RNA Expression of Cytochrome P450 in Breast Cancer Patients
Background: The expression pattern of cytochrome P450 genes (CYPs) affected by tumorigenesis may have an important role in the progression of cancer and in the metabolism of anticancer drugs. The aim of the study was to determine the expression patterns of four cytochrome P450 genes (CYP1B1, 2C9, 2E...
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Published in | Anticancer research Vol. 27; no. 6C; pp. 4443 - 4450 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Attiki
International Institute of Anticancer Research
01.11.2007
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Subjects | |
Online Access | Get full text |
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Summary: | Background: The expression pattern of cytochrome P450 genes (CYPs) affected by tumorigenesis may have an important role in
the progression of cancer and in the metabolism of anticancer drugs. The aim of the study was to determine the expression
patterns of four cytochrome P450 genes (CYP1B1, 2C9, 2E1 and 3A4) in breast cancer patients. Patients and Methods: mRNA expression
was quantified by real-time PCR. Analyses of 40 sets of human breast tumors, adjacent non-tumor tissues and of 18 peripheral
blood lymphocyte samples were performed. Expression levels were tested for correlation with clinical and pathological data
of patients. Results: Expression levels of CYP2C9 and CYP3A4 were negligible. CYP1B1 expression was on average 50-fold higher
than that of CYP2E1 with overexpression detected in one third of the tumors. Correlation of CYP1B1 expression in lymphocytes
with that in non-tumor tissues was found. Significantly higher CYP2E1 expression was associated with an invasive lobular type
of tumor, locally advanced disease as well as with non-tumor tissue of progesterone receptor-negative patients. Conclusion:
CYP2E1 expression has a potential role as a breast cancer prognosis marker. The observed high CYP1B1 expression in tumor cells
may evoke changes in their response to drugs which are substrates of P450 1B1 and influence metabolism or activation of environmental
carcinogens. |
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ISSN: | 0250-7005 1791-7530 |