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作 者:姜学革[1] 李晓瑛[1] 吕亚莉[1] 赵坡[1]
出 处:《中华肿瘤防治杂志》2013年第22期1724-1727,共4页Chinese Journal of Cancer Prevention and Treatment
摘 要:目的:总结分析荧光原位杂交(fluorescence in situ hybridization,FISH)技术检测乳腺髓样癌HER-2基因扩增的经验和临床病理学意义。方法:用FISH和免疫组化技术诊断32例乳腺髓样癌患者HER-2基因状态,并分析典型髓样癌和非典型髓样癌HER-2基因扩增的关系。结果:乳腺髓样癌HER-2基因扩增阳性率为37.5%(12/32),其中典型髓样癌为7.7%(1/13),非典型髓样癌为57.9%(11/19)。HER-2基因扩增与髓样癌肿瘤类型(P=0.008)、肿瘤大小(P=0.040)、淋巴结转移(P=0.006)、临床分期(P=0.037)、HER-2蛋白表达(P=0.000 1)和p53蛋白表达(P=0.015)有关,与患者年龄(P=0.438)、ER(P=0.081)和PR(P=0.517)无关。乳腺髓样癌类型与HER-2蛋白表达有关(P=0.010),与患者年龄(P=0.426)、肿瘤大小(P=0.786)、淋巴结转移(P=0.115)、临床分期(P=0.129)、ER(P=0.116)、PR(P=0.773)和p53(P=0.280)无关。结论:HER-2基因扩增可能参与乳腺髓样癌的演化与进展,乳腺典型髓样癌与非典型髓样癌的HER-2基因扩增有显著性差异,临床应用FISH技术诊断HER-2基因扩增靶标有助于指导乳腺非典型髓样癌的分子靶向治疗。OBJECTIVE: To summarize and analyze the experience and clinicopathological significance in application of fluorescence in situ hybridization (FISH) technique to diagnose HER-2 gene amplification in uncommon medullary car- cinoma of breast, and analyze the possible relationship between HER-2 gene amplification and type of medullary carcinoma as typical medullary carcinoma and atypical medullary carcinoma. METHODS: Status of HER-2 gene amplification was di agnosed by FISH technique and analyzed with other biomarkers and clincopathological data in 32 cases of medullary carci- noma of breast. RESULTS: The positive rate for HER-2 gene amplification was 37.5 % (12/32) ,in which typical medul- lary carcinoma was 7. 7% ( 1 / 13 ) and atypical medullary carcinoma was 57. 9 % ( 11/19 ), respectively. Amplification of HER-2 gene was correlative positively with the type of medullary carcinoma (P=0. 008), HER-2 protein expression (P= 0. 000 1), tumor size (P=0. 040), lymphatic metastasis (P = 0. 006), clinical stage (P = 0. 037) and p53 (P = 0. 015), whereas not with age (P=0. 438) ,ER(P=0. 081) and PR(P=0. 517). The type of medullary carcinoma of breast was correlative with HER-2 protein(P=0. 010), but not with age(P= 0. 426), tumor size(P= 0. 786), lymphatic metastasis (P=0. 115),clinical stage (P=0. 129),ER(P=0. 116),PR(P=0. 773)and P53(P=0. 280). CONCLUSIONS: Amplifi cation of HER-2 gene may be involved in evolution and progress of breast medullary carcinoma. There is a significant difference in HER-2 gene amplification between the typical type and the atypical type of medullary carcinoma of breast. Clinical application of FISH technique to diagnose the target of HER-2 gene amplification may be helpful to direct molecu lar targeting therapy in breast atypical medullary carcinoma patients.
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