After the renal cell carcinoma related novel gene fragment GYLZ-RCC18 was c
loned by using suppression subtractive hybridization (SSH), we used the SMA
RT RACE technology to clone the full length of GYLZ-RCC18 and performed chr
omosome location by the FISH method. RT-PCR was used to detect the expressi
on of the first reading frame of GYLZ-RCC18 in different stages and grades
of renal cell carcinoma tissue and other tissues. Also we transfected the a
ntisense oligonucleotide of GYLZ-RCC18 to renal cell carcinoma cell line GR
C-1, and analyzed the proliferation activity, growth speed, apoptosis and m
ortality changes in GRC-1. The results show that the full length of GYLZ-RC
C18 (GenBank accession No.: BE825133) cDNA is about 3.5 kb long which is lo
cated at No. 14 chromosome. GYLZ-RCC18 has a higher expression in higher gr
ades and stages of renal cell carcinoma than in the lower ones. The express
ion of GYLZ-RCC18 in renal cell carcinoma was much higher than that in norm
al kidney and other tissues. After transfection of GYLZ-RCC18 antisense oli
gonucleotide, the mortality of GRC-1 increases evidently, the proliferation
activity and growth speed were inhibited remarkably at the same time. Also
the antisense oligonucleotide can induce the apoptosis of GRC-1 all throug
h the observation time. Our results indicated that GYLZ-RCC18 is an importa
nt novel gene related to renal cell carcinoma. Its overexpression would sti
mulate the growth and proliferation activity and plays an antidead and anti
apoptosis effect in renal cell carcinoma. Transfection of antisense oligonu
cleotide could inhibit the generation and development of renal cell carcino
ma. The study provides a new clue for the research of renal cell carcinoma,
and also provides an instruction for special genetic diagnosis and the the
rapy of renal cell carcinoma.