实用癌症杂志
實用癌癥雜誌
실용암증잡지
THE PRACTICAL JOURNAL OF CANCER
2014年
4期
372-374
,共3页
金丹%吴明勇%刘建刚%袁淑芬%陈晓品
金丹%吳明勇%劉建剛%袁淑芬%陳曉品
금단%오명용%류건강%원숙분%진효품
TRPC1-SiRNA基因%肺腺癌A549细胞%增殖和侵袭
TRPC1-SiRNA基因%肺腺癌A549細胞%增殖和侵襲
TRPC1-SiRNA기인%폐선암A549세포%증식화침습
TRPC1-SiRNA gene%Lung Adenocarcinoma A 549 Cells%Cell Proliferation and Invasion
目的:观察SiRNA沉默TRPC1基因对肺腺癌A549细胞增殖和侵袭的影响效果。方法 TRPC1-SiRNA基因用特殊物质标记后,找出最适宜的转染浓度和时间,按照最适宜浓度和时间,培养空白对照组和转染试剂对照组,采用MTT法检测实验组、空白对照组以及转染试剂对照组的A549细胞增殖时间,通过侵袭实验观察3组A549细胞的侵袭能力。结果 TRPC1-SiRNA基因转染A549细胞48 h和100 mmol/L浓度下转染速率最快,因此两个对照组的时间和浓度也设定为48 h和100 mmol/L。 TRPC1-SiRNA基因转染A549细胞增殖时间明显短于未转染组和转染试剂对照组,差异均具有统计学意义(P<0.05)。 TRPC1-SiRNA基因转染A549细胞侵袭实验中穿膜细胞数实验组明显少于未转染组和转染试剂对照组,差异均具有统计学意义( P<0.05)。结论 SiRNA沉默TRPC1基因可抑制A549细胞的增殖,降低A549细胞的侵袭能力。
目的:觀察SiRNA沉默TRPC1基因對肺腺癌A549細胞增殖和侵襲的影響效果。方法 TRPC1-SiRNA基因用特殊物質標記後,找齣最適宜的轉染濃度和時間,按照最適宜濃度和時間,培養空白對照組和轉染試劑對照組,採用MTT法檢測實驗組、空白對照組以及轉染試劑對照組的A549細胞增殖時間,通過侵襲實驗觀察3組A549細胞的侵襲能力。結果 TRPC1-SiRNA基因轉染A549細胞48 h和100 mmol/L濃度下轉染速率最快,因此兩箇對照組的時間和濃度也設定為48 h和100 mmol/L。 TRPC1-SiRNA基因轉染A549細胞增殖時間明顯短于未轉染組和轉染試劑對照組,差異均具有統計學意義(P<0.05)。 TRPC1-SiRNA基因轉染A549細胞侵襲實驗中穿膜細胞數實驗組明顯少于未轉染組和轉染試劑對照組,差異均具有統計學意義( P<0.05)。結論 SiRNA沉默TRPC1基因可抑製A549細胞的增殖,降低A549細胞的侵襲能力。
목적:관찰SiRNA침묵TRPC1기인대폐선암A549세포증식화침습적영향효과。방법 TRPC1-SiRNA기인용특수물질표기후,조출최괄의적전염농도화시간,안조최괄의농도화시간,배양공백대조조화전염시제대조조,채용MTT법검측실험조、공백대조조이급전염시제대조조적A549세포증식시간,통과침습실험관찰3조A549세포적침습능력。결과 TRPC1-SiRNA기인전염A549세포48 h화100 mmol/L농도하전염속솔최쾌,인차량개대조조적시간화농도야설정위48 h화100 mmol/L。 TRPC1-SiRNA기인전염A549세포증식시간명현단우미전염조화전염시제대조조,차이균구유통계학의의(P<0.05)。 TRPC1-SiRNA기인전염A549세포침습실험중천막세포수실험조명현소우미전염조화전염시제대조조,차이균구유통계학의의( P<0.05)。결론 SiRNA침묵TRPC1기인가억제A549세포적증식,강저A549세포적침습능력。
Objective To observe the effect of silence TRPC 1 genes in SiRNA on proliferation and invasion of lung ade-nocarcinoma A549 cell.Methods TRPC1-SiRNA genes were marked with special materials , the most appropriate transfection concentration and time was identified ,and then the blank control group and transfection reagent control group were cultivated ac -cording to the most appropriate concentration and time .Through MTT tests and invasion tests ,cell proliferation and invasion ability of the experimental observation group ,the blank control group and the transfection reagent A 549 control group were observed and compared.Results The transfection of TRPC1-SiRNA for A549 cells had the highest concentration at 48 h and 100 mmol/L,so the time and concentration of the other 2 control groups were set at 48 h and 100 mmol/L for concentration .The proliferation time of the TRPC1-SiRNA gene transfection for A549 cell was significantly less than that of non-transfection group and transfection rea-gent control group,there had statistical difference (P<0.05).The septum-permeating cells of the TRPC1-SiRNA gene transfec-tion for A549 cell in the invasive experiments was significantly less than that of non-transfection group and transfection reagent control group,there had statistical differences (P<0.05).Conclusion SiRNA silence TRPC1 genes can inhibit the proliferation of A549 cells and reduce the invasive ability of A 549 cells.