<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Holota M</submitter><funding>MINECO</funding><funding>Junta de Comunidades de Castilla-la Mancha</funding><funding>Polish National Agency for Academic Exchange</funding><funding>Comunidad de Madrid and University of Alcalá</funding><funding>National Science Centre, Poland</funding><funding>Ministry of Economy, Industry and Competitiveness</funding><funding>Ministry of Universities</funding><funding>National Science Center</funding><funding>Junta de Comunidades de Castilla–la Mancha</funding><funding>European Regional Development Fund</funding><pagination>4076</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9960994</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(4)</volume><pubmed_abstract>Copper carbosilane metallodendrimers containing chloride ligands and nitrate ligands were mixed with commercially available conventional anticancer drugs, doxorubicin, methotrexate and 5-fluorouracil, for a possible therapeutic system. To verify the hypothesis that copper metallodendrimers can form conjugates with anticancer drugs, their complexes were biophysically characterized using zeta potential and zeta size methods. Next, to confirm the existence of a synergetic effect of dendrimers and drugs, in vitro studies were performed. The combination therapy has been applied in two cancer cell lines: MCF-7 (human breast cancer cell line) and HepG2 (human liver carcinoma cell line). The doxorubicin (DOX), methotrexate (MTX) and 5-fluorouracil (5-FU) were more effective against cancer cells wh</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Combination of Copper Metallodendrimers with Conventional Antitumor Drugs to Combat Cancer in In Vitro Models.</pubmed_title><pmcid>PMC9960994</pmcid><funding_grant_id>2017-T2/IND-5243</funding_grant_id><funding_grant_id>CM/BG/2021-01</funding_grant_id><funding_grant_id>2018/31/F/NZ5/03454</funding_grant_id><funding_grant_id>PPN/BIL/2018/1/00150</funding_grant_id><funding_grant_id>NanoTENDO</funding_grant_id><funding_grant_id>B2017/BMD-3733</funding_grant_id><funding_grant_id>EUROPARTNER</funding_grant_id><funding_grant_id>CTQ2017-86224-P</funding_grant_id><funding_grant_id>685451</funding_grant_id><funding_grant_id>SBPLY/17/180501/000358</funding_grant_id><pubmed_authors>Bryszewska M</pubmed_authors><pubmed_authors>Garcia-Gallego S</pubmed_authors><pubmed_authors>Holota M</pubmed_authors><pubmed_authors>Michlewska S</pubmed_authors><pubmed_authors>de la Mata FJ</pubmed_authors><pubmed_authors>Del Olmo NS</pubmed_authors><pubmed_authors>Ortega P</pubmed_authors><pubmed_authors>Ionov M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Combination of Copper Metallodendrimers with Conventional Antitumor Drugs to Combat Cancer in In Vitro Models.</name><description>Copper carbosilane metallodendrimers containing chloride ligands and nitrate ligands were mixed with commercially available conventional anticancer drugs, doxorubicin, methotrexate and 5-fluorouracil, for a possible therapeutic system. To verify the hypothesis that copper metallodendrimers can form conjugates with anticancer drugs, their complexes were biophysically characterized using zeta potential and zeta size methods. Next, to confirm the existence of a synergetic effect of dendrimers and drugs, in vitro studies were performed. The combination therapy has been applied in two cancer cell lines: MCF-7 (human breast cancer cell line) and HepG2 (human liver carcinoma cell line). The doxorubicin (DOX), methotrexate (MTX) and 5-fluorouracil (5-FU) were more effective against cancer cells wh</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-08-17T03:07:45.487Z</modification><creation>2024-11-09T23:53:07.581Z</creation></dates><accession>S-EPMC9960994</accession><cross_references><pubmed>36835489</pubmed><doi>10.3390/ijms24044076</doi></cross_references></HashMap>