<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sabei FY</submitter><funding>NCATS NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>102446</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8464505</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>37</volume><pubmed_abstract>Ewing's sarcoma (EwS) is the second most common bone cancer in children and adolescents. Current chemotherapy regimens are mainly ineffective in patients with relapsed disease and cause long-term effects in survivors. Therefore, we have developed a combinatorial therapy based on a novel drug candidate named ML111 that exhibits selective activity against EwS cells and synergizes with vincristine. To increase the aqueous solubility of hydrophobic ML111, polymeric nanoparticles (ML111-NP) were developed. In vitro data revealed that ML111-NP compromise viability of EwS cells without affecting non-malignant cells. Furthermore, ML111-NP exhibit strong synergistic effects in a combination with vincristine on EwS cells, while this drug pair exhibits antagonistic effects towards normal cells. Final</pubmed_abstract><journal>Nanomedicine : nanotechnology, biology, and medicine</journal><pubmed_title>A targeted combinatorial therapy for Ewing's sarcoma.</pubmed_title><pmcid>PMC8464505</pmcid><funding_grant_id>R37 CA234006</funding_grant_id><funding_grant_id>KL2 TR002370</funding_grant_id><funding_grant_id>R01 CA237569</funding_grant_id><pubmed_authors>Davare MA</pubmed_authors><pubmed_authors>Leid M</pubmed_authors><pubmed_authors>Esfandiari Nazzaro E</pubmed_authors><pubmed_authors>Sabei FY</pubmed_authors><pubmed_authors>Park Y</pubmed_authors><pubmed_authors>Vogel WK</pubmed_authors><pubmed_authors>Al-Fatease AM</pubmed_authors><pubmed_authors>Demessie AA</pubmed_authors><pubmed_authors>Alani A</pubmed_authors><pubmed_authors>Albarqi HA</pubmed_authors><pubmed_authors>Moses AS</pubmed_authors><pubmed_authors>Taratula O</pubmed_authors></additional><is_claimable>false</is_claimable><name>A targeted combinatorial therapy for Ewing's sarcoma.</name><description>Ewing's sarcoma (EwS) is the second most common bone cancer in children and adolescents. Current chemotherapy regimens are mainly ineffective in patients with relapsed disease and cause long-term effects in survivors. Therefore, we have developed a combinatorial therapy based on a novel drug candidate named ML111 that exhibits selective activity against EwS cells and synergizes with vincristine. To increase the aqueous solubility of hydrophobic ML111, polymeric nanoparticles (ML111-NP) were developed. In vitro data revealed that ML111-NP compromise viability of EwS cells without affecting non-malignant cells. Furthermore, ML111-NP exhibit strong synergistic effects in a combination with vincristine on EwS cells, while this drug pair exhibits antagonistic effects towards normal cells. Final</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2026-05-31T15:56:29.08Z</modification><creation>2025-04-04T12:46:28.578Z</creation></dates><accession>S-EPMC8464505</accession><cross_references><pubmed>34303840</pubmed><doi>10.1016/j.nano.2021.102446</doi></cross_references></HashMap>