中华检验医学杂志
中華檢驗醫學雜誌
중화검험의학잡지
CHINESE JOURNAL OF LABORATORY MEDICINE
2009年
4期
455-458
,共4页
彭海霞%关明%陈宇明%陶琨%金云菲%李吉%王赛玉%钱爱华
彭海霞%關明%陳宇明%陶琨%金雲菲%李吉%王賽玉%錢愛華
팽해하%관명%진우명%도곤%금운비%리길%왕새옥%전애화
结肠肿瘤%RNA,小分子干扰%氟尿嘧啶%核蛋白质类%肿瘤抑制蛋白质类
結腸腫瘤%RNA,小分子榦擾%氟尿嘧啶%覈蛋白質類%腫瘤抑製蛋白質類
결장종류%RNA,소분자간우%불뇨밀정%핵단백질류%종류억제단백질류
Colonic neoplasms%RNA,small interfering%Fluomuracii%Nuclear proteins%Tumor suppressor proteins
目的 探讨小干扰RNA(siRNA)调节导致的△Np73抑制对结肠癌细胞SW620 5-氟尿嘧啶(5-FU)药物敏感性的影响,为结肠癌治疗提供新途径.方法 将△Np73 siRNA转染人SW620结肠癌细胞,观察其对结肠癌细胞△Np73表达的影响.并与5-FU联合使用,四甲基偶氮唑盐比色(MTT)法检测细胞活力,流式细胞技术检测细胞凋亡.分别将转染△Np73 siRNA和阴性对照siRNA的SW620细胞注射裸鼠成瘤,瘤中注射5-FU观察体内肿瘤的生长情况.结果 △Np73 siRNA可显著抑制SW620结肠癌细胞△Np73的表达,但本身均不能抑制SW620结肠癌细胞的生长.同时应用△Np73 siRNA和5-FU共同处理的SW620细胞的凋亡率达到42.9%,显著高于单纯5-FU处理组(18.9%)和单纯△Np73处理组(8.8%).在转染△Np73 siRNA的成瘤小鼠的瘤中注射5-FU,能明显抑制癌细胞体外生长(t=15.32,P<0.05).结论 △Np73 siRNA可通过抑制△Np73的表达,从而增强对化疗药物的敏感性.
目的 探討小榦擾RNA(siRNA)調節導緻的△Np73抑製對結腸癌細胞SW620 5-氟尿嘧啶(5-FU)藥物敏感性的影響,為結腸癌治療提供新途徑.方法 將△Np73 siRNA轉染人SW620結腸癌細胞,觀察其對結腸癌細胞△Np73錶達的影響.併與5-FU聯閤使用,四甲基偶氮唑鹽比色(MTT)法檢測細胞活力,流式細胞技術檢測細胞凋亡.分彆將轉染△Np73 siRNA和陰性對照siRNA的SW620細胞註射裸鼠成瘤,瘤中註射5-FU觀察體內腫瘤的生長情況.結果 △Np73 siRNA可顯著抑製SW620結腸癌細胞△Np73的錶達,但本身均不能抑製SW620結腸癌細胞的生長.同時應用△Np73 siRNA和5-FU共同處理的SW620細胞的凋亡率達到42.9%,顯著高于單純5-FU處理組(18.9%)和單純△Np73處理組(8.8%).在轉染△Np73 siRNA的成瘤小鼠的瘤中註射5-FU,能明顯抑製癌細胞體外生長(t=15.32,P<0.05).結論 △Np73 siRNA可通過抑製△Np73的錶達,從而增彊對化療藥物的敏感性.
목적 탐토소간우RNA(siRNA)조절도치적△Np73억제대결장암세포SW620 5-불뇨밀정(5-FU)약물민감성적영향,위결장암치료제공신도경.방법 장△Np73 siRNA전염인SW620결장암세포,관찰기대결장암세포△Np73표체적영향.병여5-FU연합사용,사갑기우담서염비색(MTT)법검측세포활력,류식세포기술검측세포조망.분별장전염△Np73 siRNA화음성대조siRNA적SW620세포주사라서성류,류중주사5-FU관찰체내종류적생장정황.결과 △Np73 siRNA가현저억제SW620결장암세포△Np73적표체,단본신균불능억제SW620결장암세포적생장.동시응용△Np73 siRNA화5-FU공동처리적SW620세포적조망솔체도42.9%,현저고우단순5-FU처리조(18.9%)화단순△Np73처리조(8.8%).재전염△Np73 siRNA적성류소서적류중주사5-FU,능명현억제암세포체외생장(t=15.32,P<0.05).결론 △Np73 siRNA가통과억제△Np73적표체,종이증강대화료약물적민감성.
Objective To investigate the effect of small interfering RNA (siRNA) mediated silencing of △Np73 on 5-FU chemotherapy sensitivity in SW620 colocancer cells and provide new treatment approach for the colon cancer.Methods siRNAs were transfected into SW620 colon cancer cells.The expression of △Np73 was observed.Cell viability of colon cancer cells were measured by MTr assay and cell apoptosis was assessed with flow cytometry after treatment of control siRNA or △Np73 siRNA or combined with 5-FU,respectively.The tumorigenesis was assessed by injecting △Np73 siRNA or control siRNA transfeeted SW620 colon cancer cells into nude mice,followed by treatment with 5-FU in the tumors.Results △Np73 siRNA was able to strongly inhibit △Np73 expression,however,it did not inhibit the growth of cells.Combination treatment with △Np73 siRNA and 5-FU produced significant higher apoptotic cell(42.9%) as compared with those with 5-FU treatment(18.9%) alone or those with △Np73 siRNA(8.8%) alone.The treatment with 5-FU in the xenngrafts derived from △Np73 siRNA transfected SW620 cells in nude mice can inhibitor tumor growth significantly (t=15.32,P<0.05).Conclusion △Np73siRNAs can specifically repress the expression of △Np73.Thus it sensitizess the cells to 5-FU chemotherapy in colon cancer.