浙江医学
浙江醫學
절강의학
ZHEJIANG MEDICAL JOURNAL
2013年
17期
1554-1556
,共3页
子宫内膜癌%ER- α基因多态性%易感性
子宮內膜癌%ER- α基因多態性%易感性
자궁내막암%ER- α기인다태성%역감성
Endometrial carcinoma%ER- αgene polymorphisms%Susceptibility
目的探讨温州地区人群中ER-α基因MSPⅠ多态性与子宫内膜癌遗传易感性的关系。方法应用聚合酶链式反应-限制性片段长度多态性分析技术,对48例子宫内膜癌患者和96例健康体检者进行ER-α基因MSPⅠ多态性检测,并分析该基因多态性与子宫内膜癌发病风险的关系。结果 ER-α基因MSPⅠ多态性位点基因型频率及等位基因频率在子宫内膜癌组分别为TT(58.3%)、CC(10.4%)、TC(31.2%);T(74.0%)、C(26.0%);对照组分别为TT(31.2%)、CC(24.0%)、TC(44.8%);T (53.6%)、C(46.4%),两组间比较均有统计学差异(均P<0.05),且子宫内膜癌组等位基因C频率低于对照组(P<0.01)。结论ER-α基因MSPⅠ位点多态性的存在可能与子宫内膜癌易感性有关,且ER-α基因野生型(TT)可能是子宫内膜癌的危险因素。
目的探討溫州地區人群中ER-α基因MSPⅠ多態性與子宮內膜癌遺傳易感性的關繫。方法應用聚閤酶鏈式反應-限製性片段長度多態性分析技術,對48例子宮內膜癌患者和96例健康體檢者進行ER-α基因MSPⅠ多態性檢測,併分析該基因多態性與子宮內膜癌髮病風險的關繫。結果 ER-α基因MSPⅠ多態性位點基因型頻率及等位基因頻率在子宮內膜癌組分彆為TT(58.3%)、CC(10.4%)、TC(31.2%);T(74.0%)、C(26.0%);對照組分彆為TT(31.2%)、CC(24.0%)、TC(44.8%);T (53.6%)、C(46.4%),兩組間比較均有統計學差異(均P<0.05),且子宮內膜癌組等位基因C頻率低于對照組(P<0.01)。結論ER-α基因MSPⅠ位點多態性的存在可能與子宮內膜癌易感性有關,且ER-α基因野生型(TT)可能是子宮內膜癌的危險因素。
목적탐토온주지구인군중ER-α기인MSPⅠ다태성여자궁내막암유전역감성적관계。방법응용취합매련식반응-한제성편단장도다태성분석기술,대48례자궁내막암환자화96례건강체검자진행ER-α기인MSPⅠ다태성검측,병분석해기인다태성여자궁내막암발병풍험적관계。결과 ER-α기인MSPⅠ다태성위점기인형빈솔급등위기인빈솔재자궁내막암조분별위TT(58.3%)、CC(10.4%)、TC(31.2%);T(74.0%)、C(26.0%);대조조분별위TT(31.2%)、CC(24.0%)、TC(44.8%);T (53.6%)、C(46.4%),량조간비교균유통계학차이(균P<0.05),차자궁내막암조등위기인C빈솔저우대조조(P<0.01)。결론ER-α기인MSPⅠ위점다태성적존재가능여자궁내막암역감성유관,차ER-α기인야생형(TT)가능시자궁내막암적위험인소。
Objective To assess the association of ER- α gene polymorphisms with endometrial cancer. Methods A case- control study was performed with 48 endometrial cancer patients and 96 matched controls. The ER- α- MSPⅠ polymor-phism sites were detected by using polymerase chain reaction- restriction fragment length polymorphism(PCR- RFLP). The asso-ciation between genotypes and endometrial cancer was estimated by odds ratios (ORs) and the 95% confidence intervals(CIs) calculated by unconditional logistic regression. Results The distribution frequency of genotype of ER- α- MSPⅠ site in en-dometrial cancer patients and controls was TT:58.3%and 31.2%, CC:10.4%and 24.0%, TC:31.2%and 44.8%, respectively;the frequency of al elic gene was T:74.0%and 53.6%, C:26.0%and 46.4%, respectively. There were significant differences in geno-type distributions between two groups (P<0.05), and the frequency of al elic C in endometrial cancer patients was lower than that of controls. Conclusion There may be association of ER- α- MSPⅠsite polymorphism with susceptibility of endometrial cancer.