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Basal-HER2 phenotype shows poorer survival than basal-like phenotype in hormone receptor-negative invasive breast cancers.

Basal-HER2 phenotype shows poorer survival than basal-like phenotype in hormone receptor-negative invasive breast cancers. Research Abstract Details 

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  • Basal-HER2 phenotype shows poorer survival than basal-like phenotype in hormone receptor-negative invasive breast cancers. Abstract Text:

    hui liuHui Liu,qinhe fanQinhe Fan,zhihong zhangZhihong Zhang,xiao liXiao Li,huiping yuHuiping Yu,fanqing mengFanqing Meng,hui liuHui Liu,qinhe fanQinhe Fan,zhihong zhangZhihong Zhang,xiao liXiao Li,huiping yuHuiping Yu,fanqing mengFanqing Meng,hui liuHui Liu,qinhe fanQinhe Fan,zhihong zhangZhihong Zhang,xiao liXiao Li,huiping yuHuiping Yu,fanqing mengFanqing Meng,

    Previous studies have shown conflicting results on prognostic significance of basal-like breast tumors, but hormone receptor is a confusing factor in most of the prognostic evaluations. We aimed to characterize the prognostic features of basal-like tumors without the influence of hormone receptor status in a series of hormone receptor-negative breast tumors. Using tissue microarray and immunohistochemistry methods, according to the expression of HER2 and basal markers (CK5/6, CK14, EGFR), we categorized 713 consecutive hormone receptor-negative invasive breast cancers into 3 subtypes: HER2 (HER2+), basal-like (HER2-, any basal marker+), and null (HER2-, all basal markers-). The HER2 phenotype was subdivided into pure-HER2 (HER2+, all basal markers-) and basal-HER2 (HER2+, any basal marker+) subgroups. Expression of p53, p63, vimentin, and BRCA1 was assessed immunochemically. Basal-like tumors showed significantly higher grade, more frequent recurrence, and higher expression of vimentin and p63 than HER2 and null phenotypes. Basal-HER2 phenotype had significantly younger mean age and expressed a higher level of p53 and vimentin like basal-like and/or HER2 phenotypes. However, unlike all the other hormone receptor-negative phenotypes, they highly expressed BRCA1. No significant difference was found in 5-year survival among basal-like and the other hormone receptor-negative phenotypes, except for basal-HER2, which showed poorer 5-year overall survival than basal-like tumors. In conclusion, although basal-like breast tumors have distinct clinicopathologic and immunohistochemical features, they have similar 5-year survival compared with the other hormone receptor-negative tumors including HER2 and null phenotypes. However, there exists a small group of hormone receptor-negative tumors expressing HER2 and basal markers simultaneously. This small group of tumors showed significantly poorer 5-year overall survival than basal-like breast tumors and might require different treatment strategy.

    Basal-HER2 phenotype shows poorer survival than basal-like phenotype in hormone receptor-negative invasive breast cancers. Publishing Authors By Initials

    h liuH Liu,q fanQ Fan,z zhangZ Zhang,x liX Li,h yuH Yu,f mengF Meng,h liuH Liu,q fanQ Fan,z zhangZ Zhang,x liX Li,h yuH Yu,f mengF Meng,h liuH Liu,q fanQ Fan,z zhangZ Zhang,x liX Li,h yuH Yu,f mengF Meng,

    For similar abstracts research abstracts see: abstracts research

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    Basal-HER2 phenotype shows poorer survival than basal-like phenotype in hormone receptor-negative invasive breast cancers. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Human pathology

    VOLUME: 39

    Page Numbers: 167-74

    Journal Abbreviation: Hum. Pathol.

    ISSN: 0046-8177

    DAY: 28

    MONTH: 11

    YEAR: 2007

    Basal-HER2 phenotype shows poorer survival than basal-like phenotype in hormone receptor-negative invasive breast cancers. Information

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    LANGUAGE: eng

    NlmUniqueID: 9421547

    Basal-HER2 phenotype shows poorer survival than basal-like phenotype in hormone receptor-negative invasive breast cancers. Keywords Mesh Terms:

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    Grant and Affiliation Information for Basal-HER2 phenotype shows poorer survival than basal-like phenotype in hormone receptor-negative invasive breast cancers.

    AFFILIATION: Department of Pathology, Nanjing Medical University, Nanjing 210029, PR China.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Hum Pathol

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