenvironmental cells derived from either skin (fibroblasts), lung (epithelial cells) or liver (hepatocytes). We observed differential bi-directional migration between microenvironmental cells and melanoma, depending on the melanoma cell line. Lung epithelial cells and skin fibroblasts, but not hepatocytes, stimulated higher 1205Lu migration than without microenvironmental cells; in the opposite direction, 1205Lu cells induced hepatocytes to migrate, but had no effect on skin fibroblasts and slightly inhibited lung epithelial cells. In contrast, none of the microenvironments had a significant effect on WM852; in this case, skin fibroblasts and hepatocytes--but not lung epithelial cells--exhibited directed migration toward WM852. These observations reveal significant effects a given microenvironmental cell line has on the two different melanoma lines, as well as how melanoma effects different microenvironmental cell lines. Our simple platform thus has potential to provide complex insights into different strategies used by cancerous cells to survive in and colonize metastatic sites.

Indexed as

Cell CommunicationAnimalsCell Line, TumorCoculture TechniquesEquipment DesignEquipment Failure AnalysisLab-On-A-Chip DevicesMelanomaMicePrinting, Three-DimensionalTissue EngineeringTumor MicroenvironmentViscera

Identifiers

PMID26716792
PMCPMC4854650
OpenAlexW2206622299

What OpenQuestion holds

Textmetadata
LicenceTDM
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.