Chapter

The role of aromatase and other oestrogen producing enzymes in mammary carcinogenesis

06/2007; DOI:10.1007/978-1-4020-5867-7_8 pp.151-170

ABSTRACT There is a large and compelling body of epidemiological and experimental evidence that oestrogens are the fuel behind the
aetiology of breast cancer. The local biosynthesis of oestrogens especially in postmenopausal women as a result of the interactions
of various enzymes is believed to play a very important role in the pathogenesis and development of hormone-dependent breast
carcinoma. The over-expression of such enzymes seems to be associated ciated with the development of a more aggressive disease
and associated with poor outcome and increased local and distant recurrences. In this chapter we shed light on CYP19 gene
expression, aromatase enzyme activity and its role in mammary carcinogenesis. In addition, other oestrogen producing enzymes
such as 17beta hydroxysteroid dehydrogenase 1, 2 and steroid sulphatase and their role in breast cancer development are these
enzymes is crucial to the development of new endocrine preventative and therapeutic strategies in postmenopausal females with
hormonedependant breast cancer. Currently, the third generation of aromatase dependant breast cancer. Currently, the third
generation of aromatase inhibitors has revolutionised the treatment of oestrogen-dependant breast cancer. However, the important
role of both STS and 17beta HSD type 1 therapy. Such endocrine therapy is currently being explored and the development of
STS inhibitors and 17beta HSD 1 inhibitors is underway with promising initial results.

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Keywords

17beta HSD 1 inhibitors
 
17beta HSD type 1 therapy
 
17beta hydroxysteroid dehydrogenase 1
 
aromatase dependant breast cancer
 
aromatase enzyme activity
 
aromatase inhibitors
 
breast cancer development
 
endocrine therapy
 
enzymes
 
hormonedependant breast cancer
 
mammary carcinogenesis
 
new endocrine preventative
 
oestrogen-dependant breast cancer
 
pathogenesis
 
poor outcome
 
postmenopausal women
 
promising initial results
 
STS inhibitors
 
therapeutic strategies
 
various enzymes
 

Mohamed Salhab