Datasets describing hydrogel properties and cellular metrics for modeling of tumor dormancy

Breast cancer dormancy is an underlying challenge toward targeting and controlling metastatic recurrence and disease progression. Development of engineered, well-defined in vitro models is necessary to systematically recapitulate tumor dormancy and investigate potential therapeutic strategies. Towar...

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Main Authors: Shantanu Pradhan, John H. Slater
Format: Article
Language:English
Published: Elsevier 2019-08-01
Series:Data in Brief
Online Access:http://www.sciencedirect.com/science/article/pii/S2352340919304822
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spelling doaj-0074ab36feaa4c3f86226322c95eefd82020-11-25T02:44:09ZengElsevierData in Brief2352-34092019-08-0125Datasets describing hydrogel properties and cellular metrics for modeling of tumor dormancyShantanu Pradhan0John H. Slater1Department of Biomedical Engineering, University of Delaware, USACorresponding author.; Department of Biomedical Engineering, University of Delaware, USABreast cancer dormancy is an underlying challenge toward targeting and controlling metastatic recurrence and disease progression. Development of engineered, well-defined in vitro models is necessary to systematically recapitulate tumor dormancy and investigate potential therapeutic strategies. Toward this end, a set of sixteen hydrogel formulations with varying degrees of adhesivity and crosslink density was developed for encapsulation, three-dimensional (3D) culture, and phenotypic assessment of MDA-MB-231 breast cancer cells. The hydrogel adhesivity was regulated by incorporation of RGDS peptide conjugated to acrylate poly(ethylene glycol) (PEG-RGDS) and the crosslink density by incorporation of N-vinyl pyrrolidinone (NVP). Here, we present data concerning the characterization of hydrogel properties (PEG-RGDS incorporation, hydrogel crosslink density, and hydrogel diffusivity as a function of NVP concentration) and phenotypic metrics (viability, early apoptosis, proliferation, metabolic activity, viable cell density, and morphological features) of encapsulated MDA-MB-231s over 15 days in culture. Interpretation of this data can be found in a research article titled “Tunable Hydrogels for Controlling Phenotypic Cancer Cell States to Model Breast Cancer Dormancy and Reactivation” (Pradhan et al., 2019) [1]. Keywords: Cancer, Dormancy, Metastasis, Relapse, Hydrogel, Tissue engineeringhttp://www.sciencedirect.com/science/article/pii/S2352340919304822
collection DOAJ
language English
format Article
sources DOAJ
author Shantanu Pradhan
John H. Slater
spellingShingle Shantanu Pradhan
John H. Slater
Datasets describing hydrogel properties and cellular metrics for modeling of tumor dormancy
Data in Brief
author_facet Shantanu Pradhan
John H. Slater
author_sort Shantanu Pradhan
title Datasets describing hydrogel properties and cellular metrics for modeling of tumor dormancy
title_short Datasets describing hydrogel properties and cellular metrics for modeling of tumor dormancy
title_full Datasets describing hydrogel properties and cellular metrics for modeling of tumor dormancy
title_fullStr Datasets describing hydrogel properties and cellular metrics for modeling of tumor dormancy
title_full_unstemmed Datasets describing hydrogel properties and cellular metrics for modeling of tumor dormancy
title_sort datasets describing hydrogel properties and cellular metrics for modeling of tumor dormancy
publisher Elsevier
series Data in Brief
issn 2352-3409
publishDate 2019-08-01
description Breast cancer dormancy is an underlying challenge toward targeting and controlling metastatic recurrence and disease progression. Development of engineered, well-defined in vitro models is necessary to systematically recapitulate tumor dormancy and investigate potential therapeutic strategies. Toward this end, a set of sixteen hydrogel formulations with varying degrees of adhesivity and crosslink density was developed for encapsulation, three-dimensional (3D) culture, and phenotypic assessment of MDA-MB-231 breast cancer cells. The hydrogel adhesivity was regulated by incorporation of RGDS peptide conjugated to acrylate poly(ethylene glycol) (PEG-RGDS) and the crosslink density by incorporation of N-vinyl pyrrolidinone (NVP). Here, we present data concerning the characterization of hydrogel properties (PEG-RGDS incorporation, hydrogel crosslink density, and hydrogel diffusivity as a function of NVP concentration) and phenotypic metrics (viability, early apoptosis, proliferation, metabolic activity, viable cell density, and morphological features) of encapsulated MDA-MB-231s over 15 days in culture. Interpretation of this data can be found in a research article titled “Tunable Hydrogels for Controlling Phenotypic Cancer Cell States to Model Breast Cancer Dormancy and Reactivation” (Pradhan et al., 2019) [1]. Keywords: Cancer, Dormancy, Metastasis, Relapse, Hydrogel, Tissue engineering
url http://www.sciencedirect.com/science/article/pii/S2352340919304822
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