<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cao MX</submitter><funding>National Key R&amp;amp;D Program of China</funding><funding>National Natural Science Foundation of China</funding><pagination>102</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7268480</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>39(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Human papillomavirus (HPV)-positive oral squamous cell carcinoma (OSCC) is increasing worldwide with typically higher grade and stage, while better prognosis. microRNAs (miRNAs) has been shown to play a critical role in cancer, however, their role in HPV-positive OSCC progression remains unclear.&lt;h4>Methods&lt;/h4>miRNA microarray was performed to identify differentially expressed miRNAs. qRT-PCR and FISH were performed to determine the relative expression of miR-550a-3-5p. CCK-8, Flow cytometry, Wound healing, Cell invasion assays and xenograft experiments were conducted to analyze the biological roles of miR-550a-3-5p. Tumor-associated macrophages (TAMs) generation, co-culturing of cancer cells with TAMs, Western blot, Dual-luciferase reporter gene assay, Immunohistochemi</pubmed_abstract><journal>Journal of experimental &amp; clinical cancer research : CR</journal><pubmed_title>Interplay between cancer cells and M2 macrophages is necessary for miR-550a-3-5p down-regulation-mediated HPV-positive OSCC progression.</pubmed_title><pmcid>PMC7268480</pmcid><funding_grant_id>81672672, 81972542, 81902779 and 21838002</funding_grant_id><funding_grant_id>2019YFA09005700</funding_grant_id><pubmed_authors>Jiang J</pubmed_authors><pubmed_authors>Tang YL</pubmed_authors><pubmed_authors>Cao MX</pubmed_authors><pubmed_authors>Wu JS</pubmed_authors><pubmed_authors>Wu JB</pubmed_authors><pubmed_authors>Tang YJ</pubmed_authors><pubmed_authors>Qiao XW</pubmed_authors><pubmed_authors>Huang MC</pubmed_authors><pubmed_authors>Liang XH</pubmed_authors><pubmed_authors>Zhang WL</pubmed_authors><pubmed_authors>Wang K</pubmed_authors><pubmed_authors>Yu XH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Interplay between cancer cells and M2 macrophages is necessary for miR-550a-3-5p down-regulation-mediated HPV-positive OSCC progression.</name><description>&lt;h4>Background&lt;/h4>Human papillomavirus (HPV)-positive oral squamous cell carcinoma (OSCC) is increasing worldwide with typically higher grade and stage, while better prognosis. microRNAs (miRNAs) has been shown to play a critical role in cancer, however, their role in HPV-positive OSCC progression remains unclear.&lt;h4>Methods&lt;/h4>miRNA microarray was performed to identify differentially expressed miRNAs. qRT-PCR and FISH were performed to determine the relative expression of miR-550a-3-5p. CCK-8, Flow cytometry, Wound healing, Cell invasion assays and xenograft experiments were conducted to analyze the biological roles of miR-550a-3-5p. Tumor-associated macrophages (TAMs) generation, co-culturing of cancer cells with TAMs, Western blot, Dual-luciferase reporter gene assay, Immunohistochemi</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jun</publication><modification>2025-04-04T13:59:38.879Z</modification><creation>2020-06-13T07:11:09Z</creation></dates><accession>S-EPMC7268480</accession><cross_references><pubmed>32493454</pubmed><doi>10.1186/s13046-020-01602-1</doi></cross_references></HashMap>