<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Matossian MD</submitter><funding>NIBIB NIH HHS</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><pagination>127-144</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8732292</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>Metaplastic breast carcinoma (MBC) is a rare breast cancer subtype with rapid growth, high rates of metastasis, recurrence and drug resistance, and diverse molecular and histological heterogeneity. Patient-derived xenografts (PDXs) provide a translational tool and physiologically relevant system to evaluate tumor biology of rare subtypes. Here, we provide an in-depth comprehensive characterization of a new PDX model for MBC, TU-BcX-4IC. TU-BcX-4IC is a clinically aggressive tumor exhibiting rapid growth in vivo, spontaneous metastases, and elevated levels of cell-free DNA and circulating tumor cell DNA. Relative chemosensitivity of primary cells derived from TU-BcX-4IC was performed using the National Cancer Institute (NCI) oncology drug set, crystal violet staining, and cytotoxic live/dea</pubmed_abstract><journal>Clinical &amp; translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico</journal><pubmed_title>In-depth characterization of a new patient-derived xenograft model for metaplastic breast carcinoma to identify viable biologic targets and patterns of matrix evolution within rare tumor types.</pubmed_title><pmcid>PMC8732292</pmcid><funding_grant_id>R01 CA174785</funding_grant_id><funding_grant_id>T34 GM136452</funding_grant_id><funding_grant_id>T32 EB027632</funding_grant_id><funding_grant_id>1R15CA176496-01A1</funding_grant_id><funding_grant_id>R01-CA125806-04</funding_grant_id><funding_grant_id>R15 CA176496</funding_grant_id><funding_grant_id>U54 GM104940</funding_grant_id><funding_grant_id>R01 CA125806</funding_grant_id><funding_grant_id>R01-CA174785-A1</funding_grant_id><pubmed_authors>Zea AH</pubmed_authors><pubmed_authors>Brown H</pubmed_authors><pubmed_authors>Ochoa A</pubmed_authors><pubmed_authors>Elliott S</pubmed_authors><pubmed_authors>Baddoo M</pubmed_authors><pubmed_authors>Burks HE</pubmed_authors><pubmed_authors>Hebert KL</pubmed_authors><pubmed_authors>Sirenko O</pubmed_authors><pubmed_authors>Izadpanah R</pubmed_authors><pubmed_authors>Zabaleta J</pubmed_authors><pubmed_authors>Sabol RA</pubmed_authors><pubmed_authors>Martin EC</pubmed_authors><pubmed_authors>Wright MK</pubmed_authors><pubmed_authors>Windsor GO</pubmed_authors><pubmed_authors>Miele L</pubmed_authors><pubmed_authors>Moroz K</pubmed_authors><pubmed_authors>Matossian MD</pubmed_authors><pubmed_authors>King CT</pubmed_authors><pubmed_authors>Alzoubi MS</pubmed_authors><pubmed_authors>Chang T</pubmed_authors><pubmed_authors>Flemington E</pubmed_authors><pubmed_authors>Nguyen K</pubmed_authors><pubmed_authors>Bunnell BA</pubmed_authors><pubmed_authors>Riker AI</pubmed_authors><pubmed_authors>Burow ME</pubmed_authors><pubmed_authors>Sinha S</pubmed_authors><pubmed_authors>Wathieu H</pubmed_authors><pubmed_authors>Bursavich JB</pubmed_authors><pubmed_authors>Lau F</pubmed_authors><pubmed_authors>Cromwell EF</pubmed_authors><pubmed_authors>Savoie JJ</pubmed_authors><pubmed_authors>Ham AM</pubmed_authors><pubmed_authors>Collins-Burow BM</pubmed_authors></additional><is_claimable>false</is_claimable><name>In-depth characterization of a new patient-derived xenograft model for metaplastic breast carcinoma to identify viable biologic targets and patterns of matrix evolution within rare tumor types.</name><description>Metaplastic breast carcinoma (MBC) is a rare breast cancer subtype with rapid growth, high rates of metastasis, recurrence and drug resistance, and diverse molecular and histological heterogeneity. Patient-derived xenografts (PDXs) provide a translational tool and physiologically relevant system to evaluate tumor biology of rare subtypes. Here, we provide an in-depth comprehensive characterization of a new PDX model for MBC, TU-BcX-4IC. TU-BcX-4IC is a clinically aggressive tumor exhibiting rapid growth in vivo, spontaneous metastases, and elevated levels of cell-free DNA and circulating tumor cell DNA. Relative chemosensitivity of primary cells derived from TU-BcX-4IC was performed using the National Cancer Institute (NCI) oncology drug set, crystal violet staining, and cytotoxic live/dea</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2026-06-17T05:13:17.341Z</modification><creation>2022-02-11T15:22:54.749Z</creation></dates><accession>S-EPMC8732292</accession><cross_references><pubmed>34370182</pubmed><doi>10.1007/s12094-021-02677-8</doi></cross_references></HashMap>