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Long noncoding RNA FAM83H-AS1 exerts an oncogenic role in glioma through epigenetically silencing CDKN1A (p21).
Bi, Yong-Yan; Shen, Gang; Quan, Yong; Jiang, Wei; Xu, Fulin.
Afiliação
  • Bi YY; Department of Neurosurgery, Minhang Hospital, Fudan University, Shanghai, China.
  • Shen G; Department of Neurosurgery, Minhang Hospital, Fudan University, Shanghai, China.
  • Quan Y; Department of Neurosurgery, Minhang Hospital, Fudan University, Shanghai, China.
  • Jiang W; Department of Neurosurgery, Minhang Hospital, Fudan University, Shanghai, China.
  • Xu F; Department of Neurosurgery, Minhang Hospital, Fudan University, Shanghai, China.
J Cell Physiol ; 233(11): 8896-8907, 2018 11.
Article em En | MEDLINE | ID: mdl-29870057
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidor de Quinase Dependente de Ciclina p21 / RNA Longo não Codificante / Proteína Potenciadora do Homólogo 2 de Zeste / Glioma Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Cell Physiol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidor de Quinase Dependente de Ciclina p21 / RNA Longo não Codificante / Proteína Potenciadora do Homólogo 2 de Zeste / Glioma Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Cell Physiol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China