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  • Approximately one half of newly diagnosed female cancers are hormone-dependent, namely breast, ovarian and endometrial tumours. Female breast cancer incidence varies substantially worldwide with women in North America and Northern Europe at highest risk. On the basis of experimental, epidemiologic and clinical studies, ovarian hormones, estradiol and progesterone, influence normal breast cell growth and development and are therefore strongly implicated in the aetiology of human breast cancer. Particular molecular mechanism of action of both hormones in carcinogenesis is being extensively studied. The originally described pathway includes the classical interaction of ligand-bound oestrogen receptor dimers with oestrogen-responsive elements in promoter region of target genes that promote growth of mammary epithelium. The main downstream mediators of oestrogen action include epidermal growth factor, transforming growth factors alpha and beta, platelet-derived growth factor, insulin–like growth factors I and II. Besides this classical pathway there has been documented non-transcriptional effect of oestrogen which acts through activation of mitogen-activated protein kinases. The role of progesterone in breast cancer is less understood, however progestin stimulation of breast cancer motility and invasion has been demonstrated. Hormone receptor positive breast cancers are very pliable to respond to endocrine therapy and oestrogen and progesterone receptor expression is an important predictor of response to hormonal therapy, which is the most important therapeutic approach in hormone receptor positive breast cancers. However up to half of patients relapse despite adjuvant hormonal therapy and resistance to anti-hormonal drugs unavoidably develops. Identification of resistance mechanism may enable development of new pharmaceutical compounds targeted at key molecules of therapy resistance pathways.
  • Approximately one half of newly diagnosed female cancers are hormone-dependent, namely breast, ovarian and endometrial tumours. Female breast cancer incidence varies substantially worldwide with women in North America and Northern Europe at highest risk. On the basis of experimental, epidemiologic and clinical studies, ovarian hormones, estradiol and progesterone, influence normal breast cell growth and development and are therefore strongly implicated in the aetiology of human breast cancer. Particular molecular mechanism of action of both hormones in carcinogenesis is being extensively studied. The originally described pathway includes the classical interaction of ligand-bound oestrogen receptor dimers with oestrogen-responsive elements in promoter region of target genes that promote growth of mammary epithelium. The main downstream mediators of oestrogen action include epidermal growth factor, transforming growth factors alpha and beta, platelet-derived growth factor, insulin–like growth factors I and II. Besides this classical pathway there has been documented non-transcriptional effect of oestrogen which acts through activation of mitogen-activated protein kinases. The role of progesterone in breast cancer is less understood, however progestin stimulation of breast cancer motility and invasion has been demonstrated. Hormone receptor positive breast cancers are very pliable to respond to endocrine therapy and oestrogen and progesterone receptor expression is an important predictor of response to hormonal therapy, which is the most important therapeutic approach in hormone receptor positive breast cancers. However up to half of patients relapse despite adjuvant hormonal therapy and resistance to anti-hormonal drugs unavoidably develops. Identification of resistance mechanism may enable development of new pharmaceutical compounds targeted at key molecules of therapy resistance pathways. (en)
Title
  • Hormones in breast carcinogenesis
  • Hormones in breast carcinogenesis (en)
skos:prefLabel
  • Hormones in breast carcinogenesis
  • Hormones in breast carcinogenesis (en)
skos:notation
  • RIV/00209805:_____/13:#0000460!RIV14-MSM-00209805
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(ED2.1.00/03.0101)
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
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  • 78052
http://linked.open...ai/riv/idVysledku
  • RIV/00209805:_____/13:#0000460
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • oestrogen; progesterone; hormonal receptor; BRCA1/2; mammary glands (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...ontrolniKodProRIV
  • [F1E2C12BC937]
http://linked.open...i/riv/mistoVydani
  • New York
http://linked.open...i/riv/nazevZdroje
  • Hormones and behavior
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...v/pocetStranKnihy
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...iv/tvurceVysledku
  • Brychtová, Veronika
  • Hrstka, Roman
number of pages
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  • Nova Science Publishers
https://schema.org/isbn
  • 978-1-62417-767-5
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