生物技术通报
生物技術通報
생물기술통보
BIOTECHNOLOGY BULLETIN
2010年
1期
157-161
,共5页
杨淑哲%罗春丽%吴小候%潘翠翠%荀春华%蒲军
楊淑哲%囉春麗%吳小候%潘翠翠%荀春華%蒲軍
양숙철%라춘려%오소후%반취취%순춘화%포군
肾透明细胞癌%hepaCAM%VEGF%侵袭转移
腎透明細胞癌%hepaCAM%VEGF%侵襲轉移
신투명세포암%hepaCAM%VEGF%침습전이
Renal cell carcinomas%hepaCAM%VEGF%Invasion and metastasis
研究肾癌细胞株786- 0,RC- 2及肾透明细胞癌组织中肝细胞黏附分子(hepatocyte cell adhesion molecule,hepaCAM)和血管内皮生长因子(VEGF)mRNA表达及其与肾透明细胞癌侵袭转移的关系.应用逆转录聚合酶链反应(RT-PCR)检测786- 0、RC- 2、正常肾组织hepaCAM和VEGF mRNA表达,73例肾透明细胞癌组织及相应癌旁组织中hepaCAM mRNA表达,43例肾透明细胞癌组织及相应癌旁组织VEGF mRNA表达,并比较它们之间的差异性和相关性.与正常肾组织比较786- 0,RC- 2的hepaCAM mRNA显著降低(P<0.05);VEGF mRNA显著升高(P<0.05).肾透明细胞癌组织hepaCAM mRNA显著低于癌旁组织(P<0.05);VEGF mRNA显著高于癌旁组织(P<0.05).在肾透明细胞癌组织中临床Ⅰ+Ⅱ期和Ⅲ+Ⅳ期两组VEGF mRNA表达差异具有统计学意义(P<0.05),hepaCAM与VEGF mRNA呈负相关(r=-0.329,P<0.05).提示hepaCAM基因缺失可能参与肾透明细胞癌侵袭转移,其机制可能与调节VFGF表达改变有关,hepaCAM有望成为一种新的肾癌基因治疗的靶分子.
研究腎癌細胞株786- 0,RC- 2及腎透明細胞癌組織中肝細胞黏附分子(hepatocyte cell adhesion molecule,hepaCAM)和血管內皮生長因子(VEGF)mRNA錶達及其與腎透明細胞癌侵襲轉移的關繫.應用逆轉錄聚閤酶鏈反應(RT-PCR)檢測786- 0、RC- 2、正常腎組織hepaCAM和VEGF mRNA錶達,73例腎透明細胞癌組織及相應癌徬組織中hepaCAM mRNA錶達,43例腎透明細胞癌組織及相應癌徬組織VEGF mRNA錶達,併比較它們之間的差異性和相關性.與正常腎組織比較786- 0,RC- 2的hepaCAM mRNA顯著降低(P<0.05);VEGF mRNA顯著升高(P<0.05).腎透明細胞癌組織hepaCAM mRNA顯著低于癌徬組織(P<0.05);VEGF mRNA顯著高于癌徬組織(P<0.05).在腎透明細胞癌組織中臨床Ⅰ+Ⅱ期和Ⅲ+Ⅳ期兩組VEGF mRNA錶達差異具有統計學意義(P<0.05),hepaCAM與VEGF mRNA呈負相關(r=-0.329,P<0.05).提示hepaCAM基因缺失可能參與腎透明細胞癌侵襲轉移,其機製可能與調節VFGF錶達改變有關,hepaCAM有望成為一種新的腎癌基因治療的靶分子.
연구신암세포주786- 0,RC- 2급신투명세포암조직중간세포점부분자(hepatocyte cell adhesion molecule,hepaCAM)화혈관내피생장인자(VEGF)mRNA표체급기여신투명세포암침습전이적관계.응용역전록취합매련반응(RT-PCR)검측786- 0、RC- 2、정상신조직hepaCAM화VEGF mRNA표체,73례신투명세포암조직급상응암방조직중hepaCAM mRNA표체,43례신투명세포암조직급상응암방조직VEGF mRNA표체,병비교타문지간적차이성화상관성.여정상신조직비교786- 0,RC- 2적hepaCAM mRNA현저강저(P<0.05);VEGF mRNA현저승고(P<0.05).신투명세포암조직hepaCAM mRNA현저저우암방조직(P<0.05);VEGF mRNA현저고우암방조직(P<0.05).재신투명세포암조직중림상Ⅰ+Ⅱ기화Ⅲ+Ⅳ기량조VEGF mRNA표체차이구유통계학의의(P<0.05),hepaCAM여VEGF mRNA정부상관(r=-0.329,P<0.05).제시hepaCAM기인결실가능삼여신투명세포암침습전이,기궤제가능여조절VFGF표체개변유관,hepaCAM유망성위일충신적신암기인치료적파분자.
It was to investigate the expression of hepaCAM and VEGF mRNA in renal cancer cells 786- 0,RC- 2 ,renal cell carcinomas(RCC)and their relation to invasion and metastasis of renal cell carcinomas(RCC).The expression of hepaCAM and VEGF mRNA was determined in 786- 0,RC- 2,normal renal tissue,the expression of hepaCAM mRNA was determined in 73 cases of RCC and corresponding peripheral noncancerous tissue and the expression of VEGF mRNA was determined in 43 cases of RCC and corresponding peripheral noncancerous tissue by reverse transcription polymerase chain reaction(RT-PCR).The difference and corelation between each group were compared and analyzed.Results indicate that hepaCAM mRNA′s expression was lower in 786- 0,RC- 2 than in the normal tissue(P<0.05),VEGF mRNA′s expression was higher in 786- 0,RC- 2 than that of in the normal tissue(P<0.05).In RCC tissues hepaCAM mRNA′s expression was significantly lower than corresponding peripheral noncancerous tissues(P<0.05),VEGF mRNA′s expression was significantly higher than corresponding peripheral noncancerous tissues.There are significance between stage Ⅰ+Ⅱgroup and stageⅢ+Ⅳ group as far as VEGF mRNA expression are concerned(P<0.05)and hepaCAM mRNA expression level was negatively correlated with the VEGF mRNA in RCC(r =-0.329,P<0.05).Therefore,the down regulation of hepaCAM contributes to the invasiveness and metastasis of RCC,and the mechanism may be associated with the change of VEGF expression.hepaCAM is expected to become a new molecular in the gene therapy of RCC.