浙江临床医学
浙江臨床醫學
절강림상의학
Zhejiang Clinical Medical Journal
2015年
9期
1457-1459
,共3页
何永礼%王欣%施福田%严秋亮%朱锦辉
何永禮%王訢%施福田%嚴鞦亮%硃錦輝
하영례%왕흔%시복전%엄추량%주금휘
Aurora-A激酶%胰腺癌%多药耐药%吉西他滨
Aurora-A激酶%胰腺癌%多藥耐藥%吉西他濱
Aurora-A격매%이선암%다약내약%길서타빈
Aurora-A kinase%Pancreatic carcinoma%Multiple drug resistance%Gemcitabine
目的:探讨Aurora-A的表达与胰腺癌吉西他滨耐药的相关性。方法 qPCR法测定PANC-1和耐药细胞株PANC-1/R2中Aurora-A mRNA的表达;分别用PANC-1和PANC-1/R2建立胰腺癌动物模型,免疫组化方法测定瘤体Aurora-A的表达。结果 PANC-1组模型第5周肿瘤转移率36.8%(7/19),裸鼠体重(23.2±1.41)g,肿瘤重量(0.453±0.110)g;PANC-1/R2组模型第5周肿瘤转移率50%(9/18),裸鼠体重(22.91±1.13)g,肿瘤重量(0.564±0.203)g。转移率和肿瘤质量两组比较差异有统计学意义。PANC-1组Aurora-A mRNA表达为(1.002±0.040);PANC-1/R2组Aurora-A mRNA表达为(1.845±0.069),两组比较差异有统计学意义(P<0.05)。PANC-1/R2组18例标本组织中Aurora-A蛋白阳性表达15例(83.3%);PANC-1组19例组织的Aurora-A蛋白检测阳性表达11例(57.9%),两组比较差异有统计学意义(P<0.05)。结论 Aurora-A基因高表达与胰腺癌细胞株的吉西他滨耐药有关,新方法构建的PANC-1/R2耐药株Aurora-A基因高表达,可用于胰腺癌吉西他滨耐药研究的载体。
目的:探討Aurora-A的錶達與胰腺癌吉西他濱耐藥的相關性。方法 qPCR法測定PANC-1和耐藥細胞株PANC-1/R2中Aurora-A mRNA的錶達;分彆用PANC-1和PANC-1/R2建立胰腺癌動物模型,免疫組化方法測定瘤體Aurora-A的錶達。結果 PANC-1組模型第5週腫瘤轉移率36.8%(7/19),裸鼠體重(23.2±1.41)g,腫瘤重量(0.453±0.110)g;PANC-1/R2組模型第5週腫瘤轉移率50%(9/18),裸鼠體重(22.91±1.13)g,腫瘤重量(0.564±0.203)g。轉移率和腫瘤質量兩組比較差異有統計學意義。PANC-1組Aurora-A mRNA錶達為(1.002±0.040);PANC-1/R2組Aurora-A mRNA錶達為(1.845±0.069),兩組比較差異有統計學意義(P<0.05)。PANC-1/R2組18例標本組織中Aurora-A蛋白暘性錶達15例(83.3%);PANC-1組19例組織的Aurora-A蛋白檢測暘性錶達11例(57.9%),兩組比較差異有統計學意義(P<0.05)。結論 Aurora-A基因高錶達與胰腺癌細胞株的吉西他濱耐藥有關,新方法構建的PANC-1/R2耐藥株Aurora-A基因高錶達,可用于胰腺癌吉西他濱耐藥研究的載體。
목적:탐토Aurora-A적표체여이선암길서타빈내약적상관성。방법 qPCR법측정PANC-1화내약세포주PANC-1/R2중Aurora-A mRNA적표체;분별용PANC-1화PANC-1/R2건립이선암동물모형,면역조화방법측정류체Aurora-A적표체。결과 PANC-1조모형제5주종류전이솔36.8%(7/19),라서체중(23.2±1.41)g,종류중량(0.453±0.110)g;PANC-1/R2조모형제5주종류전이솔50%(9/18),라서체중(22.91±1.13)g,종류중량(0.564±0.203)g。전이솔화종류질량량조비교차이유통계학의의。PANC-1조Aurora-A mRNA표체위(1.002±0.040);PANC-1/R2조Aurora-A mRNA표체위(1.845±0.069),량조비교차이유통계학의의(P<0.05)。PANC-1/R2조18례표본조직중Aurora-A단백양성표체15례(83.3%);PANC-1조19례조직적Aurora-A단백검측양성표체11례(57.9%),량조비교차이유통계학의의(P<0.05)。결론 Aurora-A기인고표체여이선암세포주적길서타빈내약유관,신방법구건적PANC-1/R2내약주Aurora-A기인고표체,가용우이선암길서타빈내약연구적재체。
ObjectiveTo assess the relationship of Aurora-A expression with gemcitabine-resistance of pancreatic cancer.MethodsThe expression of Aurora-A mRNA of PANC-1 and PANC-1/R2 cells were tested by qPCR technique. The animal models of pancreatic cancer were estblised by PANC-1 and PANC-1/R2 cells. After 35days,mice were killed,and the tumor tissues were collected. The Aurora-A protein expression of the two groups were deteched by Immunohistochemistry.ResultsIn the PANC-1 group,the metastasis of tumor on the five weeks was 36.8%(7/19), the mean weight of tumor tissues was 0.453±0.110 g,and weight of mice was 23.2±1.41 g. While the metastasis of tumor on the five weeks was 50%(9/18),the mean weight of tumor tissues was 0.564±0.203g,and weight of mice was 22.91±1.13g in PANC-1/R2 group. The metastatic rate and weight of tumor were with significant differences(P<0.05). The expression of Aurora-A mRNA of PANC-1 cells was 1.002±0.040;while it was 1.845±0.069 in PANC-1/R2,it was significant difference between the two groups(P<0.05). A 15 of 18 cases positive expression of Aurora-A protein were detected in PANC-1/R2 group,while it was 11 of 19 cases in PANC-1 group. The significant difference was found between the two groups (P<0.05).Conclusions High expression of Aurora-A gene is associated with gemcitabine- resistance of pancreatic cancer cell lines. PANC-1/R2 cell was successful as a cell model of gemcitabine-resistance of pancreatic cancer.