<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pacak K</submitter><funding>Intramural NIH HHS</funding><pagination>2445-55</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4131300</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>131(10)</volume><pubmed_abstract>Pheochromocytomas (PHEOs) and paragangliomas (PGLs) are specific types of neuroendocrine tumors that originate in the adrenal medulla or sympathetic/parasympathetic paraganglia, respectively. Although these tumors are intensively studied, a very effective treatment for metastatic PHEO or PGL has not yet been established. Preclinical evaluations of novel therapies for these tumors are very much required. Therefore, in this study we tested the effect of triptolide (TTL), a potent nuclear factor-kappaB (NF-κB) inhibitor, on the cell membrane norepinephrine transporter (NET) system, considered to be the gatekeeper for the radiotherapeutic agent 131I-metaiodobenzylguanidine (131I-MIBG). We measured changes in the mRNA and protein levels of NET and correlated them with proapoptotic factors and m</pubmed_abstract><journal>International journal of cancer</journal><pubmed_title>NF-κB inhibition significantly upregulates the norepinephrine transporter system, causes apoptosis in pheochromocytoma cell lines and prevents metastasis in an animal model.</pubmed_title><pmcid>PMC4131300</pmcid><funding_grant_id>ZIA HD008735-09</funding_grant_id><pubmed_authors>Sirova M</pubmed_authors><pubmed_authors>Hudecova S</pubmed_authors><pubmed_authors>Giubellino A</pubmed_authors><pubmed_authors>Laukova M</pubmed_authors><pubmed_authors>Lencesova L</pubmed_authors><pubmed_authors>Csaderova L</pubmed_authors><pubmed_authors>Pacak K</pubmed_authors><pubmed_authors>Krizanova O</pubmed_authors></additional><is_claimable>false</is_claimable><name>NF-κB inhibition significantly upregulates the norepinephrine transporter system, causes apoptosis in pheochromocytoma cell lines and prevents metastasis in an animal model.</name><description>Pheochromocytomas (PHEOs) and paragangliomas (PGLs) are specific types of neuroendocrine tumors that originate in the adrenal medulla or sympathetic/parasympathetic paraganglia, respectively. Although these tumors are intensively studied, a very effective treatment for metastatic PHEO or PGL has not yet been established. Preclinical evaluations of novel therapies for these tumors are very much required. Therefore, in this study we tested the effect of triptolide (TTL), a potent nuclear factor-kappaB (NF-κB) inhibitor, on the cell membrane norepinephrine transporter (NET) system, considered to be the gatekeeper for the radiotherapeutic agent 131I-metaiodobenzylguanidine (131I-MIBG). We measured changes in the mRNA and protein levels of NET and correlated them with proapoptotic factors and m</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Nov</publication><modification>2025-04-21T15:40:01.94Z</modification><creation>2019-03-27T01:33:58Z</creation></dates><accession>S-EPMC4131300</accession><cross_references><pubmed>22407736</pubmed><doi>10.1002/ijc.27524</doi></cross_references></HashMap>