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- BookPhilipp Y. Maximov, Russell E. McDaniel, V. Craig Jordan.Summary: Tamoxifen is a pioneering medicine for the treatment and prevention of breast cancer. It is the first drug targeted therapy in cancer to be successful. Tamoxifen targets the tumor estrogen receptor. The therapy is known to have saved the lives of millions of women over the past 40 years. This monograph, written by V. Craig Jordan - known as the "father of tamoxifen" - and his Tamoxifen Team at the Georgetown University Washington DC, illustrates the journey of this milestone in medicine. It includes a personal interview with V. Craig Jordan about his four decades of discovery in breast cancer research and treatment. V. Craig Jordan was there for the birth of tamoxifen as he is credited for reinventing a "failed morning after contraceptive" to become the "gold standard" for the treatment of breast cancer. He contributed to every aspect of tamoxifen application in therapeutics and all aspects of tamoxifen's pharmacology. He discovered the selective estrogen receptor modulators (SERMs) and explored the new biology of estrogen-induced apoptosis.
Contents:
Discovery and Pharmacology of Nonsteroidal Estrogens and Antiestrogens
Tamoxifen Goes Forward Alone
Metabolites of Tamoxifen as the Basis of Drug Development
Adjuvant Therapy: The Breakthrough
The Wisconsin Story in the 1980s: Discovery of Target Site-Specific Estrogen Action
Carcinogenesis and Tamoxifen
Chemoprevention: Cinderella Waiting for the Ball
Tamoxifen and Raloxifene Head to Head: The STAR Trial
Acquired Resistance to Tamoxifen: Back to the Beginning
The Legacy of Tamoxifen.Digital Access Springer 2013 - ArticleGötze H, Rothman SS.Biochim Biophys Acta. 1978 Sep 11;512(1):214-20.Amylase transport was measured across the rabbit ileum in vitro employing a modified Ussing chamber. Amylase was moved preferentially in the mucosal to serosal direction. Its rate of transfer was 2--3 orders of magnitude greater than that for inulin. Mucosal to serosal transport of exogenous amylase was completely inhibited in the absence of oxygen. There was also a constant release of endogenous amylase from intestinal tissue into both mucosal and serosal compartments in the absence of an exogenous source. An estimate of the rate of amylase absorption indicates that it may be of sufficient magnitude to account for the enteropancreatic circulation of amylase secreted by the pancreas during augmented secretion.