郑州大学学报(医学版)
鄭州大學學報(醫學版)
정주대학학보(의학판)
JOURNAL OF ZHENGZHOU UNIVERSITY(MEDICAL SCIENCES)
2014年
2期
146-149
,共4页
张岚%高冬玲%温洪涛%张蕾
張嵐%高鼕玲%溫洪濤%張蕾
장람%고동령%온홍도%장뢰
食管癌%凋亡%Bcl-XL%反义寡核苷酸%EC9706细胞%裸鼠
食管癌%凋亡%Bcl-XL%反義寡覈苷痠%EC9706細胞%裸鼠
식관암%조망%Bcl-XL%반의과핵감산%EC9706세포%라서
esophageal cancer%apoptosis%Bcl-XL%antisense oligodeoxynucleotide%EC9706 cell%nude mouse
目的:探讨Bcl-XL反义寡核苷酸( Bcl-XL ASODN)对食管癌EC9706细胞和人食管癌裸鼠移植瘤组织的诱凋亡作用。方法:将合成的Bcl-XL ASODN通过阳离子脂质体介导转染EC9706细胞后,以吖啶橙荧光染色、流式细胞术和TUNEL技术检测ASODN组、细胞对照组、空白对照组和N-ODN组的凋亡率;用TUNEL技术检测ASODN组、N-ODN组和细胞对照组裸鼠移植瘤组织的细胞凋亡率。结果:吖啶橙荧光染色、流式细胞术和TUNEL检测结果显示,ASODN组、N-ODN组、空白对照组和细胞对照组的凋亡率比较,差异均有统计学意义(F=26.853、38.537、28.541,P均<0.001);且ASODN组的凋亡率均高于细胞对照组、空白对照组和N-ODN组(P均<0.05);TUNEL法检测移植瘤组织的细胞凋亡率结果显示,细胞对照组、N-ODN组及ASODN组的凋亡率比较,差异有统计学意义(F=56.375,P<0.001);且ASODN组高于细胞对照组及N-ODN组(P均<0.05)。结论:Bcl-XL ASODN对食管癌EC9706细胞及食管癌裸鼠移植瘤组织均有诱凋亡作用。
目的:探討Bcl-XL反義寡覈苷痠( Bcl-XL ASODN)對食管癌EC9706細胞和人食管癌裸鼠移植瘤組織的誘凋亡作用。方法:將閤成的Bcl-XL ASODN通過暘離子脂質體介導轉染EC9706細胞後,以吖啶橙熒光染色、流式細胞術和TUNEL技術檢測ASODN組、細胞對照組、空白對照組和N-ODN組的凋亡率;用TUNEL技術檢測ASODN組、N-ODN組和細胞對照組裸鼠移植瘤組織的細胞凋亡率。結果:吖啶橙熒光染色、流式細胞術和TUNEL檢測結果顯示,ASODN組、N-ODN組、空白對照組和細胞對照組的凋亡率比較,差異均有統計學意義(F=26.853、38.537、28.541,P均<0.001);且ASODN組的凋亡率均高于細胞對照組、空白對照組和N-ODN組(P均<0.05);TUNEL法檢測移植瘤組織的細胞凋亡率結果顯示,細胞對照組、N-ODN組及ASODN組的凋亡率比較,差異有統計學意義(F=56.375,P<0.001);且ASODN組高于細胞對照組及N-ODN組(P均<0.05)。結論:Bcl-XL ASODN對食管癌EC9706細胞及食管癌裸鼠移植瘤組織均有誘凋亡作用。
목적:탐토Bcl-XL반의과핵감산( Bcl-XL ASODN)대식관암EC9706세포화인식관암라서이식류조직적유조망작용。방법:장합성적Bcl-XL ASODN통과양리자지질체개도전염EC9706세포후,이아정등형광염색、류식세포술화TUNEL기술검측ASODN조、세포대조조、공백대조조화N-ODN조적조망솔;용TUNEL기술검측ASODN조、N-ODN조화세포대조조라서이식류조직적세포조망솔。결과:아정등형광염색、류식세포술화TUNEL검측결과현시,ASODN조、N-ODN조、공백대조조화세포대조조적조망솔비교,차이균유통계학의의(F=26.853、38.537、28.541,P균<0.001);차ASODN조적조망솔균고우세포대조조、공백대조조화N-ODN조(P균<0.05);TUNEL법검측이식류조직적세포조망솔결과현시,세포대조조、N-ODN조급ASODN조적조망솔비교,차이유통계학의의(F=56.375,P<0.001);차ASODN조고우세포대조조급N-ODN조(P균<0.05)。결론:Bcl-XL ASODN대식관암EC9706세포급식관암라서이식류조직균유유조망작용。
Aim:To investigate the effects of inducing apoptosis on esophageal cancer EC 9706 cells and xenograft tis-sue of human esophageal cancer in nude mice treated by Bcl-XL antisense oligodeoxynucleotide ( ASODN) .Methods:Bcl-XL ASODN was transfected into EC9706 cells following cationic liposome(ASODN group).N-ODN group, the cell control group and the blank control group were the control .The apoptosis rate of each cell groups was detected by acridine orange ( AO) fluorescent staining , flow cytometry and TUNEL , respectively .The apoptosis rate in xenograft tissue from nude mice in ASODN group, N-ODN group and the cell control group was detected by TUNEL .Resul ts:The results of AO fluores-cent staining, flow cytometry and TUNEL showed that there were significant differences in apoptosis rates among ASODN group,the cell control group, the blank control group and N-ODN group(F=26.853,38.537, 28.541,P<0.001).The ap-optosis rate was higher in ASODN group compared with the cell control ,the blank control and NO-DN groups(P<0.05). The apoptosis rates in xenograft tissue detected by TUNEL showed that there were significant differences among ASODN group, the cell control group and N-ODN group(F =563.75, P<0.001).The apoptosis rate was higher in ASODN group compared with the cell control group and N-ODN group(P<0.05).Conclusion:Bcl-XL ASODN could effectively induce apoptosis of EC9706 cell and xenograft tissue of human esophageal carcinoma .