中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2013年
6期
1110-1112,1327
,共4页
向威%赵军%刘周强%曾鹏%蒋国松%章小平%陈朝晖
嚮威%趙軍%劉週彊%曾鵬%蔣國鬆%章小平%陳朝暉
향위%조군%류주강%증붕%장국송%장소평%진조휘
肾透明细胞癌%基因表达%抑癌基因
腎透明細胞癌%基因錶達%抑癌基因
신투명세포암%기인표체%억암기인
Clear cell renal cell carcinoma%Gene expression%Tumor suppressor genes
目的 观察肾透明细胞癌(ccRCC)与正常肾组织中ALS2CL基因的表达及差异,并探讨其意义.方法 采用实时定量聚合酶链反应(Real-time PCR)、免疫组织化学(IPH)及Western blot检测26例配对癌组织/癌旁正常肾组织标本及2株ccRCC来源细胞(786/O、SN12-PM6)中ALS2CL基因mRNA和蛋白的表达.结果 与正常对照组比较,ALS2CL基因mRNA在65.38%(17/26)的ccRCC组织中表达显著下调,在786/O、SN12-PM6中表达亦显著下调;IPH结果示73.08%(19/26) ccRCC组织ALS2CL蛋白呈阴性或弱阳性表达;Western blot结果示53.58%(14/26) ccRCC组织ALS2CL蛋白表达下调,2株细胞ALS2CL蛋白表达亦下调,与各自对照组比较,其表达差异均有统计学意义(P<0.05).结论 ALS2CL基因表达缺失或下调可能与肾透明细胞癌发生密切相关.
目的 觀察腎透明細胞癌(ccRCC)與正常腎組織中ALS2CL基因的錶達及差異,併探討其意義.方法 採用實時定量聚閤酶鏈反應(Real-time PCR)、免疫組織化學(IPH)及Western blot檢測26例配對癌組織/癌徬正常腎組織標本及2株ccRCC來源細胞(786/O、SN12-PM6)中ALS2CL基因mRNA和蛋白的錶達.結果 與正常對照組比較,ALS2CL基因mRNA在65.38%(17/26)的ccRCC組織中錶達顯著下調,在786/O、SN12-PM6中錶達亦顯著下調;IPH結果示73.08%(19/26) ccRCC組織ALS2CL蛋白呈陰性或弱暘性錶達;Western blot結果示53.58%(14/26) ccRCC組織ALS2CL蛋白錶達下調,2株細胞ALS2CL蛋白錶達亦下調,與各自對照組比較,其錶達差異均有統計學意義(P<0.05).結論 ALS2CL基因錶達缺失或下調可能與腎透明細胞癌髮生密切相關.
목적 관찰신투명세포암(ccRCC)여정상신조직중ALS2CL기인적표체급차이,병탐토기의의.방법 채용실시정량취합매련반응(Real-time PCR)、면역조직화학(IPH)급Western blot검측26례배대암조직/암방정상신조직표본급2주ccRCC래원세포(786/O、SN12-PM6)중ALS2CL기인mRNA화단백적표체.결과 여정상대조조비교,ALS2CL기인mRNA재65.38%(17/26)적ccRCC조직중표체현저하조,재786/O、SN12-PM6중표체역현저하조;IPH결과시73.08%(19/26) ccRCC조직ALS2CL단백정음성혹약양성표체;Western blot결과시53.58%(14/26) ccRCC조직ALS2CL단백표체하조,2주세포ALS2CL단백표체역하조,여각자대조조비교,기표체차이균유통계학의의(P<0.05).결론 ALS2CL기인표체결실혹하조가능여신투명세포암발생밀절상관.
Objective To study the differential expression of ALS2CL in clear cell renal cell carcinoma (ccRCC) and normal kidney tissue and the implication.Methods Real-time quantitative polymerase chain reaction (Real-time PCR),immunohistochemistry (IPH) and Western blotting were applied to examine the expression status of ALS2CL in 26 ccRCC tumor and adjacent normal kidney tissue samples as well as two kinds of ccRCC-derived cell lines (786/O,SN12-PM6).Results As compared with normal control group,the two ccRCC-derived cell lines (786/O,SN12-PM6) and 65.38% (17/26) of ccRCC alls showed an obvious down-regulated expression of ALS2CL mRNA.Under the examination of ALS2CL protein by IPH,73.08% (19/26) of ccRCC specimens were negative or weakly positive.Western blotting also showed a highly down-regulated rate-53.85% (14/26) in ccRCC samples,and the low expression of ALS2CL was also found in 786/O and SN12-PM6 cells.All of them showed statistically significant difference between ccRCC group and corresponding normal control group (P < 0.05).Conclusion The absence or downregulated expression of ALS2CL may be closely related to the occurrence of ccRCC.