2022
DOI: 10.1139/cjpp-2021-0149
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SNHG8 promotes cell proliferation, migration, and invasion of nasopharyngeal carcinoma cells as an oncogene through miR-588/HMGA2 axis

Abstract: Nasopharyngeal carcinoma (NC) poses a threat to the life of patients. Long non-coding RNA (LncRNA) is a novel kind of non-coding RNA, which plays a pivotal role through sponge microRNA (miRNA). Abnormal expression of small nucleolar RNA host gene 8 (SNHG8) is involved in various tumors; however, the role of SNHG8 in NC remains unknown. Quantitative real-time PCR (qRT-PCR) and Western blotting was employed to detect the expression levels of SNHG8, miR-588, and high mobility group A2 (HMGA2). Cell proliferation,… Show more

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Cited by 3 publications
(2 citation statements)
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“…All findings suggested that SNHG15 was promising as a biomarker and therapeutic target for cancer patients. Similarly, SNHG8 was considered to be an oncogenic factor and was upregulated in various types of cancer (Yuan et al, 2021), such as gastric cancer, melanoma, nasopharyngeal cancer, and esophageal cancer (Shan et al, 2022b;Luan et al, 2022;Wu et al, 2022;Zhu et al, 2022). LINC00471 was an essential member of the prognostic model of childhood acute myeloid leukemia and esophageal squamous cell carcinoma (Zhang et al, 2019a;Yu et al, 2019).…”
Section: Discussionmentioning
confidence: 99%
“…All findings suggested that SNHG15 was promising as a biomarker and therapeutic target for cancer patients. Similarly, SNHG8 was considered to be an oncogenic factor and was upregulated in various types of cancer (Yuan et al, 2021), such as gastric cancer, melanoma, nasopharyngeal cancer, and esophageal cancer (Shan et al, 2022b;Luan et al, 2022;Wu et al, 2022;Zhu et al, 2022). LINC00471 was an essential member of the prognostic model of childhood acute myeloid leukemia and esophageal squamous cell carcinoma (Zhang et al, 2019a;Yu et al, 2019).…”
Section: Discussionmentioning
confidence: 99%
“…Compared with the results from the combined analysis before and after exclusion, there was no significant change in the association between the high expression of lncRNAs and the T stage, N stage and clinical stage of patients with NPC. The association between the high expression of lncRNAs and the M stage of patients with NPC was affected by the data from the studies by Gao et al 2019( 22 ), Luan et al 2022( 37 ) and Nie et al 2013( 29 ); when these studies were excluded, the I 2 was reduced from 73 to 67%. The data demonstrated that the expression of lncRNAs in the M1 stage was significantly higher than that in the M0 stage (P<0.05) in patients with NPC.…”
Section: Resultsmentioning
confidence: 99%