实用癌症杂志
實用癌癥雜誌
실용암증잡지
The Practical Journal of Cancer
2015年
10期
1430-1433
,共4页
宋荣峰%张慧卿%熊彦%王艳华%万以叶
宋榮峰%張慧卿%熊彥%王豔華%萬以葉
송영봉%장혜경%웅언%왕염화%만이협
胃癌%5-FU%HSP27
胃癌%5-FU%HSP27
위암%5-FU%HSP27
Gastric cancer%5-FU%HSP27
目的:探讨热休克蛋白27(HSP27)在调控人胃癌细胞系5-FU耐药中的作用机制。方法培养人胃癌细胞株HGC27、BGC823、SGC7901、MKN28,采用CCK法筛选5-FU敏感株和耐药株,采用流式细胞仪和western blot 检测4株胃癌细胞株中HSP27表达水平,转染HSP27-siRNA,观察siRNA干扰后5-FU敏感株和耐药株中HSP27蛋白表达,并将两细胞株分别与不同浓度5-Fu共培养,采用CCK法检测细胞的半数抑制浓度( IC50)。结果 CCK法显示SGC7901细胞系是4株胃癌细胞中5-Fu相对耐药株,而HCG27是5-Fu相对敏感株。流式细胞仪显示SGC7901细胞株中HSP27表达水平最高为(72.10±1.89)%,而在HGC27细胞株中的表达水平最低为(22.12±1.33)%,各株表达水平比较差异有统计学意义( P<0.05)。转染HSP27-siRNA 后,各两株细胞HSP27蛋白表达水平均下降明显。与5-Fu共培养后, SGC7901细胞株转染组细胞半数抑制浓度降低,药物敏感性增强,与未转染组比较差异有统计学意义( P<0.05)。结论HSP27参与了SGC79015-FU耐药株中的细胞耐药,是诱导细胞多药耐药的重要分子机制,可以作为临床治疗靶点来提高胃癌患者对化疗的敏感性。
目的:探討熱休剋蛋白27(HSP27)在調控人胃癌細胞繫5-FU耐藥中的作用機製。方法培養人胃癌細胞株HGC27、BGC823、SGC7901、MKN28,採用CCK法篩選5-FU敏感株和耐藥株,採用流式細胞儀和western blot 檢測4株胃癌細胞株中HSP27錶達水平,轉染HSP27-siRNA,觀察siRNA榦擾後5-FU敏感株和耐藥株中HSP27蛋白錶達,併將兩細胞株分彆與不同濃度5-Fu共培養,採用CCK法檢測細胞的半數抑製濃度( IC50)。結果 CCK法顯示SGC7901細胞繫是4株胃癌細胞中5-Fu相對耐藥株,而HCG27是5-Fu相對敏感株。流式細胞儀顯示SGC7901細胞株中HSP27錶達水平最高為(72.10±1.89)%,而在HGC27細胞株中的錶達水平最低為(22.12±1.33)%,各株錶達水平比較差異有統計學意義( P<0.05)。轉染HSP27-siRNA 後,各兩株細胞HSP27蛋白錶達水平均下降明顯。與5-Fu共培養後, SGC7901細胞株轉染組細胞半數抑製濃度降低,藥物敏感性增彊,與未轉染組比較差異有統計學意義( P<0.05)。結論HSP27參與瞭SGC79015-FU耐藥株中的細胞耐藥,是誘導細胞多藥耐藥的重要分子機製,可以作為臨床治療靶點來提高胃癌患者對化療的敏感性。
목적:탐토열휴극단백27(HSP27)재조공인위암세포계5-FU내약중적작용궤제。방법배양인위암세포주HGC27、BGC823、SGC7901、MKN28,채용CCK법사선5-FU민감주화내약주,채용류식세포의화western blot 검측4주위암세포주중HSP27표체수평,전염HSP27-siRNA,관찰siRNA간우후5-FU민감주화내약주중HSP27단백표체,병장량세포주분별여불동농도5-Fu공배양,채용CCK법검측세포적반수억제농도( IC50)。결과 CCK법현시SGC7901세포계시4주위암세포중5-Fu상대내약주,이HCG27시5-Fu상대민감주。류식세포의현시SGC7901세포주중HSP27표체수평최고위(72.10±1.89)%,이재HGC27세포주중적표체수평최저위(22.12±1.33)%,각주표체수평비교차이유통계학의의( P<0.05)。전염HSP27-siRNA 후,각량주세포HSP27단백표체수평균하강명현。여5-Fu공배양후, SGC7901세포주전염조세포반수억제농도강저,약물민감성증강,여미전염조비교차이유통계학의의( P<0.05)。결론HSP27삼여료SGC79015-FU내약주중적세포내약,시유도세포다약내약적중요분자궤제,가이작위림상치료파점래제고위암환자대화료적민감성。
Objective To investigate the mechanism of HSP 27 of 5-FU resistant in human gastric cancer cell lines . Methods Human gastric cancer cell lines(HGC27,BGC823,SGC7901,MKN28)were cultured,and the cells which were resist-ant to 5-FU were selected by CCK assay and flow cytometry .The expression of HSP27 in these cells were detected by Western Blotting.And 2 cell lines were co-cultured with different concentration of 5-Fu,then the half inhibition concentration was detected by CCK assay.Results CCK assay showed that SGC7901 cell line was relatively resistant to 5-Fu,and the HCG27 cell line was relatively sensitive to 5-Fu.The flow cytometry results suggested that the expression of HSP 27 in the SGC7901 cells was the high-est(72.10 ±1.89)%.Nevertheless,it was the lowest in the HGC27 cells(22.12 ±1.33)%.After transfection by HSP27-siR-NA,the expression levels of HSP27 in two cell lines was significant decreased (P<0.05);however,co-cultured with 5-Fu,the half inhibition concentration of SGC 7901 cell lines was decreased ,meanwhile the sensitivity to 5-Fu was enhanced .Conclusion HSP27 is involved in the 5-Fu resistance of SGC7901 cells,it induced an important molecular mechanism of multi-drug resistance and could be applied as a therapeutic target in order to increase the sensitivity of chemotherapy .