Breast cancer nodal metastasis correlates with tumour and lymph node methylation profiles of Caveolin-1 and CXCR4

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3088294 62 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Breast cancer nodal metastasis correlates with tumour and lymph node methylation profiles of Caveolin-1 and CXCR4
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
DNA methylation is the best characterised epigenetic change so far. However, its role in breast cancer metastasis has not as yet been elucidated. The aim of this study was to investigate the differences between the methylation profiles characterising primary tumours and their corresponding positive or negative for metastasis lymph nodes (LN) and correlate these with tumour metastatic potential. Methylation signatures of Caveolin-1, CXCR4, RAR-β, Cyclin D2 and Twist gene promoters were studied in 30 breast cancer primary lesions and their corresponding metastasis-free and tumour-infiltrated LN with Methylation-Specific PCR. CXCR4 and Caveolin-1 expression was further studied by immunohistochemistry. Tumours were typified by methylation of RAR-β and hypermethylation of Cyclin-D2 and Twist gene promoters. Tumour patterns were highly conserved in tumour-infiltrated LN. CXCR4 and Caveolin-1 promoter methylation patterns differentiated between node-negative and metastatic tumours. Nodal metastasis was associated with tumour and lymph node profiles of extended methylation of Caveolin-1 and lack of CXCR4 hypermethylation. Immunodetection studies verified CXCR4 and Caveolin-1 hypermethylation as gene silencing mechanism. Absence of Caveolin-1 expression in stromal cells associated with tumour aggressiveness while strong Caveolin-1 expression in tumour cells correlated with decreased 7-year disease-free survival. Methylation-mediated activation of CXCR4 and inactivation of Caveolin-1 was linked with nodal metastasis while intratumoral Caveolin-1 expression heterogeneity correlated with disease progression. This evidence contributes to the better understanding and, thereby, therapeutic management of breast cancer metastasis process. © 2014 Springer Science+Business Media Dordrecht.
Έτος δημοσίευσης:
2014
Συγγραφείς:
Alevizos, L.
Kataki, A.
Derventzi, A.
Gomatos, I.
Loutraris, C.
Gloustianou, G.
Manouras, A.
Konstadoulakis, M.M.
Zografos, G.
Περιοδικό:
Clinical and Experimental Metastasis
Εκδότης:
Kluwer Academic Publishers
Τόμος:
31
Αριθμός / τεύχος:
5
Σελίδες:
511-520
Λέξεις-κλειδιά:
caveolin 1; chemokine receptor CXCR4; cyclin D2; DNA; retinoic acid receptor beta, adult; aged; article; breast cancer; clinical article; controlled study; DNA methylation; DNA sequence; female; human; human tissue; immunohistochemistry; lymph node metastasis; methylation specific polymerase chain reaction; pathologist; polymerase chain reaction; promoter region; protein expression, Adult; Aged; Breast Neoplasms; Caveolin 1; DNA Methylation; Female; Gene Expression Profiling; Humans; Immunophenotyping; Lymph Nodes; Lymphatic Metastasis; Middle Aged; Neoplasm Grading; Neoplasm Staging; Promoter Regions, Genetic; Receptors, CXCR4; Risk Factors
Επίσημο URL (Εκδότης):
DOI:
10.1007/s10585-014-9645-6
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