Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add filters








Language
Year range
1.
Chinese Medical Journal ; (24): 746-749, 2002.
Article in English | WPRIM | ID: wpr-302214

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>


Subject(s)
Humans , Apoptosis , Genetics , Physiology , Carcinoma, Renal Cell , Genetics , Pathology , Cell Division , Genetics , Physiology , Cell Line , Cloning, Molecular , DNA, Antisense , Genetics , Physiology , DNA, Complementary , Chemistry , Genetics , Gene Expression Regulation, Neoplastic , Genes, Neoplasm , Genetics , Kidney Neoplasms , Genetics , Pathology , Neoplasm Proteins , Genetics , Oligonucleotides , Genetics , Sequence Analysis, DNA , Transfection , Tumor Cells, Cultured
SELECTION OF CITATIONS
SEARCH DETAIL