Your browser doesn't support javascript.
loading
Suppression of the long non-coding RNA MALAT-1 impairs the growth and migration of human tongue squamous cell carcinoma SCC4 cells.
Han, Xu; Xu, Zixiao; Tian, Gang; Tang, Zhen; Gao, JianYong; Wei, Yibo; Xu, XiaoGang.
Afiliação
  • Han X; Department of Stomatology, Changhai Hospital Affiliated to Second Military Medical University, Shanghai, China.
  • Xu Z; Department of Stomatology, Changhai Hospital Affiliated to Second Military Medical University, Shanghai, China.
  • Tian G; Department of Stomatology, Changhai Hospital Affiliated to Second Military Medical University, Shanghai, China.
  • Tang Z; Department of Stomatology, Changhai Hospital Affiliated to Second Military Medical University, Shanghai, China.
  • Gao J; Department of Stomatology, Changhai Hospital Affiliated to Second Military Medical University, Shanghai, China.
  • Wei Y; Department of Stomatology, Changhai Hospital Affiliated to Second Military Medical University, Shanghai, China.
  • Xu X; Department of Stomatology, Changhai Hospital Affiliated to Second Military Medical University, Shanghai, China.
Arch Med Sci ; 15(4): 992-1000, 2019 Jul.
Article em En | MEDLINE | ID: mdl-31360193
INTRODUCTION: Aberrant expression of long non-coding RNAs (lncRNAs) is associated with metastasis and poor prognosis in patients with various cancer types. However, few studies have assessed lncRNAs in oral squamous cell carcinoma (OSCC). This study aimed to investigate the expression and impact of lncRNAs in OSCC. MATERIAL AND METHODS: Real-time PCR analysis was used to examine the expression of four lncRNAs, MALAT-1, UCA1, BC200 and SRA, in 14 OSCC and adjacent normal tissue pairs. The impact of MALAT-1 suppression by siRNA on the proliferation, apoptosis, anchorage-independent growth and migration of the human tongue carcinoma cell line SSC4 was also determined. RESULTS: MALAT-1 levels were significantly higher in the OSCC tissue than in the normal tissues (p < 0.004); no significant differences in UCA1, BC200 or SRA RNA levels were observed. Knockdown of MALAT-1 by siRNA significantly suppressed proliferation of SSC4 cells (p < 0.004) and enhanced their apoptosis (p < 0.001). In addition, siRNA-mediated suppression of MALAT-1 inhibited SSC4 cell colony formation (p < 0.001) and migration (p < 0.004). CONCLUSIONS: Elevated expression of MALAT-1 in OSCC may play a role in tumorigenesis and/or metastasis. Further studies are necessary to identify the mechanism by which MALAT-1 influences SCC4 growth and migration and validate its increased expression in OSCC patients.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Arch Med Sci Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China País de publicação: Polônia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Arch Med Sci Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China País de publicação: Polônia