<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(7)</volume><submitter>Ma YS</submitter><pubmed_abstract>Increasing evidence supports that microRNA (miRNA) plays a significant functional role in cancer progression by directly regulating respective targets. In this study, the expression levels of miR-105-1 and its target gene were analyzed using genes microarray and hierarchical clustering analysis followed by validation with quantitative RT-PCR in hepatocellular carcinoma (HCC) and normal liver tissues. We examined the expression of nuclear receptor coactivator 1 (NCOA1), the potential target gene of miR-105-1, following the transfection of miR-105-1 mimics or inhibitors. Our results showed that miR-105-1 was downregulated in HCC tissues when compared with normal liver tissues and patients with lower miR-105-1 expression had shorter overall survival (OS) and progression free survival (PFS). M</pubmed_abstract><journal>Oncotarget</journal><pagination>11896-11905</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5355313</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>High expression of miR-105-1 positively correlates with clinical prognosis of hepatocellular carcinoma by targeting oncogene NCOA1.</pubmed_title><pmcid>PMC5355313</pmcid><pubmed_authors>Zhong XJ</pubmed_authors><pubmed_authors>Chai L</pubmed_authors><pubmed_authors>Wu TM</pubmed_authors><pubmed_authors>Yang HQ</pubmed_authors><pubmed_authors>Cong XL</pubmed_authors><pubmed_authors>Lu GX</pubmed_authors><pubmed_authors>Xie RT</pubmed_authors><pubmed_authors>Ma YS</pubmed_authors><pubmed_authors>Chang ZY</pubmed_authors><pubmed_authors>Fu D</pubmed_authors><pubmed_authors>Zhu J</pubmed_authors><pubmed_authors>Lv ZW</pubmed_authors><pubmed_authors>Sun R</pubmed_authors><pubmed_authors>Cai MX</pubmed_authors></additional><is_claimable>false</is_claimable><name>High expression of miR-105-1 positively correlates with clinical prognosis of hepatocellular carcinoma by targeting oncogene NCOA1.</name><description>Increasing evidence supports that microRNA (miRNA) plays a significant functional role in cancer progression by directly regulating respective targets. In this study, the expression levels of miR-105-1 and its target gene were analyzed using genes microarray and hierarchical clustering analysis followed by validation with quantitative RT-PCR in hepatocellular carcinoma (HCC) and normal liver tissues. We examined the expression of nuclear receptor coactivator 1 (NCOA1), the potential target gene of miR-105-1, following the transfection of miR-105-1 mimics or inhibitors. Our results showed that miR-105-1 was downregulated in HCC tissues when compared with normal liver tissues and patients with lower miR-105-1 expression had shorter overall survival (OS) and progression free survival (PFS). M</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Feb</publication><modification>2025-04-19T07:59:51.271Z</modification><creation>2019-06-06T17:10:24Z</creation></dates><accession>S-EPMC5355313</accession><cross_references><pubmed>28060733</pubmed><doi>10.18632/oncotarget.14435</doi></cross_references></HashMap>