<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>20(8)</volume><submitter>Gow CH</submitter><pubmed_abstract>A kinesin family member 5b (KIF5B)-MET proto-oncogene, receptor tyrosine kinase (MET) rearrangement was reported in patients with lung adenocarcinoma but its oncogenic function was not fully evaluated. We used one-step reverse transcription-polymerase chain reaction for RNA samples to screen for the KIF5B-MET fusion in 206 lung adenocarcinoma and 28 pulmonary sarcomatoid carcinoma patients. Genomic breakpoints of KIF5B-MET were determined by targeted next-generation sequencing. Soft agar colony formation assays, proliferation assays, and a xenograft mouse model were used to investigate its oncogenic activity. In addition, specific MET inhibitors were administered to evaluate their anti-tumor activities. A KIF5B-MET fusion variant in a patient with a mixed-type adenocarcinoma and sarcomatoi</pubmed_abstract><journal>Neoplasia (New York, N.Y.)</journal><pagination>838-847</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6068088</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Oncogenic Function of a KIF5B-MET Fusion Variant in Non-Small Cell Lung Cancer.</pubmed_title><pmcid>PMC6068088</pmcid><pubmed_authors>Liu YN</pubmed_authors><pubmed_authors>Tsai TH</pubmed_authors><pubmed_authors>Chen PL</pubmed_authors><pubmed_authors>Hsieh MS</pubmed_authors><pubmed_authors>Chang SH</pubmed_authors><pubmed_authors>Li HY</pubmed_authors><pubmed_authors>Gow CH</pubmed_authors><pubmed_authors>Tsai MF</pubmed_authors><pubmed_authors>Luo SC</pubmed_authors><pubmed_authors>Shih JY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Oncogenic Function of a KIF5B-MET Fusion Variant in Non-Small Cell Lung Cancer.</name><description>A kinesin family member 5b (KIF5B)-MET proto-oncogene, receptor tyrosine kinase (MET) rearrangement was reported in patients with lung adenocarcinoma but its oncogenic function was not fully evaluated. We used one-step reverse transcription-polymerase chain reaction for RNA samples to screen for the KIF5B-MET fusion in 206 lung adenocarcinoma and 28 pulmonary sarcomatoid carcinoma patients. Genomic breakpoints of KIF5B-MET were determined by targeted next-generation sequencing. Soft agar colony formation assays, proliferation assays, and a xenograft mouse model were used to investigate its oncogenic activity. In addition, specific MET inhibitors were administered to evaluate their anti-tumor activities. A KIF5B-MET fusion variant in a patient with a mixed-type adenocarcinoma and sarcomatoi</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Aug</publication><modification>2025-04-04T20:30:45.843Z</modification><creation>2019-03-26T23:49:11Z</creation></dates><accession>S-EPMC6068088</accession><cross_references><pubmed>30015159</pubmed><doi>10.1016/j.neo.2018.06.007</doi></cross_references></HashMap>