中华临床医师杂志(电子版)
中華臨床醫師雜誌(電子版)
중화림상의사잡지(전자판)
CHINESE JOURNAL OF CLINICIANS(ELECTRONIC VERSION)
2013年
15期
6949-6953
,共5页
傅韵%蒋蓓琦%武羿%王奕静%成小林%李正东%庄志刚
傅韻%蔣蓓琦%武羿%王奕靜%成小林%李正東%莊誌剛
부운%장배기%무예%왕혁정%성소림%리정동%장지강
左炔诺孕酮%乳腺肿瘤%宫内缓释系统%他莫西芬%子宫内膜病变
左炔諾孕酮%乳腺腫瘤%宮內緩釋繫統%他莫西芬%子宮內膜病變
좌결낙잉동%유선종류%궁내완석계통%타막서분%자궁내막병변
Levonorgestrel%Breast neoplasms%Releasing intrauterine system%Tamoxifen%Endometrial lesion
目的:探讨左炔诺孕酮宫内缓释系统(LNG-IUS)与他莫西芬引起的子宫内膜病变间的相关性。方法收集2010年10月至2011年7月经病理学证实为浸润性导管癌的术后服用他莫西芬的30例绝经前乳腺癌患者在放置LNG-IUS前后的子宫内膜组织,用real-time PCR和Western blot法检测PTEN、PAX-2、Ki-67和K-ras的表达情况,并在放置LNG-IUS后3、6、12个月行超声随访患者放环前后的子宫内膜情况。结果(1)相比放置LNG-IUS前的子宫内膜厚度[(12.55±2.52)mm],放置LNG-IUS后子宫内膜3个月[(10.30±1.90)mm,t=12.795,P=0.000]、6个月[(9.10±1.25)mm,t=7.384,P=0.000]、12个月[(7.30±0.87)mm,t=9.769,P=0.000]均受到明显抑制;(2)通过对子宫内膜行定量PCR检测发现相较放环前的表达,随着放置LNG-IUS时间延长,PTEN逐渐增高:在放环6个月及12个月时出现统计学差异(t=-2.401,P=0.023;t=-5.579,P=0.031);K-ras的表达逐渐降低:在放环12个月时出现统计学差异(t=7.064,P=0.019);Ki-67的表达逐渐降低:在放置6个月及12个月时出现统计学差异(t=4.615, P=0.044;t=6.817,P=0.021);而PAX2的表达虽降低,但无统计学差异;(3)通过Western blot检测亦发现随着放置LNG-IUS的时间延长,PTEN表达增强,在放环6个月及12个月时出现统计学差异(t=-8.928,P=0.012;t=-4.489,P=0.046);K-ras表达降低:在放环12个月时出现统计学差异(t=7.965,P=0.015);Ki-67的表达降低:在放置6个月及12个月时出现统计学差异(t=15.600,P=0.004;t=7.730,P=0.016),而PAX-2的表达未及明显改变(P>0.05)。结论 LNG-IUS能降低他莫西芬引起的子宫内膜病变。
目的:探討左炔諾孕酮宮內緩釋繫統(LNG-IUS)與他莫西芬引起的子宮內膜病變間的相關性。方法收集2010年10月至2011年7月經病理學證實為浸潤性導管癌的術後服用他莫西芬的30例絕經前乳腺癌患者在放置LNG-IUS前後的子宮內膜組織,用real-time PCR和Western blot法檢測PTEN、PAX-2、Ki-67和K-ras的錶達情況,併在放置LNG-IUS後3、6、12箇月行超聲隨訪患者放環前後的子宮內膜情況。結果(1)相比放置LNG-IUS前的子宮內膜厚度[(12.55±2.52)mm],放置LNG-IUS後子宮內膜3箇月[(10.30±1.90)mm,t=12.795,P=0.000]、6箇月[(9.10±1.25)mm,t=7.384,P=0.000]、12箇月[(7.30±0.87)mm,t=9.769,P=0.000]均受到明顯抑製;(2)通過對子宮內膜行定量PCR檢測髮現相較放環前的錶達,隨著放置LNG-IUS時間延長,PTEN逐漸增高:在放環6箇月及12箇月時齣現統計學差異(t=-2.401,P=0.023;t=-5.579,P=0.031);K-ras的錶達逐漸降低:在放環12箇月時齣現統計學差異(t=7.064,P=0.019);Ki-67的錶達逐漸降低:在放置6箇月及12箇月時齣現統計學差異(t=4.615, P=0.044;t=6.817,P=0.021);而PAX2的錶達雖降低,但無統計學差異;(3)通過Western blot檢測亦髮現隨著放置LNG-IUS的時間延長,PTEN錶達增彊,在放環6箇月及12箇月時齣現統計學差異(t=-8.928,P=0.012;t=-4.489,P=0.046);K-ras錶達降低:在放環12箇月時齣現統計學差異(t=7.965,P=0.015);Ki-67的錶達降低:在放置6箇月及12箇月時齣現統計學差異(t=15.600,P=0.004;t=7.730,P=0.016),而PAX-2的錶達未及明顯改變(P>0.05)。結論 LNG-IUS能降低他莫西芬引起的子宮內膜病變。
목적:탐토좌결낙잉동궁내완석계통(LNG-IUS)여타막서분인기적자궁내막병변간적상관성。방법수집2010년10월지2011년7월경병이학증실위침윤성도관암적술후복용타막서분적30례절경전유선암환자재방치LNG-IUS전후적자궁내막조직,용real-time PCR화Western blot법검측PTEN、PAX-2、Ki-67화K-ras적표체정황,병재방치LNG-IUS후3、6、12개월행초성수방환자방배전후적자궁내막정황。결과(1)상비방치LNG-IUS전적자궁내막후도[(12.55±2.52)mm],방치LNG-IUS후자궁내막3개월[(10.30±1.90)mm,t=12.795,P=0.000]、6개월[(9.10±1.25)mm,t=7.384,P=0.000]、12개월[(7.30±0.87)mm,t=9.769,P=0.000]균수도명현억제;(2)통과대자궁내막행정량PCR검측발현상교방배전적표체,수착방치LNG-IUS시간연장,PTEN축점증고:재방배6개월급12개월시출현통계학차이(t=-2.401,P=0.023;t=-5.579,P=0.031);K-ras적표체축점강저:재방배12개월시출현통계학차이(t=7.064,P=0.019);Ki-67적표체축점강저:재방치6개월급12개월시출현통계학차이(t=4.615, P=0.044;t=6.817,P=0.021);이PAX2적표체수강저,단무통계학차이;(3)통과Western blot검측역발현수착방치LNG-IUS적시간연장,PTEN표체증강,재방배6개월급12개월시출현통계학차이(t=-8.928,P=0.012;t=-4.489,P=0.046);K-ras표체강저:재방배12개월시출현통계학차이(t=7.965,P=0.015);Ki-67적표체강저:재방치6개월급12개월시출현통계학차이(t=15.600,P=0.004;t=7.730,P=0.016),이PAX-2적표체미급명현개변(P>0.05)。결론 LNG-IUS능강저타막서분인기적자궁내막병변。
Objective To explore the relation between Levonorgestrel-releasing intrauterine system(LNG-IUS) and tamoxifen induced endometrial lesions. Methods Thirty premenopausal breast cancer patients, who had taken tamoxifen as hormonal therapy after undergoing operations from October 2010 to July 2011 and were pathologically diagnosed as invasive ductal carcinoma, were enrolled to place levonorgestrel-releasing intrauterine system. The endometrial tissues of patients before and after placing ING-IUS were collected for detecting expression of PTEN, PAX2, Ki-67 and K-ras by real-time PCR and Western blot. The thickness of endometrium were detected by ultrasound at the point of three, six and twelve months after LNG-IUS was placed. Result (1)The endometrial thickness after LNG-IUS placed was significantly restrained[three months: (10.30±1.90)mm; six months: (9.10±1.25)mm; twelve months: (7.30±0.87)mm]compared to the endometrial thickness[(12.55± 2.52)mm]before LNG-IUS placed (three months: t=12.795, P=0.000; six months: t=7.384, P=0.000; twelve month: t=9.769, P=0.000). (2)By real-time PCR, with LNG-IUS progressing, the expression of PTEN was growing and had statistically differences at the point of six months and twelve point(t=-2.401, P=0.023,t=-5.579, P=0.031);the expression of K-ras was reducing and had difference at the point of twelve months (t=7.064, P=0.019);the expression of Ki-67 was declining and had differences at the point of six months and twelve months (t=4.615, P=0.044 , t=6.817, P=0.021);but expression of PAX2 didn't have any statistically difference though decreased. (3) By immunoblotting, the expression of PTEN was increased and had statistically differences at the point of six months and twelve point (t=-8.928, P=0.012, t=-4.489, P=0.046);that of K-ras was decreased and had difference at the point of twelve months (t=7.965, P=0.015)and Ki-67 was declining and had differences at the point of six months and twelve months (t=15.600, P=0.004,t=7.730, P=0.016); But the expression of PAX-2 was similar(P>0.05). Conclusion Levonorgestrel-releasing intrauterine system lessens the endometrial lesions induced by Tamoxifen.