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Renal cell carcinoma related novel gene, GYLZ-RCC18: cloning and functional studies / 中华医学杂志(英文版)
Chinese Medical Journal ; (24): 746-749, 2002.
Article en En | WPRIM | ID: wpr-302214
Biblioteca responsable: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To clone the full length of renal cell carcinoma (RCC) related novel gene GYLZ-RCC18 and study its function.</p><p><b>METHODS</b>SMART RACE technology was used to clone the full length of GYLZ-RCC18. RT-PCR was used to detect its expression in renal cell carcinoma tissue at different stages and grades. We transfected the antisense oligonucleotide of GYLZ-RCC18 to renal cell carcinoma cell line, GRC-1, and analyzed proliferation activity, growth rate, apoptosis, and mortality changes.</p><p><b>RESULTS</b>The full length of GYLZ-RCC18 (GenBank accession number: BE825133) cDNA was about 3.5 kb. GYLZ-RCC18 had a higher expression in higher grades and stages of renal cell carcinoma than in lower ones. The expression of GYLZ-RCC18 in renal cell carcinoma was much higher than in normal kidney. After the transfection of GYLZ-RCC18 antisense oligonucleotide, the mortality of GRC-1 increased significantly, while proliferative activity and growth rate were substantially inhibited at the same time. The antisense oligonucleotide induced apoptosis of GRC-1 through the entire observation time.</p><p><b>CONCLUSION</b>GYLZ-RCC18 is an important novel gene related to renal cell carcinoma. Overexpression of this gene results in higher growth and proliferative activity and has an antiapoptosis effect on renal cell carcinoma cells. Transfection of the antisense oligonucleotide may inhibit the generation and development of renal cell carcinoma.</p>
Asunto(s)
Texto completo: 1 Índice: WPRIM Asunto principal: Oligonucleótidos / Patología / Fisiología / Células Tumorales Cultivadas / Carcinoma de Células Renales / Transfección / Regulación Neoplásica de la Expresión Génica / División Celular / Línea Celular / Química Límite: Humans Idioma: En Revista: Chinese Medical Journal Año: 2002 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Oligonucleótidos / Patología / Fisiología / Células Tumorales Cultivadas / Carcinoma de Células Renales / Transfección / Regulación Neoplásica de la Expresión Génica / División Celular / Línea Celular / Química Límite: Humans Idioma: En Revista: Chinese Medical Journal Año: 2002 Tipo del documento: Article