中华皮肤科杂志
中華皮膚科雜誌
중화피부과잡지
Chinese Journal of Dermatology
2014年
12期
883-885
,共3页
任丹阳%康晓静%于世荣%时晓辉%吴秀娟%靳颖%普雄明
任丹暘%康曉靜%于世榮%時曉輝%吳秀娟%靳穎%普雄明
임단양%강효정%우세영%시효휘%오수연%근영%보웅명
黑色素瘤%突变%原癌基因蛋白质B-raf
黑色素瘤%突變%原癌基因蛋白質B-raf
흑색소류%돌변%원암기인단백질B-raf
Melanoma%Mutation%Proto-oncogene proteins B-raf
目的 探讨皮肤黑素瘤BRAF V600E突变蛋白表达情况,分析免疫组化法检测V600E突变的灵敏度和特异度.方法 应用抗BRAF V600E单克隆抗体的免疫组化法检测103例皮肤黑素瘤、40例色素痣石蜡包埋组织切片中BRAF V600E突变蛋白表达水平.采用SPSS 17.0统计软件进行统计分析,率的比较采用x2检验.结果 BRAF V600E突变蛋白阳性表达率在皮肤黑素瘤中为20.4%(21/103),色素痣中为5.0%(2/40),两组差异有统计学意义(x2=5.06,P< 0.05).黑素瘤BRAF V600E突变蛋白的表达率在不同年龄组[<60岁组表达率为29.8%(14/47),≥60岁组为12.5%(7/56)]、不同民族[维吾尔族组为30.2%(13/43),汉族组为13.3%(8/60)]、不同发病部位[肢端为13.6%(6/42)、黏膜为11.8% (4/29)、非肢端为45.8%(11/32)]、不同Clark分级[Ⅰ~Ⅲ级组为8.6%(4/42),Ⅳ~Ⅴ级组为12.4%(17/61)]组间表达差异均有统计学意义(P<0.05),而在不同性别、有无淋巴结转移组间表达差异均无统计学意义(P>0.05).免疫组化检测恶性黑素瘤中BRAF V600E突变灵敏度为100%(15/15),特异度为98.5%(65/66).结论 BRAF V600E突变蛋白在皮肤黑素瘤中高表达,在维吾尔族人群表达率高于汉族人群;免疫组化法检测BRAF V600E突变具有准确、快速等特点.
目的 探討皮膚黑素瘤BRAF V600E突變蛋白錶達情況,分析免疫組化法檢測V600E突變的靈敏度和特異度.方法 應用抗BRAF V600E單剋隆抗體的免疫組化法檢測103例皮膚黑素瘤、40例色素痣石蠟包埋組織切片中BRAF V600E突變蛋白錶達水平.採用SPSS 17.0統計軟件進行統計分析,率的比較採用x2檢驗.結果 BRAF V600E突變蛋白暘性錶達率在皮膚黑素瘤中為20.4%(21/103),色素痣中為5.0%(2/40),兩組差異有統計學意義(x2=5.06,P< 0.05).黑素瘤BRAF V600E突變蛋白的錶達率在不同年齡組[<60歲組錶達率為29.8%(14/47),≥60歲組為12.5%(7/56)]、不同民族[維吾爾族組為30.2%(13/43),漢族組為13.3%(8/60)]、不同髮病部位[肢耑為13.6%(6/42)、黏膜為11.8% (4/29)、非肢耑為45.8%(11/32)]、不同Clark分級[Ⅰ~Ⅲ級組為8.6%(4/42),Ⅳ~Ⅴ級組為12.4%(17/61)]組間錶達差異均有統計學意義(P<0.05),而在不同性彆、有無淋巴結轉移組間錶達差異均無統計學意義(P>0.05).免疫組化檢測噁性黑素瘤中BRAF V600E突變靈敏度為100%(15/15),特異度為98.5%(65/66).結論 BRAF V600E突變蛋白在皮膚黑素瘤中高錶達,在維吾爾族人群錶達率高于漢族人群;免疫組化法檢測BRAF V600E突變具有準確、快速等特點.
목적 탐토피부흑소류BRAF V600E돌변단백표체정황,분석면역조화법검측V600E돌변적령민도화특이도.방법 응용항BRAF V600E단극륭항체적면역조화법검측103례피부흑소류、40례색소지석사포매조직절편중BRAF V600E돌변단백표체수평.채용SPSS 17.0통계연건진행통계분석,솔적비교채용x2검험.결과 BRAF V600E돌변단백양성표체솔재피부흑소류중위20.4%(21/103),색소지중위5.0%(2/40),량조차이유통계학의의(x2=5.06,P< 0.05).흑소류BRAF V600E돌변단백적표체솔재불동년령조[<60세조표체솔위29.8%(14/47),≥60세조위12.5%(7/56)]、불동민족[유오이족조위30.2%(13/43),한족조위13.3%(8/60)]、불동발병부위[지단위13.6%(6/42)、점막위11.8% (4/29)、비지단위45.8%(11/32)]、불동Clark분급[Ⅰ~Ⅲ급조위8.6%(4/42),Ⅳ~Ⅴ급조위12.4%(17/61)]조간표체차이균유통계학의의(P<0.05),이재불동성별、유무림파결전이조간표체차이균무통계학의의(P>0.05).면역조화검측악성흑소류중BRAF V600E돌변령민도위100%(15/15),특이도위98.5%(65/66).결론 BRAF V600E돌변단백재피부흑소류중고표체,재유오이족인군표체솔고우한족인군;면역조화법검측BRAF V600E돌변구유준학、쾌속등특점.
Objective To detect the expression of BRAF V600E mutant protein in cutaneous malignant melanoma (CMM),and to evaluate the sensitivity and specificity of immunohistochemistry (IHC) in detecting BRAF V600E mutation.Methods IHC with an anti-BRAF V600E monoclonal antibody was performed to detect the expression of BRAF V600E mutant protein in paraffin-embedded tissue sections from 103 patients with CMM and 40 patients with nevus.Statistical analysis was carried out with SPSS software version 17.0,and the expression rate of BRAF V600E mutant protein was compared by chi-square test.Results The expression rate of BRAF V600E mutant protein in the CMM patients was 20.4% (21/103),significantly higher than that in the nevus patients (5.0% (2/40),x2 =5.06,P < 0.05).Significant differences were observed in the expression rate of BRAF V600E mutant protein between CMM patients of different age groups (29.8% (14/47) in patients aged < 60 years vs.12.5% (7/56) in those aged ≥ 60 years,P < 0.05) and nationality (30.2% (13/43) for Uygur nationality vs.13.3% (8/60) for Han nationality,P < 0.05),as well as among CMM lesions from different anatomical sites (13.6% (6/42) in acral sites vs.11.8% (4/29) in mucous membrane vs.45.8% (11/32) in non-acral sites,P < 0.05) and of different Clark levels (8.6% (4/42) for grade Ⅰ-Ⅲ vs.12.4% (17/61) for grade Ⅳ-Ⅴ,P< 0.05),but not between male and female CMM patients or between CMM patients with lymph node metastasis and those without (both P > 0.05).IHC with the anti-BRAF V600E antibody showed a sensitivity of 100% (15/15) and a specificity of 98.5% (65/66) in detecting BRAF V600E mutation.Conclusions The expression of BRAF V600E mutant protein is up-regulated in CMM lesions,and CMM patients of Uygur nationality seems to have a higher expression rate than those of Han nationality.IHC appears to be an accurate and rapid method to detect V600E BRAF mutation.