蚌埠医学院学报
蚌埠醫學院學報
방부의학원학보
Journal of Bengbu Medical College
2015年
10期
1301-1304
,共4页
赵遵兰%卢晓辉%王洋洋%吴海华%夏春磊%陈素莲%杨清玲%陈昌杰
趙遵蘭%盧曉輝%王洋洋%吳海華%夏春磊%陳素蓮%楊清玲%陳昌傑
조준란%로효휘%왕양양%오해화%하춘뢰%진소련%양청령%진창걸
乳腺肿瘤%微小RNA-125b%信号素分子4C
乳腺腫瘤%微小RNA-125b%信號素分子4C
유선종류%미소RNA-125b%신호소분자4C
breast neoplasms%microRNA-125b%semaphorin 4C
目的:探讨微小RNA(microRNA,miR)-125b及其靶基因信号素分子(SEMA)4C在乳腺癌组织(BRCR)及其癌旁正常组织(NCT)中的表达情况,并分析其与临床病理学特征的关联性及意义.方法:采用荧光定量PCR检测24 例BRCR及其NCT中miR-125b的表达,采用免疫组织化学方法检测40例BRCR及其NCT中SEMA4C的表达.统计分析两者表达水平与患者的年龄、组织学分级、临床分期、淋巴结转移,雌、孕激素受体和人表皮生长因子受体-2(cerbB-2)等临床病理学特征间的关联性.结果:SEMA4C表达在BRCR中高于NCT,SEMA4C表达在淋巴结转移和cerbB-2表达间差异均有统计学意义(P<0.01和P<0.05),而在患者年龄,组织学分级,肿瘤临床分期及雌、孕激素受体表达间差异均无统计学意义(P>0.05).miR-125b表达在BRCR中低于NCT(P<0.05),其表达在SEMA4C、淋巴结转移以及cerbB-2差异均有统计学意义(P=0.034 ~P=0.022).结论:在乳腺浸润性导管癌中SEMA4C表达升高,miR-125b表达降低,两者均与cerbB-2过表达以及淋巴结转移均有一定关系,提示SEMA4C为miR-125b靶基因之一,miR-125b可能是一个新的乳腺癌标志物.
目的:探討微小RNA(microRNA,miR)-125b及其靶基因信號素分子(SEMA)4C在乳腺癌組織(BRCR)及其癌徬正常組織(NCT)中的錶達情況,併分析其與臨床病理學特徵的關聯性及意義.方法:採用熒光定量PCR檢測24 例BRCR及其NCT中miR-125b的錶達,採用免疫組織化學方法檢測40例BRCR及其NCT中SEMA4C的錶達.統計分析兩者錶達水平與患者的年齡、組織學分級、臨床分期、淋巴結轉移,雌、孕激素受體和人錶皮生長因子受體-2(cerbB-2)等臨床病理學特徵間的關聯性.結果:SEMA4C錶達在BRCR中高于NCT,SEMA4C錶達在淋巴結轉移和cerbB-2錶達間差異均有統計學意義(P<0.01和P<0.05),而在患者年齡,組織學分級,腫瘤臨床分期及雌、孕激素受體錶達間差異均無統計學意義(P>0.05).miR-125b錶達在BRCR中低于NCT(P<0.05),其錶達在SEMA4C、淋巴結轉移以及cerbB-2差異均有統計學意義(P=0.034 ~P=0.022).結論:在乳腺浸潤性導管癌中SEMA4C錶達升高,miR-125b錶達降低,兩者均與cerbB-2過錶達以及淋巴結轉移均有一定關繫,提示SEMA4C為miR-125b靶基因之一,miR-125b可能是一箇新的乳腺癌標誌物.
목적:탐토미소RNA(microRNA,miR)-125b급기파기인신호소분자(SEMA)4C재유선암조직(BRCR)급기암방정상조직(NCT)중적표체정황,병분석기여림상병이학특정적관련성급의의.방법:채용형광정량PCR검측24 례BRCR급기NCT중miR-125b적표체,채용면역조직화학방법검측40례BRCR급기NCT중SEMA4C적표체.통계분석량자표체수평여환자적년령、조직학분급、림상분기、림파결전이,자、잉격소수체화인표피생장인자수체-2(cerbB-2)등림상병이학특정간적관련성.결과:SEMA4C표체재BRCR중고우NCT,SEMA4C표체재림파결전이화cerbB-2표체간차이균유통계학의의(P<0.01화P<0.05),이재환자년령,조직학분급,종류림상분기급자、잉격소수체표체간차이균무통계학의의(P>0.05).miR-125b표체재BRCR중저우NCT(P<0.05),기표체재SEMA4C、림파결전이이급cerbB-2차이균유통계학의의(P=0.034 ~P=0.022).결론:재유선침윤성도관암중SEMA4C표체승고,miR-125b표체강저,량자균여cerbB-2과표체이급림파결전이균유일정관계,제시SEMA4C위miR-125b파기인지일,miR-125b가능시일개신적유선암표지물.
Objective:To explore the expressions of microRNA(miR)-125b and its target gene semaphorin4C(SEMA4C) in breast cancer tissue(BRCR) and adjacent normal tissue(NCT),and analyze its correlation with clinicopathologic features and significance. Methods:The expressions of miR-125b in 24 BRCR and NCT were detected using real-time quantitative PCR,and the expressions of SEMA4C in 40 BRCR and NCT were detected by immunohistochemistry. The relationships between the expressions of miR-125b and SEMA4C and clinico-pathological parameters including age,clinical staging,lymph node metastasis,estrogen receptor,progesterone and human epidermal growth factor receptor-2(cerbB-2) were analyzed. Results:The expression of SEMA4C in BRCR was higher than that in NCT,the difference between the expression of SEMA4C and cerbB-2 in lymph node metastasis tissue was statistically significant(P<0. 01 and P<0. 05). The differences of the age,histological grading,clinical staging,and estrogen and progesterone receptors were not statistically significant(P>0. 05). The expression of miR-125b in BRCR was lower than that in NCT(P <0. 05),the differences between the expression of SEMA4C and cerbB-2 in lymph node metastasis tissue were statistically significant ( P =0. 034 to P =0. 022). Conclusions:The expressions of miR-125b and SEMA4C in breast invasive ductal carcinoma increase and decrease, respectively,which is associated with lymph node metastasis and cerbB-2 level. The SEMA4C is one target gene of miR-125b,and miR-125b may serve as a potential breast cancer marker.