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LncRNA THOR promotes human renal cell carcinoma cell growth.
Ye, Xue-Ting; Huang, Hang; Huang, Wei-Ping; Hu, Wei-Lie.
Afiliación
  • Ye XT; Graduate School, Southern Medical University, Guangzhou, China; Department of Urology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Huang H; Department of Urology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Huang WP; Department of Urology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Hu WL; Graduate School, Southern Medical University, Guangzhou, China; Department of Urology, Guangzhou General Hospital of Guangzhou Military Command, Guangzhou, China. Electronic address: profhu_weilie@163.com.
Biochem Biophys Res Commun ; 501(3): 661-667, 2018 06 27.
Article en En | MEDLINE | ID: mdl-29752937
BACKGROUND: Recent studies have characterized a novel but extremely conserved long non-coding RNA (LncRNA) THOR. THOR directly associates with insulin-like growth factor 2 mRNA-binding protein 1 (IGF2BP1) to promote mRNA stabilization of key pro-cancerous genes. RESULTS: Here, we show that THOR is expressed in human renal cell carcinoma (RCC) tissues and established/primary human RCC cells. It was not detected in normal renal tissues nor in HK-2 and primary human renal epithelial cells. THOR silencing (by targeted siRNAs) or CRISPR/Cas9 knockout inhibited RCC cell growth, viability and proliferation in vitro. Reversely, forced over-expression of THOR promoted RCC cell survival and proliferation. IGF2BP1-regulated genes, including IGF2, GLI1 and Myc, were downregulated by THOR silencing or knockout, but they were upregulated after THOR over-expression. In vivo, THOR-knockout 786-O tumors grew significantly slower than the control tumors in nude mice. CONCLUSION: THOR expression promotes RCC cell growth in vitro and in vivo. THOR could be a novel and important therapeutic target for human RCC.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Células Renales / Regulación Neoplásica de la Expresión Génica / ARN Largo no Codificante / Neoplasias Renales Límite: Adult / Aged / Animals / Humans / Male / Middle aged Idioma: En Revista: Biochem Biophys Res Commun Año: 2018 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Células Renales / Regulación Neoplásica de la Expresión Génica / ARN Largo no Codificante / Neoplasias Renales Límite: Adult / Aged / Animals / Humans / Male / Middle aged Idioma: En Revista: Biochem Biophys Res Commun Año: 2018 Tipo del documento: Article País de afiliación: China Pais de publicación: Estados Unidos