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The lncRNA SNHG16 affects prognosis in hepatocellular carcinoma by regulating p62 expression.
- Source :
-
Journal of cellular physiology [J Cell Physiol] 2020 Feb; Vol. 235 (2), pp. 1090-1102. Date of Electronic Publication: 2019 Jun 29. - Publication Year :
- 2020
-
Abstract
- Long noncoding RNAs (lncRNAs) regulate tumor development and progression by promoting proliferation, invasion, and metastasis. The oncogenic role of lncRNA SNHG16 in hepatocellular carcinoma (HCC) has not been revealed. LncRNA SNHG16 is upregulated in HCC and correlates with poorer prognosis. Patients with high SNHG16 expression showed lower rates of overall and disease-free survival than patients with low SNHG16 expression. Multivariate Cox regression revealed that SNHG16 expression was an independent predictor of poor overall and disease-free survival. In vitro, SNHG16 promoted HCC cell proliferation, migration, and invasion while inhibiting apoptosis; in vivo, it accelerated tumor development. Altering SNHG16 expression altered levels of miR-17-5p, which in turn modified expression of p62, which has been shown to regulate the mTOR and NF-κB pathways. Indeed, altering SNHG16 expression in HCC cells activated mTOR and NF-κB signaling. These results reveal a potential mechanism for the oncogenic role of SNHG16 in HCC. SNHG16 may therefore be a promising diagnostic marker as well as therapeutic target in HCC.<br /> (© 2019 Wiley Periodicals, Inc.)
- Subjects :
- Adult
Aged
Carcinoma, Hepatocellular pathology
Cell Line, Tumor
Cell Movement
Female
Gene Expression Regulation, Neoplastic drug effects
Hepatocytes
Humans
Liver Neoplasms genetics
Liver Neoplasms pathology
Male
MicroRNAs genetics
MicroRNAs metabolism
Middle Aged
NF-kappa B antagonists & inhibitors
NF-kappa B genetics
NF-kappa B metabolism
Prognosis
RNA, Long Noncoding genetics
RNA-Binding Proteins genetics
Carcinoma, Hepatocellular metabolism
Gene Expression Regulation, Neoplastic physiology
Liver Neoplasms metabolism
RNA, Long Noncoding metabolism
RNA-Binding Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4652
- Volume :
- 235
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Journal of cellular physiology
- Publication Type :
- Academic Journal
- Accession number :
- 31256427
- Full Text :
- https://doi.org/10.1002/jcp.29023