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Long noncoding RNA OIP5-AS1 acts as a competing endogenous RNA to promote glutamine catabolism and malignant melanoma growth by sponging miR-217.
Luan, Wenkang; Zhang, Xuanfeng; Ruan, Hongru; Wang, Jinlong; Bu, Xuefeng.
Afiliação
  • Luan W; Department of Plastic Surgery, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
  • Zhang X; Department of General Surgery, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
  • Ruan H; Department of Plastic Surgery, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
  • Wang J; Department of Plastic Surgery, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
  • Bu X; Department of General Surgery, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
J Cell Physiol ; 234(9): 16609-16618, 2019 Sep.
Article em En | MEDLINE | ID: mdl-30779126
The long noncoding RNA (lncRNA) OIP5-AS1 has been considered to promote the growth and metastasis of many human tumors. However, the role of OIP5-AS1 in melanoma has not been reported. In this study, we found that OIP5-AS1 levels were significantly elevated in melanoma tissue and that high OIP5-AS1 expression was an independent risk factor for the poor survival of patients with melanoma. miR-217 suppressed glutamine catabolism in melanoma cells by targeting glutaminase (GLS), the rate-limiting enzyme of glutamine catabolism. We also demonstrated that OIP5-AS1 acted as a sponge of miR-217 to upregulate GLS expression, thus promoting glutamine catabolism and melanoma growth. Overall, this result elucidates a new mechanism for OIP5-AS1 in metabolism in melanoma and provides a potential therapeutic target for patients with melanoma.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: J Cell Physiol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: J Cell Physiol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos