医药导报
醫藥導報
의약도보
HERALD OF MEDICINE
2015年
4期
455-458
,共4页
姜建武%李小兰%冷彦%陶德定%胡俊波%龚建平
薑建武%李小蘭%冷彥%陶德定%鬍俊波%龔建平
강건무%리소란%랭언%도덕정%호준파%공건평
槐耳颗粒%癌,结直肠%细胞,SW480%上皮-间质转化%侵袭%转移
槐耳顆粒%癌,結直腸%細胞,SW480%上皮-間質轉化%侵襲%轉移
괴이과립%암,결직장%세포,SW480%상피-간질전화%침습%전이
Huaier granules%Cancer,colorectal%Cell,SW480%Epithelial-mesenchymal transition%Invasion%Metastasis
目的:观察槐耳颗粒在体外对结肠癌SW480细胞侵袭转移的影响,并初步探讨其机制。方法 SubG1法确定槐耳颗粒促进结肠癌SW480细胞凋亡的最佳作用浓度和时间,通过划痕愈合实验和Transwell侵袭实验观察槐耳颗粒对结肠癌SW480细胞侵袭转移的影响。 Western blot法和 Real-Time PCR (荧光定量 PCR )法检测 E-cadherin、twist、snail、vimentin在蛋白和mRNA水平的变化。结果槐耳颗粒3.0 g·L-1处理SW480细胞36 h后凋亡最明显。槐耳颗粒3.0 g·L-1处理SW480细胞36 h后,划痕愈合实验相对迁移率为(31.36±2.39)%,而对照组36 h后相对迁移率则为(61.11±1.09)%(P<0.01)。 Transwell侵袭实验证实槐耳颗粒3.0 g·L-1处理SW480细胞36 h后每个视野穿透细胞数为(129±12)个,而对照组为(354±20)个(P<0.01)。槐耳颗粒3.0 g·L-1处理SW480细胞36 h后E-cadherin 在蛋白和mRNA水平表达均升高,而twist、snail和vimentin表达均降低。结论槐耳颗粒在体外能够通过抑制上皮-间质转化有效抑制结肠癌SW480细胞的侵袭转移。
目的:觀察槐耳顆粒在體外對結腸癌SW480細胞侵襲轉移的影響,併初步探討其機製。方法 SubG1法確定槐耳顆粒促進結腸癌SW480細胞凋亡的最佳作用濃度和時間,通過劃痕愈閤實驗和Transwell侵襲實驗觀察槐耳顆粒對結腸癌SW480細胞侵襲轉移的影響。 Western blot法和 Real-Time PCR (熒光定量 PCR )法檢測 E-cadherin、twist、snail、vimentin在蛋白和mRNA水平的變化。結果槐耳顆粒3.0 g·L-1處理SW480細胞36 h後凋亡最明顯。槐耳顆粒3.0 g·L-1處理SW480細胞36 h後,劃痕愈閤實驗相對遷移率為(31.36±2.39)%,而對照組36 h後相對遷移率則為(61.11±1.09)%(P<0.01)。 Transwell侵襲實驗證實槐耳顆粒3.0 g·L-1處理SW480細胞36 h後每箇視野穿透細胞數為(129±12)箇,而對照組為(354±20)箇(P<0.01)。槐耳顆粒3.0 g·L-1處理SW480細胞36 h後E-cadherin 在蛋白和mRNA水平錶達均升高,而twist、snail和vimentin錶達均降低。結論槐耳顆粒在體外能夠通過抑製上皮-間質轉化有效抑製結腸癌SW480細胞的侵襲轉移。
목적:관찰괴이과립재체외대결장암SW480세포침습전이적영향,병초보탐토기궤제。방법 SubG1법학정괴이과립촉진결장암SW480세포조망적최가작용농도화시간,통과화흔유합실험화Transwell침습실험관찰괴이과립대결장암SW480세포침습전이적영향。 Western blot법화 Real-Time PCR (형광정량 PCR )법검측 E-cadherin、twist、snail、vimentin재단백화mRNA수평적변화。결과괴이과립3.0 g·L-1처리SW480세포36 h후조망최명현。괴이과립3.0 g·L-1처리SW480세포36 h후,화흔유합실험상대천이솔위(31.36±2.39)%,이대조조36 h후상대천이솔칙위(61.11±1.09)%(P<0.01)。 Transwell침습실험증실괴이과립3.0 g·L-1처리SW480세포36 h후매개시야천투세포수위(129±12)개,이대조조위(354±20)개(P<0.01)。괴이과립3.0 g·L-1처리SW480세포36 h후E-cadherin 재단백화mRNA수평표체균승고,이twist、snail화vimentin표체균강저。결론괴이과립재체외능구통과억제상피-간질전화유효억제결장암SW480세포적침습전이。
Objective To investigate the effects of huaier granules on invasion and metastasis of colorectal cancer SW480 cells in vitro, and explore the basic mechanism. Methods The appropriate concentration and duration of huaier granules promoting SW480 cell apoptosis were determined by SubG1 method. Wound healing assay and transwell assay were used to observe the effect of huaier granules on SW480 cell invasion and metastasis. The changes of E-cadherin, twist, snail and vimentin at protein and mRNA levels were examined by Western blotting and Real-Time PCR. Results After treatment with huaier granules at 3. 0 g·L-1 for 36 h, apoptosis of SW480 cells was most significant, and wound healing assay revealed that relative mobility was (31. 36±2. 39)%, compared with (61. 11±1. 09)% in control group (P<0. 01). Number of invaded cells per field of view was (129±12) in treatment group and (354±20) in control group (P<0. 01). After treatment with huaier granules at 3. 0 g·L-1 for 36 h, protein and mRNA levels of E-cadherin were increased, while those of twist, snail and vimentin were decreased. Conclusion Huaier granules can inhibit invasion and metastasis of colorectal cancer SW480 cells in vitro through effectively depressing epithelial-mesenchymal transition.