OBJECTIVE: To clarify the role of epidermal growth factor receptor (EGFR) promoter methylation in primary colorectal cancers and corresponding metastases and its relationship to EGFR expression. STUDY DESIGN: Formalin-fixed tumor samples (primary site and metastasis) from colorectal cancer patients were analyzed for EGFR promoter methylation and EGFR immunohistochemistry expression. RESULTS: Among the 63 assessable patients, 25 cases (39.7%) showed EGFR promoter methylation. Forty-two primary colorectal tumors and corresponding metastases were available for paired analysis of EGFR methylation status. EGFR methylation status of the primary tumor was in accordance with that of metastasis in 29 patients (69%). In contrast, 7 patients (50%) with EGFR promoter methylation in the primary tumor showed unmethylated EGFR in metastasis, and 6 metastases (46%) showed EGFR promoter hypermethylation derived from unmethylated EGFR primary tumors. Lack of EGFR protein expression was observed in 8 EGFR promoter methylated primary tumors (44%) and in 7 EGFR promoter methylated metastatic sites (44%). CONCLUSION: EGFR promoter hypermethylation does not seem to represent a rare event in colorectal cancer and may be present differently in different tumor sites. These findings may be relevant to further studies investigating the role of EGFR in colorectal cancer patients. (Anal Quant Cytol Histol 2009;31:417-423)

Epidermal growth factor receptor gene promoter methylation in primary colorectal tumors and corresponding metastatic sites : a new perspective for an "old" therapeutic target / M. Scartozzi, I. Bearzi, A. Mandolesi, E. Galizia, C. Pierantoni, F. Loupakis, R. Berardi, A. Zaniboni, A. Quadri, F. Zorzi, S. Biagetti, C. Loretelli, T. Biscotti, R. Labianca, G. Masi, A. Falcone, S. Cascinu. - In: ANALYTICAL AND QUANTITATIVE CYTOLOGY AND HISTOLOGY. - ISSN 0884-6812. - 31:6(2009 Dec), pp. 417-423.

Epidermal growth factor receptor gene promoter methylation in primary colorectal tumors and corresponding metastatic sites : a new perspective for an "old" therapeutic target

C. Loretelli;
2009

Abstract

OBJECTIVE: To clarify the role of epidermal growth factor receptor (EGFR) promoter methylation in primary colorectal cancers and corresponding metastases and its relationship to EGFR expression. STUDY DESIGN: Formalin-fixed tumor samples (primary site and metastasis) from colorectal cancer patients were analyzed for EGFR promoter methylation and EGFR immunohistochemistry expression. RESULTS: Among the 63 assessable patients, 25 cases (39.7%) showed EGFR promoter methylation. Forty-two primary colorectal tumors and corresponding metastases were available for paired analysis of EGFR methylation status. EGFR methylation status of the primary tumor was in accordance with that of metastasis in 29 patients (69%). In contrast, 7 patients (50%) with EGFR promoter methylation in the primary tumor showed unmethylated EGFR in metastasis, and 6 metastases (46%) showed EGFR promoter hypermethylation derived from unmethylated EGFR primary tumors. Lack of EGFR protein expression was observed in 8 EGFR promoter methylated primary tumors (44%) and in 7 EGFR promoter methylated metastatic sites (44%). CONCLUSION: EGFR promoter hypermethylation does not seem to represent a rare event in colorectal cancer and may be present differently in different tumor sites. These findings may be relevant to further studies investigating the role of EGFR in colorectal cancer patients. (Anal Quant Cytol Histol 2009;31:417-423)
adenocarcinoma; adult; aged; aged, 80 and over; biomarkers, tumor; colorectal neoplasms; female; gene expression regulation, neoplastic; gene silencing; humans; immunohistochemistry; male; middle aged; receptor, epidermal growth factor; DNA methylation; promoter regions, genetic
Settore MED/06 - Oncologia Medica
Settore MED/04 - Patologia Generale
Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica
Settore BIO/13 - Biologia Applicata
Settore MED/03 - Genetica Medica
dic-2009
http://www.aqch.com/toc/auto_abstract.php?id=23055
Article (author)
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/570279
Citazioni
  • ???jsp.display-item.citation.pmc??? 2
  • Scopus 3
  • ???jsp.display-item.citation.isi??? 3
social impact