中国医师杂志
中國醫師雜誌
중국의사잡지
JOURNAL OF CHINESE PHYSICIAN
2009年
10期
1304-1307
,共4页
阳丽%刘惠宁%胡惠%李燕%方立%全细云
暘麗%劉惠寧%鬍惠%李燕%方立%全細雲
양려%류혜저%호혜%리연%방립%전세운
转录因子/代谢%绒毛膜癌/代谢%信号传导%肿瘤侵润%肿瘤转移
轉錄因子/代謝%絨毛膜癌/代謝%信號傳導%腫瘤侵潤%腫瘤轉移
전록인자/대사%융모막암/대사%신호전도%종류침윤%종류전이
Transcription factors/ME%Choriocarcioma/ME%Signal transduction%Neoplasm invasiveness%Neoplasm metastasis
目的 初步探讨信号转导与转录活化因子3(Stat3)与绒癌细胞侵袭转移能力的关系.方法 体外培养人绒毛膜癌细胞系JAR(低侵袭),JEG-3(高侵袭)及收集人正常早孕绒毛组织;运用Transwell体外侵袭实验检测并比较JAR和JEG-3细胞的侵袭转移潜能;采用Western-blot检测JAR、JEG-3细胞以及人正常早孕绒毛组织stat3及其活性形式P-star3蛋白的表达情况;同时用免疫组织细胞化学检测JAR和JEG-3细胞stat3及postat3蛋白的表达情况.结果 在人绒毛膜癌细胞中检测到stat3,p-star3的高表达;JEG-3细胞侵袭至基质胶膜背面的数量较JAR细胞明显增多(P<0.05);stat3及p-star3蛋白在绒癌细胞的表达强于正常绒毛组织(P<0.01),并且JEG-3细胞较JAR细胞显著增强(P<0.05).结论 stat3及p-star3在绒癌细胞中较正常绒毛组织高表达,且在JEG-3细胞的表达高于JAR细胞.
目的 初步探討信號轉導與轉錄活化因子3(Stat3)與絨癌細胞侵襲轉移能力的關繫.方法 體外培養人絨毛膜癌細胞繫JAR(低侵襲),JEG-3(高侵襲)及收集人正常早孕絨毛組織;運用Transwell體外侵襲實驗檢測併比較JAR和JEG-3細胞的侵襲轉移潛能;採用Western-blot檢測JAR、JEG-3細胞以及人正常早孕絨毛組織stat3及其活性形式P-star3蛋白的錶達情況;同時用免疫組織細胞化學檢測JAR和JEG-3細胞stat3及postat3蛋白的錶達情況.結果 在人絨毛膜癌細胞中檢測到stat3,p-star3的高錶達;JEG-3細胞侵襲至基質膠膜揹麵的數量較JAR細胞明顯增多(P<0.05);stat3及p-star3蛋白在絨癌細胞的錶達彊于正常絨毛組織(P<0.01),併且JEG-3細胞較JAR細胞顯著增彊(P<0.05).結論 stat3及p-star3在絨癌細胞中較正常絨毛組織高錶達,且在JEG-3細胞的錶達高于JAR細胞.
목적 초보탐토신호전도여전록활화인자3(Stat3)여융암세포침습전이능력적관계.방법 체외배양인융모막암세포계JAR(저침습),JEG-3(고침습)급수집인정상조잉융모조직;운용Transwell체외침습실험검측병비교JAR화JEG-3세포적침습전이잠능;채용Western-blot검측JAR、JEG-3세포이급인정상조잉융모조직stat3급기활성형식P-star3단백적표체정황;동시용면역조직세포화학검측JAR화JEG-3세포stat3급postat3단백적표체정황.결과 재인융모막암세포중검측도stat3,p-star3적고표체;JEG-3세포침습지기질효막배면적수량교JAR세포명현증다(P<0.05);stat3급p-star3단백재융암세포적표체강우정상융모조직(P<0.01),병차JEG-3세포교JAR세포현저증강(P<0.05).결론 stat3급p-star3재융암세포중교정상융모조직고표체,차재JEG-3세포적표체고우JAR세포.
Objective To explore the relationship between the expression of signal transducers and activators of transcription 3 (stat3),the invasiveness and metastasis mechanism of choriocarcinoma cells.Method Choriocarcinoma cell lines(JEG-3 cells and JAR cell)were cultured in vitro,and the human chorionic villi tissues were collected.The invasiveness was assessed by penetration through a matrigel-coated filter in transwell chamber ability between JEG-3 cells and JAR cell.Expression of star3 and p-star3 protein in the human chorionic villi tissues and choriocarcinoma cell lines(JEG-3 cells and JAR ceils)were detected by western blot and immunocytochemistry.Result The expression of stat3 and p-stat3 protein can be found in choriocarcinoma cell lines.The amount of JEG-3 cells penetrating through matrigel-coated filter in transweil chamber was significantly increased,compared with JAR cells(P<0.05).Protein expression level of star3 and p-star3 was significantly increased in JEG-3 cell line,compared with JAR cell line,and it was markedly increased in choriocarcinoma cell lines compared with normal villi tissues(P<0.01).SP immunocytocbemical results also showed that the expression of star3 and p-star3 was significantly increased in JEG-3 cell line,compared with JAR cell line(P<0.05).Conclusions The expression of stat3 and p-star3 protein in choriocarcinonm cells Was higher than that in normal villi tissues,and which in JEG-3 cells Was higher than that in JAR cells.