Expression of basal keratins and vimentin in breast cancers of young women correlates with adverse pathologic parameters

被引:42
作者
Chen, Maureen Hong-Sing [1 ]
Yip, George Wai-Cheong [1 ]
Tse, Gary Man-Kit [2 ]
Moriya, Takuya [4 ]
Lui, Philip Chi-Wai [2 ]
Zin, Mar-Lwin [1 ]
Bay, Boon-Huat [1 ]
Tan, Puay-Hoon [1 ,3 ,5 ]
机构
[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Anat, Singapore 117595, Singapore
[2] Univ Hong Kong, Dept Anat & Cellular Pathol, Hong Kong, Hong Kong, Peoples R China
[3] Singapore Gen Hosp, Dept Pathol, Singapore 0316, Singapore
[4] Tohoku Univ, Dept Pathol, Sendai, Miyagi 980, Japan
[5] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Pathol, Singapore 117595, Singapore
关键词
young women; invasive breast cancer; basal keratins; vimentin; pathological parameters;
D O I
10.1038/modpathol.2008.90
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Previous studies have suggested that breast cancer in young women has more aggressive biological features and poorer prognosis. However, the role of biological markers in these patients is not well understood. We aimed to learn more about this disease in a cohort of 125 young women from Singapore, Japan and Hong Kong, aged 35 years or less, with invasive breast cancer by evaluating the expression of vimentin and the basal cytokeratins CK14, CK5/6 and 34 beta E12. Both standard paraffin sections and tissue microarrays were used in the immunohistochemical evaluation of expression patterns of these four biological markers. CK5/6, CK14, vimentin and 34 beta E12, in increasing order of proportion, were detected in invasive carcinomas. Basal cytokeratins and vimentin showed significant inverse relationship with estrogen and progesterone receptor status while CK14 expression was found to be directly associated with c-erbB2 status. Basal cytokeratins and vimentin immunoreactivities were directly associated with CD117 and EGFR expression. Vimentin and 34 beta E12 immunopositivity correlated with tumor size, while vimentin was associated with higher histological grade. Our findings are in concert with reports that expression of basal cytokeratins and vimentin is correlated with adverse pathological parameters.
引用
收藏
页码:1183 / 1191
页数:9
相关论文
共 37 条
[1]   Ductal carcinoma in situ with basal-like phenotype:: a possible precursor to invasive basal-like breast cancer [J].
Bryan, BB ;
Schnitt, SJ ;
Collins, LC .
MODERN PATHOLOGY, 2006, 19 (05) :617-621
[2]   Molecular classification of breast carcinomas using tissue microarrays [J].
Callagy, G ;
Cattaneo, E ;
Daigo, Y ;
Happerfield, L ;
Bobrow, LG ;
Pharoah, PDP ;
Caldas, C .
DIAGNOSTIC MOLECULAR PATHOLOGY, 2003, 12 (01) :27-34
[3]   Immunohistochemical biomarkers in patients with early-onset breast carcinoma by tissue microarray [J].
Choi, DH ;
Kim, S ;
Rimm, DL ;
Carter, D ;
Haffty, BG .
CANCER JOURNAL, 2005, 11 (05) :404-411
[4]   Very young women (<35 years) with operable breast cancer:: features of disease at presentation [J].
Colleoni, M ;
Rotmensz, N ;
Robertson, C ;
Orlando, L ;
Viale, G ;
Renne, G ;
Luini, A ;
Veronesi, P ;
Intra, M ;
Orecchia, R ;
Catalano, G ;
Galimberti, V ;
Nolé, F ;
Martinelli, G ;
Goldhirsch, A .
ANNALS OF ONCOLOGY, 2002, 13 (02) :273-279
[5]   EXPRESSION OF BASAL AND LUMINAL EPITHELIUM-SPECIFIC KERATINS IN NORMAL, BENIGN, AND MALIGNANT BREAST-TISSUE [J].
DAIRKEE, SH ;
PUETT, L ;
HACKETT, AJ .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1988, 80 (09) :691-695
[6]   C-KIT expression in ductal carcinoma in situ of the breast: co-expression with HER-2/neu [J].
Diallo, R ;
Rody, A ;
Jackisch, C ;
Ting, E ;
Schaefer, KL ;
Kissler, S ;
Karn, T ;
Geddert, H ;
Engels, K ;
Kaufmann, M ;
Gabbert, HE ;
Shroyer, KR ;
Poremba, C .
HUMAN PATHOLOGY, 2006, 37 (02) :205-211
[7]  
DOMAGALA W, 1986, ACTA CYTOL, V30, P214
[8]  
DOMAGALA W, 1990, AM J PATHOL, V137, P1299
[9]   Expression of luminal and basal cytokeratins in human breast carcinoma [J].
El-Rehim, DMA ;
Pinder, SE ;
Paish, CE ;
Bell, J ;
Blamey, R ;
Robertson, JFR ;
Nicholson, RI ;
Ellis, IO .
JOURNAL OF PATHOLOGY, 2004, 203 (02) :661-671
[10]   Breast carcinoma in women 35 years and younger: a pathological study [J].
Fernandopulle, Shanika M. ;
Ang, Peter Cher-Siang ;
Tan, Puay Hoon .
PATHOLOGY, 2006, 38 (03) :219-222