<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(5)</volume><submitter>Harter PN</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Current pathological diagnostics include the analysis of (epi-)genetic alterations as well as oncogenic pathways. Deregulated mammalian target of rapamycin complex 1 (mTORC1) signaling has been implicated in a variety of cancers including malignant gliomas and is considered a promising target in cancer treatment. Monitoring of mTORC1 activity before and during inhibitor therapy is essential. The aim of our study is to provide a recommendation and report on pitfalls in the use of phospho-specific antibodies against mTORC1-targets phospho-RPS6 (Ser235/236; Ser240/244) and phospho-4EBP1 (Thr37/46) in formalin fixed, paraffin embedded material.&lt;h4>Methods and findings&lt;/h4>Primary, established cell lines and brain tumor tissue from routine diagnostics were assessed by immunoc</pubmed_abstract><journal>PloS one</journal><pagination>e0127123</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4437987</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Immunohistochemical Assessment of Phosphorylated mTORC1-Pathway Proteins in Human Brain Tumors.</pubmed_title><pmcid>PMC4437987</pmcid><pubmed_authors>Senft C</pubmed_authors><pubmed_authors>Ronellenfitsch MW</pubmed_authors><pubmed_authors>Ilina E</pubmed_authors><pubmed_authors>Baumgarten P</pubmed_authors><pubmed_authors>Tichy J</pubmed_authors><pubmed_authors>Thiepold AL</pubmed_authors><pubmed_authors>Steinbach JP</pubmed_authors><pubmed_authors>Zornig M</pubmed_authors><pubmed_authors>Burger MC</pubmed_authors><pubmed_authors>Harter PN</pubmed_authors><pubmed_authors>Jennewein L</pubmed_authors><pubmed_authors>Mittelbronn M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immunohistochemical Assessment of Phosphorylated mTORC1-Pathway Proteins in Human Brain Tumors.</name><description>&lt;h4>Background&lt;/h4>Current pathological diagnostics include the analysis of (epi-)genetic alterations as well as oncogenic pathways. Deregulated mammalian target of rapamycin complex 1 (mTORC1) signaling has been implicated in a variety of cancers including malignant gliomas and is considered a promising target in cancer treatment. Monitoring of mTORC1 activity before and during inhibitor therapy is essential. The aim of our study is to provide a recommendation and report on pitfalls in the use of phospho-specific antibodies against mTORC1-targets phospho-RPS6 (Ser235/236; Ser240/244) and phospho-4EBP1 (Thr37/46) in formalin fixed, paraffin embedded material.&lt;h4>Methods and findings&lt;/h4>Primary, established cell lines and brain tumor tissue from routine diagnostics were assessed by immunoc</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015</publication><modification>2026-04-19T03:22:58.488Z</modification><creation>2019-03-26T23:32:50Z</creation></dates><accession>S-EPMC4437987</accession><cross_references><pubmed>25993328</pubmed><doi>10.1371/journal.pone.0127123</doi></cross_references></HashMap>