<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(10)</volume><submitter>Lei Y</submitter><pubmed_abstract>B-cell-specific Moloney murine leukemia virus integration site 1 (Bmi-1) is overexpressed in various cancer types. We found that &lt;i>Bmi-1&lt;/i> mRNA levels were elevated in nasopharyngeal carcinoma (NPC) cell lines. In immunohistochemical analyses, high Bmi-1 levels were observed in not only 5 of 38 non-cancerous nasopharyngeal squamous epithelial biopsies, but also in 66 of 98 NPC specimens (67.3%). High Bmi-1 levels were detected more frequently in T3-T4, N2-N3 and stage III-IV NPC biopsies than in T1-T2, N0-N1 and stage I-II NPC samples, indicating that Bmi-1 is upregulated in advanced NPC. In 5-8F and SUNE1 NPC cells, stable depletion of Bmi-1 using lentiviral RNA interference greatly suppressed cell proliferation, induced G1-phase cell cycle arrest, reduced cell stemness and suppressed </pubmed_abstract><journal>Aging</journal><pagination>4391-4410</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10258013</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Hairy gene homolog increases nasopharyngeal carcinoma cell stemness by upregulating &lt;i>Bmi-1&lt;/i>.</pubmed_title><pmcid>PMC10258013</pmcid><pubmed_authors>Zhou ZH</pubmed_authors><pubmed_authors>He DH</pubmed_authors><pubmed_authors>Xia JW</pubmed_authors><pubmed_authors>Xiao SJ</pubmed_authors><pubmed_authors>Lin XL</pubmed_authors><pubmed_authors>Chen ML</pubmed_authors><pubmed_authors>Wang SC</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors><pubmed_authors>Li XF</pubmed_authors><pubmed_authors>Dai GQ</pubmed_authors><pubmed_authors>Cong JG</pubmed_authors><pubmed_authors>Li YC</pubmed_authors><pubmed_authors>Zhang XK</pubmed_authors><pubmed_authors>Li QW</pubmed_authors><pubmed_authors>Lei Y</pubmed_authors><pubmed_authors>Xie HT</pubmed_authors><pubmed_authors>Huang SH</pubmed_authors><pubmed_authors>Wu AB</pubmed_authors><pubmed_authors>Xiao D</pubmed_authors><pubmed_authors>Yang S</pubmed_authors><pubmed_authors>Jia JS</pubmed_authors><pubmed_authors>Shen HF</pubmed_authors><pubmed_authors>Lin TY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hairy gene homolog increases nasopharyngeal carcinoma cell stemness by upregulating &lt;i>Bmi-1&lt;/i>.</name><description>B-cell-specific Moloney murine leukemia virus integration site 1 (Bmi-1) is overexpressed in various cancer types. We found that &lt;i>Bmi-1&lt;/i> mRNA levels were elevated in nasopharyngeal carcinoma (NPC) cell lines. In immunohistochemical analyses, high Bmi-1 levels were observed in not only 5 of 38 non-cancerous nasopharyngeal squamous epithelial biopsies, but also in 66 of 98 NPC specimens (67.3%). High Bmi-1 levels were detected more frequently in T3-T4, N2-N3 and stage III-IV NPC biopsies than in T1-T2, N0-N1 and stage I-II NPC samples, indicating that Bmi-1 is upregulated in advanced NPC. In 5-8F and SUNE1 NPC cells, stable depletion of Bmi-1 using lentiviral RNA interference greatly suppressed cell proliferation, induced G1-phase cell cycle arrest, reduced cell stemness and suppressed </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-06-01T00:25:57.724Z</modification><creation>2025-06-01T00:25:57.724Z</creation></dates><accession>S-EPMC10258013</accession><cross_references><pubmed>37219449</pubmed><doi>10.18632/aging.204742</doi></cross_references></HashMap>