<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(3)</volume><submitter>Shah L</submitter><funding>University of Manchester</funding><pubmed_abstract>Increased breast tissue stiffness is correlated with breast cancer risk and invasive cancer progression. However, its role in promoting bone metastasis, a major cause of mortality, is not yet understood. It is previously identified that the composition and stiffness of alginate-based hydrogels mimicking normal (1-2 kPa) and cancerous (6-10 kPa) breast tissue govern phenotype of breast cancer cells (including MDA-MB-231) in vitro. Here, to understand the causal effect of primary tumor stiffness on metastatic potential, a new breast-to-bone in vitro model is described. Together with alginate-gelatin hydrogels to mimic breast tissue, 3D printed biohybrid poly-caprolactone (PCL)-composite scaffolds, decellularized following bone-ECM deposition through Saos-2 engraftment, are used to mimic the </pubmed_abstract><journal>Advanced healthcare materials</journal><pagination>e2201898</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11468571</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Invasion and Secondary Site Colonization as a Function of In Vitro Primary Tumor Matrix Stiffness: Breast to Bone Metastasis.</pubmed_title><pmcid>PMC11468571</pmcid><pubmed_authors>Williams KJ</pubmed_authors><pubmed_authors>Shah L</pubmed_authors><pubmed_authors>Mancuso E</pubmed_authors><pubmed_authors>Latif A</pubmed_authors><pubmed_authors>Tirella A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Invasion and Secondary Site Colonization as a Function of In Vitro Primary Tumor Matrix Stiffness: Breast to Bone Metastasis.</name><description>Increased breast tissue stiffness is correlated with breast cancer risk and invasive cancer progression. However, its role in promoting bone metastasis, a major cause of mortality, is not yet understood. It is previously identified that the composition and stiffness of alginate-based hydrogels mimicking normal (1-2 kPa) and cancerous (6-10 kPa) breast tissue govern phenotype of breast cancer cells (including MDA-MB-231) in vitro. Here, to understand the causal effect of primary tumor stiffness on metastatic potential, a new breast-to-bone in vitro model is described. Together with alginate-gelatin hydrogels to mimic breast tissue, 3D printed biohybrid poly-caprolactone (PCL)-composite scaffolds, decellularized following bone-ECM deposition through Saos-2 engraftment, are used to mimic the </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-04T01:16:53.427Z</modification><creation>2025-04-04T01:16:53.427Z</creation></dates><accession>S-EPMC11468571</accession><cross_references><pubmed>36351739</pubmed><doi>10.1002/adhm.202201898</doi></cross_references></HashMap>