<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>35(3)</volume><submitter>Sun L</submitter><pubmed_abstract>&lt;h4>Aim&lt;/h4>To investigate the effects of serum deprivation (SD) on microvesicles (MVs) secreted from human myeloma cells and the implications for disease progression.&lt;h4>Methods&lt;/h4>RPMI 8226, U266, and KM3 human myeloma cells were incubated in medium containing 10% (non-SD) or 1% fetal bovine serum (SD) and MVs were isolated. The levels and size distribution of MVs were analyzed with flow cytometry. The protein profiles of MVs were studied using 2D SDS-PAGE, MALDI-TOF-MS, and Western blotting. NF-κB activation was analyzed using EMSA. Angiogenesis was examined in Eahy926 endothelial cells.&lt;h4>Results&lt;/h4>Exposure of RPMI 8226 cells to SD for 24 h did not alter the number of apoptotic cells. However, SD increased the number of MVs from RPMI 8226, U266, and KM3 cells to 2.5-, 4.3-, and 3.8</pubmed_abstract><journal>Acta pharmacologica Sinica</journal><pagination>381-93</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4647891</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Serum deprivation elevates the levels of microvesicles with different size distributions and selectively enriched proteins in human myeloma cells in vitro.</pubmed_title><pmcid>PMC4647891</pmcid><pubmed_authors>Sun L</pubmed_authors><pubmed_authors>Chen ZC</pubmed_authors><pubmed_authors>Wu PH</pubmed_authors><pubmed_authors>Chen WQ</pubmed_authors><pubmed_authors>Zhu XJ</pubmed_authors><pubmed_authors>Zou P</pubmed_authors><pubmed_authors>Li QB</pubmed_authors><pubmed_authors>Wang HX</pubmed_authors></additional><is_claimable>false</is_claimable><name>Serum deprivation elevates the levels of microvesicles with different size distributions and selectively enriched proteins in human myeloma cells in vitro.</name><description>&lt;h4>Aim&lt;/h4>To investigate the effects of serum deprivation (SD) on microvesicles (MVs) secreted from human myeloma cells and the implications for disease progression.&lt;h4>Methods&lt;/h4>RPMI 8226, U266, and KM3 human myeloma cells were incubated in medium containing 10% (non-SD) or 1% fetal bovine serum (SD) and MVs were isolated. The levels and size distribution of MVs were analyzed with flow cytometry. The protein profiles of MVs were studied using 2D SDS-PAGE, MALDI-TOF-MS, and Western blotting. NF-κB activation was analyzed using EMSA. Angiogenesis was examined in Eahy926 endothelial cells.&lt;h4>Results&lt;/h4>Exposure of RPMI 8226 cells to SD for 24 h did not alter the number of apoptotic cells. However, SD increased the number of MVs from RPMI 8226, U266, and KM3 cells to 2.5-, 4.3-, and 3.8</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Mar</publication><modification>2025-04-22T15:10:37.154Z</modification><creation>2019-03-27T02:02:05Z</creation></dates><accession>S-EPMC4647891</accession><cross_references><pubmed>24374813</pubmed><doi>10.1038/aps.2013.166</doi></cross_references></HashMap>