| Literature DB >> 29870057 |
Yong-Yan Bi1, Gang Shen1, Yong Quan1, Wei Jiang1, Fulin Xu1.
Abstract
Gliomas are the commonest and most aggressive primary malignant tumor in the central nervous system. Long noncoding RNAs (lncRNAs) have been identified to act as crucial regulators in multiple biological processes, including tumorigenesis. FAM83H antisense RNA1 (FAM83H-AS1) has been uncovered to be dysregulated in several cancers. However, the biological role of FAM83H-AS1 in glioma still needs to be investigated. Currently, our findings indicated that FAM83H-AS1 was upregulated in glioma tissues and cell lines and high level of FAM83H-AS1 was associated with poor prognosis of glioma. Loss-of-function assays demonstrated that silenced FAM83H-AS1 obviously suppressed cell proliferation via regulating the cell-cycle distribution and cell apoptosis rate, and mechanistic experiments revealed that FAM83H-AS1 could epidemically silence CDKN1A expression through recruiting EZH2 to the promoter of CDKN1A, thereby influencing the cell cycle and proliferation. Collectively, our findings suggested that FAM83H-AS1 participated in the progression of glioma and might act as a potential therapeutic target and prognosis biomarker for human glioma.Entities:
Keywords: CDKN1A; EZH2; FAM83H-AS1; H3K27me3; glioma
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Year: 2018 PMID: 29870057 DOI: 10.1002/jcp.26813
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384