<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(6)</volume><submitter>Holzhauser S</submitter><pubmed_abstract>Human papillomavirus positive (HPV&lt;sup>+&lt;/sup>) tonsillar and base of tongue squamous cell carcinoma (TSCC/BOTSCC) have better outcomes than corresponding HPV&lt;sup>-&lt;/sup> negative (HPV&lt;sup>-&lt;/sup>) cancer cases. Our previous study demonstrated that fibroblast growth factor receptor 3 (FGFR3) and phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit a (PIK3CA) are often mutated in HPV&lt;sup>+&lt;/sup> cancer. To investigate whether targeted therapy is an option for TSCC/BOTSCC, two HPV&lt;sup>+&lt;/sup> and one HPV&lt;sup>-&lt;/sup> TSCC/BOTSCC cell lines were tested for their sensitivity towards FGFR and PI3K inhibitors. The HPV&lt;sup>+&lt;/sup> cell lines UM-SCC-47 and UPCI-SCC-154, and the HPV&lt;sup>-&lt;/sup> cell line UT-SSC-60A were tested by competitive allele-specific TaqMan-PCR for presence/absenc</pubmed_abstract><journal>Oncology letters</journal><pagination>6249-6260</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6865836</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&lt;i>In vitro&lt;/i> antitumor effects of FGFR and PI3K inhibitors on human papillomavirus positive and negative tonsillar and base of tongue cancer cell lines.</pubmed_title><pmcid>PMC6865836</pmcid><pubmed_authors>Kostopoulou ON</pubmed_authors><pubmed_authors>Bersani C</pubmed_authors><pubmed_authors>Ohmayer A</pubmed_authors><pubmed_authors>Wickstrom M</pubmed_authors><pubmed_authors>Ramqvist T</pubmed_authors><pubmed_authors>Holzhauser S</pubmed_authors><pubmed_authors>Andonova T</pubmed_authors><pubmed_authors>Dalianis T</pubmed_authors><pubmed_authors>Lange BKA</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;i>In vitro&lt;/i> antitumor effects of FGFR and PI3K inhibitors on human papillomavirus positive and negative tonsillar and base of tongue cancer cell lines.</name><description>Human papillomavirus positive (HPV&lt;sup>+&lt;/sup>) tonsillar and base of tongue squamous cell carcinoma (TSCC/BOTSCC) have better outcomes than corresponding HPV&lt;sup>-&lt;/sup> negative (HPV&lt;sup>-&lt;/sup>) cancer cases. Our previous study demonstrated that fibroblast growth factor receptor 3 (FGFR3) and phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit a (PIK3CA) are often mutated in HPV&lt;sup>+&lt;/sup> cancer. To investigate whether targeted therapy is an option for TSCC/BOTSCC, two HPV&lt;sup>+&lt;/sup> and one HPV&lt;sup>-&lt;/sup> TSCC/BOTSCC cell lines were tested for their sensitivity towards FGFR and PI3K inhibitors. The HPV&lt;sup>+&lt;/sup> cell lines UM-SCC-47 and UPCI-SCC-154, and the HPV&lt;sup>-&lt;/sup> cell line UT-SSC-60A were tested by competitive allele-specific TaqMan-PCR for presence/absenc</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Dec</publication><modification>2025-04-22T00:27:56.386Z</modification><creation>2025-04-05T19:33:35.145Z</creation></dates><accession>S-EPMC6865836</accession><cross_references><pubmed>31788102</pubmed><doi>10.3892/ol.2019.10973</doi></cross_references></HashMap>