<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bersini S</submitter><funding>NCI NIH HHS</funding><pagination>36110-36125</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6281425</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(90)</volume><pubmed_abstract>The reciprocal interaction between circulating tumor cells (CTCs) and tissue-specific cells is influential for the progression of metastases. In particular, the process of extravasation relies on the complex cross-talk between cancer cells and other cellular players such as the endothelium and the secondary tissue. However, most &lt;i>in vitro&lt;/i> studies only focus on one heterotypic cell-cell interaction and often lack of physiological relevance. In this project, we investigated both CTC-endothelium and CTC-secondary site interactions during cancer cell extravasation. We first used a microarray analysis of extravasated MDA-MB-231 breast cancer cells to identify key markers involved in extravasation. Then, we developed a tri-culture microfluidic platform combining cancer cells, endothelium a</pubmed_abstract><journal>Oncotarget</journal><pubmed_title>A combined microfluidic-transcriptomic approach to characterize the extravasation potential of cancer cells.</pubmed_title><pmcid>PMC6281425</pmcid><funding_grant_id>U01 CA202177</funding_grant_id><pubmed_authors>Moretti M</pubmed_authors><pubmed_authors>Miermont A</pubmed_authors><pubmed_authors>Kamm RD</pubmed_authors><pubmed_authors>Bersini S</pubmed_authors><pubmed_authors>Adriani G</pubmed_authors><pubmed_authors>Thiery JP</pubmed_authors><pubmed_authors>Pavesi A</pubmed_authors></additional><is_claimable>false</is_claimable><name>A combined microfluidic-transcriptomic approach to characterize the extravasation potential of cancer cells.</name><description>The reciprocal interaction between circulating tumor cells (CTCs) and tissue-specific cells is influential for the progression of metastases. In particular, the process of extravasation relies on the complex cross-talk between cancer cells and other cellular players such as the endothelium and the secondary tissue. However, most &lt;i>in vitro&lt;/i> studies only focus on one heterotypic cell-cell interaction and often lack of physiological relevance. In this project, we investigated both CTC-endothelium and CTC-secondary site interactions during cancer cell extravasation. We first used a microarray analysis of extravasated MDA-MB-231 breast cancer cells to identify key markers involved in extravasation. Then, we developed a tri-culture microfluidic platform combining cancer cells, endothelium a</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Nov</publication><modification>2026-05-06T06:27:42.492Z</modification><creation>2019-10-30T08:14:29Z</creation></dates><accession>S-EPMC6281425</accession><cross_references><pubmed>30546831</pubmed><doi>10.18632/oncotarget.26306</doi></cross_references></HashMap>