东南国防医药
東南國防醫藥
동남국방의약
JOURNAL OF SOUTHEAST CHINA NATIONAL DEFENCE MEDICAL SCIENCE
2015年
1期
22-25
,共4页
乳腺癌%微小核糖核酸%多态性
乳腺癌%微小覈糖覈痠%多態性
유선암%미소핵당핵산%다태성
breast cancer%microRNA%polymorphism
目的:探讨6个微小 RNA ( microRNA )多态性位点( rs11614913, microRNA-196a2;rs3746444, hsa-mir-499;rs2910164,microRNA-146a;rs2292832,microRNA-149;rs6505162,microRNA-423;rs895819,microRNA-27a)与中国女性乳腺癌发病风险及病理特征的相关性。方法采用病例对照研究,选取350例乳腺癌患者为病例组及350名正常女性为对照组,采用Massarray SNP技术检测6个多态性位点的基因型,采用免疫组化法检测乳腺癌组织中的雌激素受体及孕激素受体表达,分析各基因型与乳腺癌发生的关系及与乳腺癌病理参数的关系。结果 rs3746444GG基因型在病例组中(OR=1.71,95%CI:1.16~2.52)的频率显著高于对照组。分层分析结果显示,在绝经后的人群中,rs3746444GG基因型病例组中的频率( OR=2.19,95%CI:1.16~4.15)显著高于对照组。 rs3746444GG基因型在肿瘤分期0~Ⅱ组(OR=1.92,95%CI:1.17~3.13)、淋巴结转移组(OR=2.20,95%CI:1.28~3.79)、孕激素受体阴性组中(OR=2.19,95%CI:1.25~3.82)分布频率均显著高于正常对照组。在绝经后人群中,rs2910164GG基因型在病例组中(OR=2.19,95%CI:1.16~4.15)的分布频率显著高于对照组。而在绝经前的人群中,rs2910164GG基因型在病例组中( OR=0.49,95%CI:0.25~0.98)的分布频率显著低于对照组。结论rs3746444GG基因型与乳腺癌发病风险相关,特别是在绝经后人群中风险更高。 rs2910164GG基因型与乳腺癌的发病风险相关性与妇女是否绝经有关。
目的:探討6箇微小 RNA ( microRNA )多態性位點( rs11614913, microRNA-196a2;rs3746444, hsa-mir-499;rs2910164,microRNA-146a;rs2292832,microRNA-149;rs6505162,microRNA-423;rs895819,microRNA-27a)與中國女性乳腺癌髮病風險及病理特徵的相關性。方法採用病例對照研究,選取350例乳腺癌患者為病例組及350名正常女性為對照組,採用Massarray SNP技術檢測6箇多態性位點的基因型,採用免疫組化法檢測乳腺癌組織中的雌激素受體及孕激素受體錶達,分析各基因型與乳腺癌髮生的關繫及與乳腺癌病理參數的關繫。結果 rs3746444GG基因型在病例組中(OR=1.71,95%CI:1.16~2.52)的頻率顯著高于對照組。分層分析結果顯示,在絕經後的人群中,rs3746444GG基因型病例組中的頻率( OR=2.19,95%CI:1.16~4.15)顯著高于對照組。 rs3746444GG基因型在腫瘤分期0~Ⅱ組(OR=1.92,95%CI:1.17~3.13)、淋巴結轉移組(OR=2.20,95%CI:1.28~3.79)、孕激素受體陰性組中(OR=2.19,95%CI:1.25~3.82)分佈頻率均顯著高于正常對照組。在絕經後人群中,rs2910164GG基因型在病例組中(OR=2.19,95%CI:1.16~4.15)的分佈頻率顯著高于對照組。而在絕經前的人群中,rs2910164GG基因型在病例組中( OR=0.49,95%CI:0.25~0.98)的分佈頻率顯著低于對照組。結論rs3746444GG基因型與乳腺癌髮病風險相關,特彆是在絕經後人群中風險更高。 rs2910164GG基因型與乳腺癌的髮病風險相關性與婦女是否絕經有關。
목적:탐토6개미소 RNA ( microRNA )다태성위점( rs11614913, microRNA-196a2;rs3746444, hsa-mir-499;rs2910164,microRNA-146a;rs2292832,microRNA-149;rs6505162,microRNA-423;rs895819,microRNA-27a)여중국녀성유선암발병풍험급병리특정적상관성。방법채용병례대조연구,선취350례유선암환자위병례조급350명정상녀성위대조조,채용Massarray SNP기술검측6개다태성위점적기인형,채용면역조화법검측유선암조직중적자격소수체급잉격소수체표체,분석각기인형여유선암발생적관계급여유선암병리삼수적관계。결과 rs3746444GG기인형재병례조중(OR=1.71,95%CI:1.16~2.52)적빈솔현저고우대조조。분층분석결과현시,재절경후적인군중,rs3746444GG기인형병례조중적빈솔( OR=2.19,95%CI:1.16~4.15)현저고우대조조。 rs3746444GG기인형재종류분기0~Ⅱ조(OR=1.92,95%CI:1.17~3.13)、림파결전이조(OR=2.20,95%CI:1.28~3.79)、잉격소수체음성조중(OR=2.19,95%CI:1.25~3.82)분포빈솔균현저고우정상대조조。재절경후인군중,rs2910164GG기인형재병례조중(OR=2.19,95%CI:1.16~4.15)적분포빈솔현저고우대조조。이재절경전적인군중,rs2910164GG기인형재병례조중( OR=0.49,95%CI:0.25~0.98)적분포빈솔현저저우대조조。결론rs3746444GG기인형여유선암발병풍험상관,특별시재절경후인군중풍험경고。 rs2910164GG기인형여유선암적발병풍험상관성여부녀시부절경유관。
Objective To investigate the relationship between the polymorphisms in microRNAs ( rs11614913, miRNA-196a2;rs3746444, hsa-mir-499;rs2910164, miRNA-146a;rs2292832, miRNA-149;rs6505162, miRNA-423;rs895819, miRNA-27a) and risk and pathologic characterize of breast cancer in Chinese female population .Methods A total of 350 patients with breast cancer and 350 health controls were enrolled for this case-controls study .Sequenom MassARRAY was applied to detect the polymor-phisms, and the immunohistochemistry assay was used to measure the expression of estrogen receptor (ER) and progesterone receptor ( PR) .Logistic regression was applied to assess the association between the polymorphisms and risk and pathologic characterize of breast cancer.Results The results showed that the frequency of 3746444GG genotype(OR=1.71, 95%CI:1.16-2.52) was high-er in cases than that in health controls .Sub-group analysis revealed that , in the subgroup of women with postmenopausal status , the frequency of 3746444GG genotype (OR=2.19, 95%CI:1.16-4.15) was higher in cases than that in health controls .Moreover, the frequency of 3746444GG was higher in subgroup of patients with tumor stage 0-Ⅱ(OR=1.92, 95%CI:1.17-3.13), lymph node involvement(OR=2.20, 95%CI:1.28-3.79), negative PR expression (OR=2.19, 95% CI:1.25-3.82) than that in health controls, respectively.In addition, rs2910164GG genotype(OR=2.19, 95%CI:1.16-4.15) was associated with increased breast cancer risk in the postmenopausal status sub-cohort, while, rs2910164GG genotype (OR=0.49, 95%CI:0.25-0.98) was associated with decreased breast cancer risk in the premenopausal status sub -cohort.Conclusion rs3746444GG genotype was associ-ated with breast cancer risk , especiallyfor women who with postmenopausal status .The risk of rs2910164GG for breast cancer was mod-ified by the postmenopausal status .