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020 _a9783764374181
040 _aES-MaUEC
050 4 _aRC280.B8
_bA76 2006 EB
245 0 0 _aAromatase Inhibitors
_cedited by Barrington J.A. Furr
260 _aBasel
_bBirkhäuser
_c2006
300 _a1 recurso en línea (IX, 182 p.) 30 il.
336 _aTexto (visual)
_btxt
_2rdacontent
337 _aelectrónico
_bc
_2rdamedia
338 _arecurso electrónico
_bcr
_2rdacarrier
490 1 _aMilestones in Drug Therapy MDT
520 _aMany breast tumours are dependent upon oestrogen for their development and continued growth. Over the last 25 years hormone therapy has progressed from the irreversible destruction of endocrine glands to the use of drugs that reversibly suppress oestrogen synthesis or action. The inhibition of oestrogen synthesis is most readily achieved by inhibiting the final step in the pathway of oestrogen biosynthesis, the reaction which transforms androgens into oestrogens by creating an aromatic ring in the steroid molecule (hence the enzyme's trivial name, aromatase). Whereas the first aromatase inhibitors to be used therapeutically could be shown to produce drug-induced inhibition of the enzyme and therapeutic benefits in patients with breast cancer, they were not particularly potent and lacked specificity. However, second-generation drugs were developed and most recently third-generation inhibitors have evolved which possess remarkable specificity and potency. Initial results from clinical trials suggest that these agents will become the cornerstones of future endocrine therapy
942 _2lcc
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988 _aEBOOK, EBSPRINGERrevisando
650 7 _aMamas
_xCáncer
_0comprobar BNE19901364206
_2embne
_9182522
700 1 _aFurr, Barrington J. A.
_eeditor literario
_0Local
_985759
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/3-7643-7418-7
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
901 _ai9783764374181
907 _a.b12822280
_b10-10-17
_c01-10-14
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_b17-03-17
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