Cytokeratin and vimentin expression in breast cancer

被引:53
作者
Vora, Hemangini H. [1 ]
Patel, Nupur A.
Rajvik, Kruti N.
Mehta, Shalvi V.
Brahmbhatt, Birwa V.
Shah, Manoj J. [2 ]
Shukla, Shilin N.
Shah, Pankaj M.
机构
[1] Gujarat Canc Res Inst, Div Immunohistochem & Flow Cytometry, Dept Canc Biol, Ahmadabad 380016, Gujarat, India
[2] Gujarat Canc Res Inst, Dept Pathol, Ahmadabad 380016, Gujarat, India
关键词
Cytokeratin; Vimentin; Breast cancer; EPITHELIAL-MESENCHYMAL TRANSITION; ESTROGEN-RECEPTOR; CELL-LINES; INVASIVENESS; ASSOCIATION; CARCINOMA; PHENOTYPE; GROWTH;
D O I
10.1177/172460080902400106
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The transition from epithelial keratin to mesenchymal vimentin expression marks an important step in the malignant progression of breast cancer. This study analyzed the clinical significance of cytokeratin and vimentin in patients with breast cancer. Materials and methods: Expression of cytokeratin and vimentin was evaluated by immunohistochemistry on paraffin-embedded tissue sections of patients with breast cancer. Results: Loss of cytokeratin was seen in 11% of the patients. A clearer trend towards loss of cytokeratin was observed in patients with stage IV disease and PR negativity. Weak cytokeratin expression was present in patients who developed recurrence or metastatic disease. Loss of cytokeratin was associated with reduced overall survival in univariate and multivariate analysis, gain of vimentin expression was seen in 57% of breast carcinoma patients. It was higher in patients with lymph node positivity, advanced stage, HER2 positivity, and disease recurrence or metastasis. Multivariate survival analysis indicated that gain of vimentin expression was associated with reduced relapse-free survival. Conclusion: Loss of cytokeratin and gain of vimentin expression are indicators of biologically aggressive breast carcinoma. (Int J Biol Markers 2009; 24: 38-46)
引用
收藏
页码:38 / 46
页数:9
相关论文
共 21 条
[1]   Cancer and the chemokine network [J].
Balkwill, F .
NATURE REVIEWS CANCER, 2004, 4 (07) :540-550
[2]  
DOMAGALA W, 1990, AM J PATHOL, V136, P219
[3]  
EGER A, 2005, DRUG DISCOVERY TODAY
[4]  
Fuchs IB, 2002, ANTICANCER RES, V22, P3415
[5]   Diverse cellular and molecular mechanisms contribute to epithelial plasticity and metastasis [J].
Grünert, S ;
Jechlinger, M ;
Beug, H .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (08) :657-665
[6]   Epithelial-mesenchymal transition and tumour invasion [J].
Guarino, Marcello .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2007, 39 (12) :2153-2160
[7]   The role of epithelial-mesenchymal transition in cancer pathology [J].
Guarino, Marcello ;
Rubino, Barbara ;
Ballabio, Gianmario .
PATHOLOGY, 2007, 39 (03) :305-318
[8]   Epithelial-mesenchymal transition and its implications for fibrosis [J].
Kalluri, R ;
Neilson, EG .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (12) :1776-1784
[9]   Epithelial-mesenchymal transition in development and cancer:: role of phosphatidylinositol 3′ kinase/AKT pathways [J].
Larue, L ;
Bellacosa, A .
ONCOGENE, 2005, 24 (50) :7443-7454
[10]  
LEE JM, 2005, CANCER RES, V65, P5991