<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Monastirioti A</submitter><funding>Bristol Myers Squibb International Corporation (BMS)</funding><pagination>4739</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9564103</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(19)</volume><pubmed_abstract>Since circulating microRNAs (miRNAs) are involved in the modulation of the immune response, they are tested as liquid biopsy-based biomarkers in patients with NSCLC treated with immunotherapy. We analyzed the expression levels and examined the clinical significance of immunoregulatory miRNAs involved in immune checkpoint regulation (miR-34a, miR-200b, miR-200c), T-cell activity (miR-155), and the function of myeloid-derived suppressive cells (MDSCs) (miR-223) or regulatory T lymphocytes (Tregs) (miR-146a), in patients with advanced NSCLC (N = 69) treated with anti-PD-1 (Nivolumab) immunotherapy as 2nd or 3rd line of treatment therapy. Plasma levels of circulating miRNAs were analyzed by RT-qPCR before the initiation of immunotherapy. Expression of miR-34a, miR-146a, mir-200c, and miR-223 w</pubmed_abstract><journal>Cancers</journal><pubmed_title>Plasma-Based microRNA Expression Analysis in Advanced Stage NSCLC Patients Treated with Nivolumab.</pubmed_title><pmcid>PMC9564103</pmcid><funding_grant_id>CA209-8NX</funding_grant_id><pubmed_authors>Kalapanida D</pubmed_authors><pubmed_authors>Papadaki MA</pubmed_authors><pubmed_authors>Mavroudis D</pubmed_authors><pubmed_authors>Rounis K</pubmed_authors><pubmed_authors>Agelaki S</pubmed_authors><pubmed_authors>Michaelidou K</pubmed_authors><pubmed_authors>Monastirioti A</pubmed_authors><pubmed_authors>Papadaki C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Plasma-Based microRNA Expression Analysis in Advanced Stage NSCLC Patients Treated with Nivolumab.</name><description>Since circulating microRNAs (miRNAs) are involved in the modulation of the immune response, they are tested as liquid biopsy-based biomarkers in patients with NSCLC treated with immunotherapy. We analyzed the expression levels and examined the clinical significance of immunoregulatory miRNAs involved in immune checkpoint regulation (miR-34a, miR-200b, miR-200c), T-cell activity (miR-155), and the function of myeloid-derived suppressive cells (MDSCs) (miR-223) or regulatory T lymphocytes (Tregs) (miR-146a), in patients with advanced NSCLC (N = 69) treated with anti-PD-1 (Nivolumab) immunotherapy as 2nd or 3rd line of treatment therapy. Plasma levels of circulating miRNAs were analyzed by RT-qPCR before the initiation of immunotherapy. Expression of miR-34a, miR-146a, mir-200c, and miR-223 w</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-19T06:43:13.537Z</modification><creation>2025-04-19T06:43:13.537Z</creation></dates><accession>S-EPMC9564103</accession><cross_references><pubmed>36230658</pubmed><doi>10.3390/cancers14194739</doi></cross_references></HashMap>