作者: Sven Hillinger , Thomas Wiedl , Stephane Collaud , Stephan Arni , Peter Schraml
DOI: 10.1164/AJRCCM-CONFERENCE.2012.185.1_MEETINGABSTRACTS.A6360
关键词:
摘要: Lung cancer is the leading cause of all deaths worldwide with suboptimal prognosis and treatment options. Therefore this study aimed to identify molecular characteristics a predictive clinical utility which at same time might represent novel therapeutic targets for human lung adenocarcinoma. Within mutations v-Ki-RAS2 Kirsten rat sarcoma viral oncogene homolog (KRAS), gene frequently mutated in adenocarcinoma, their association enzymatic activities, as assessed by activity-based proteomics, members serine hydrolase (SH) superfamily, large class enzymes that have previously been linked was investigated. The results revealed activity myeloblastin significantly altered adenocarcinoma biopsies harboring KRAS mutation. In conclusion potential target indicating combination proteomics mutational analysis valid approach discovery biomarkers.