重庆医学
重慶醫學
중경의학
CHONGQING MEDICAL JOURNAL
2013年
25期
2983-2985
,共3页
张宇骄%刘玲%汪春燕%詹平%伍宗惠%何雯%王定玉
張宇驕%劉玲%汪春燕%詹平%伍宗惠%何雯%王定玉
장우교%류령%왕춘연%첨평%오종혜%하문%왕정옥
子宫内膜肿瘤%LRP16基因%HEC-1-B细胞
子宮內膜腫瘤%LRP16基因%HEC-1-B細胞
자궁내막종류%LRP16기인%HEC-1-B세포
endometrial carcinoma%LRP16 gene%HEC-1-B cells
目的:研究LRP16在子宫内膜癌组织中的表达变化及其对子宫内膜癌 HEC-1-B细胞增殖的影响。方法:应用逆转录聚合酶链反应(RT-PCR)检测26例正常子宫内膜组织及10例子宫内膜癌组织中LRP16 mRNA的表达;LRP16转染细胞, RT-PCR证实转染的成功性,WST-1法观察细胞增殖的变化。结果子宫内膜癌组织中LRP16 mRNA的阳性表达率及表达水平(分别为83.33%、0.82±0.21)明显高于正常子宫内膜组织(分别为30.00%、0.47±0.18),二者比较差异有统计学意义( P<0.05)。RT-PCR检测结果显示转染后细胞LRP16 mRNA表达明显增加。转染组 HEC-1-B细胞在体外能继续增殖,但增殖能力并没有增强。结论: LRP16的异常表达可能与子宫内膜癌的发生、发展密切相关,LRP16基因用于子宫内膜癌基因治疗可能具有潜在价值。
目的:研究LRP16在子宮內膜癌組織中的錶達變化及其對子宮內膜癌 HEC-1-B細胞增殖的影響。方法:應用逆轉錄聚閤酶鏈反應(RT-PCR)檢測26例正常子宮內膜組織及10例子宮內膜癌組織中LRP16 mRNA的錶達;LRP16轉染細胞, RT-PCR證實轉染的成功性,WST-1法觀察細胞增殖的變化。結果子宮內膜癌組織中LRP16 mRNA的暘性錶達率及錶達水平(分彆為83.33%、0.82±0.21)明顯高于正常子宮內膜組織(分彆為30.00%、0.47±0.18),二者比較差異有統計學意義( P<0.05)。RT-PCR檢測結果顯示轉染後細胞LRP16 mRNA錶達明顯增加。轉染組 HEC-1-B細胞在體外能繼續增殖,但增殖能力併沒有增彊。結論: LRP16的異常錶達可能與子宮內膜癌的髮生、髮展密切相關,LRP16基因用于子宮內膜癌基因治療可能具有潛在價值。
목적:연구LRP16재자궁내막암조직중적표체변화급기대자궁내막암 HEC-1-B세포증식적영향。방법:응용역전록취합매련반응(RT-PCR)검측26례정상자궁내막조직급10례자궁내막암조직중LRP16 mRNA적표체;LRP16전염세포, RT-PCR증실전염적성공성,WST-1법관찰세포증식적변화。결과자궁내막암조직중LRP16 mRNA적양성표체솔급표체수평(분별위83.33%、0.82±0.21)명현고우정상자궁내막조직(분별위30.00%、0.47±0.18),이자비교차이유통계학의의( P<0.05)。RT-PCR검측결과현시전염후세포LRP16 mRNA표체명현증가。전염조 HEC-1-B세포재체외능계속증식,단증식능력병몰유증강。결론: LRP16적이상표체가능여자궁내막암적발생、발전밀절상관,LRP16기인용우자궁내막암기인치료가능구유잠재개치。
Objective To investigate the expression change of LRP16 in endometrial cancer tissues and its influence on the pro-liferation of human endometrial carcinoma HEC-1-B cells .Methods HEC-1-B cells were transfected with LRP16 .RT-PCR was used to examine the expression of LRP16 in 26 normal endometrium specimens ,10 endometrial cancer specimens .RT-PCR was used for verifying the transfection success .WES-T was used to observe the proliferation change of HEC-1-B cells .Results The positive expression rate and level of LRP16 mRNA in the endometrial cancer tissues were 83 .33% and 0 .82 ± 0 .21 ,which were significantly higher than 30 .00% ,0 .47 ± 0 .18 in the normal endometrium tissues(P<0 .05) .The RT-PCR detection results revealed that the expression of LRP16 mRNA after transfection was significantly increased .HEC-1-B cells in the transfection group could continued to proliferate in vitro ,but the proliferation capacity was not increased .Conclusion The expression abnormality of LRP16 may be closely related to the occurrence and progress of endometrial cancer ,LRP16 gene may have potential value for the endometrial canc-er gene therapy .