Your browser doesn't support javascript.
loading
Long Non-coding RNA JHDM1D-AS1 Interacts with DHX15 Protein to Enhance Non-Small-Cell Lung Cancer Growth and Metastasis.
Yao, Guodong; Chen, Kexin; Qin, Yu; Niu, Yangyang; Zhang, Xuefang; Xu, Shidong; Zhang, Chi; Feng, Meiyan; Wang, Kuan.
Afiliação
  • Yao G; Department of Pathology, Harbin Medical University Cancer Hospital, Harbin, China.
  • Chen K; Department of Pathology, Harbin Medical University Cancer Hospital, Harbin, China.
  • Qin Y; Department of Pathology, Harbin Medical University Cancer Hospital, Harbin, China.
  • Niu Y; Department of Pathology, Harbin Medical University Cancer Hospital, Harbin, China.
  • Zhang X; Department of Pathology, Harbin Medical University Cancer Hospital, Harbin, China.
  • Xu S; Department of Thoracic Surgery, Harbin Medical University Cancer Hospital, Harbin, China.
  • Zhang C; Brandeis University, Waltham, MA, USA.
  • Feng M; Department of Pathology, Harbin Medical University Cancer Hospital, Harbin, China. Electronic address: meiy_feng@163.com.
  • Wang K; Department of Gastrointestinal Surgery, Harbin Medical University Cancer Hospital, Harbin, China. Electronic address: 88008008@sina.com.
Mol Ther Nucleic Acids ; 18: 831-840, 2019 Dec 06.
Article em En | MEDLINE | ID: mdl-31739208
JHDM1D antisense 1 (JHDM1D-AS1), a long non-coding RNA (lncRNA), has been shown to promote pancreatic cancer growth by inducing an angiogenic response. However, its biological and clinical significance in non-small-cell lung cancer (NSCLC) is still unclear. In this study, we examined the expression and prognostic significance of JHDM1D-AS1 in NSCLC. The effects of JHDM1D-AS1 knockdown or overexpression on NSCLC growth and metastasis were investigated. We show that JHDM1D-AS1 is upregulated in NSCLC relative to adjacent normal lung tissues. High JHDM1D-AS1 expression is significantly correlated with advanced tumor, node, and metastasis (TNM) stage and lymph node metastasis. JHDM1D-AS1 expression serves as an independent prognostic factor for overall survival of patients with NSCLC. Functionally, JHDM1D-AS1 knockdown inhibits NSCLC cell aggressiveness both in vitro and in vivo, which is rescued by ectopic expression of JHDM1D-AS1. JHDM1D-AS1 binding stabilizes DHX15 protein in NSCLC cells. DHX15 overexpression enhances NSCLC cell proliferation and invasion, whereas knockdown of DHX15 exerts opposite effects. JHDM1D-AS1-mediated aggressive phenotype is impaired when DHX15 is silenced. Ectopic expression of DHX15 restores the defects in proliferation and invasion of JHDM1D-AS1-depleted NSCLC cells. Collectively, the interaction between JHDM1D-AS1 and DHX15 accounts for NSCLC growth and metastasis. This work provides potential additional therapeutic targets for treatment of NSCLC.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2019 Tipo de documento: Article