<HashMap><database>biostudies-literature</database><scores/><additional><submitter>VanCleave A</submitter><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>2597-2610</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7343631</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(27)</volume><pubmed_abstract>Outcomes have not improved for metastatic osteosarcoma for several decades. In part, this failure to develop better therapies stems from a lack of understanding of osteosarcoma biology, given the rarity of the disease and the high genetic heterogeneity at the time of diagnosis. We report here the successful establishment of a new human osteosarcoma cell line, COS-33, from a patient-derived xenograft and demonstrate retention of the biological features of the original tumor. We found high mTOR signaling activity in the cultured cells, which were sensitive to a small molecule inhibitor, rapamycin, a suppressor of the mTOR pathway. Suppressed mTOR signaling after treatment with rapamycin was confirmed by decreased phosphorylation of the S6 ribosomal protein. Increasing concentrations of rapam</pubmed_abstract><journal>Oncotarget</journal><pubmed_title>Development and characterization of the novel human osteosarcoma cell line COS-33 with sustained activation of the mTOR pathway.</pubmed_title><pmcid>PMC7343631</pmcid><funding_grant_id>P30 CA042014</funding_grant_id><funding_grant_id>P20 GM103548</funding_grant_id><funding_grant_id>P20 GM103620</funding_grant_id><pubmed_authors>Ross A</pubmed_authors><pubmed_authors>Rao P</pubmed_authors><pubmed_authors>Tao J</pubmed_authors><pubmed_authors>Torres H</pubmed_authors><pubmed_authors>Fang F</pubmed_authors><pubmed_authors>Zheng S</pubmed_authors><pubmed_authors>Li Q</pubmed_authors><pubmed_authors>Evans C</pubmed_authors><pubmed_authors>Fuglsby K</pubmed_authors><pubmed_authors>Rodezno T</pubmed_authors><pubmed_authors>Leiferman P</pubmed_authors><pubmed_authors>Palmer M</pubmed_authors><pubmed_authors>Afeworki Y</pubmed_authors><pubmed_authors>Houghton P</pubmed_authors><pubmed_authors>VanCleave A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development and characterization of the novel human osteosarcoma cell line COS-33 with sustained activation of the mTOR pathway.</name><description>Outcomes have not improved for metastatic osteosarcoma for several decades. In part, this failure to develop better therapies stems from a lack of understanding of osteosarcoma biology, given the rarity of the disease and the high genetic heterogeneity at the time of diagnosis. We report here the successful establishment of a new human osteosarcoma cell line, COS-33, from a patient-derived xenograft and demonstrate retention of the biological features of the original tumor. We found high mTOR signaling activity in the cultured cells, which were sensitive to a small molecule inhibitor, rapamycin, a suppressor of the mTOR pathway. Suppressed mTOR signaling after treatment with rapamycin was confirmed by decreased phosphorylation of the S6 ribosomal protein. Increasing concentrations of rapam</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2026-04-29T08:44:37.014Z</modification><creation>2021-02-19T22:03:42Z</creation></dates><accession>S-EPMC7343631</accession><cross_references><pubmed>32676162</pubmed><doi>10.18632/oncotarget.27611</doi></cross_references></HashMap>