The Coffey Lecture: steroidogenic enzyme inhibitors and hormone dependent cancer.

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TitleThe Coffey Lecture: steroidogenic enzyme inhibitors and hormone dependent cancer.
Publication TypeJournal Article
Year of Publication2009
AuthorsBrodie, A, Njar, VCO, Macedo, LFurtado, T Vasaitis, S, Sabnis, G
JournalUrol Oncol
Volume27
Issue1
Pagination53-63
Date Published2009 Jan-Feb
ISSN1078-1439
KeywordsAnimals, Antibodies, Monoclonal, Antibodies, Monoclonal, Humanized, Aromatase, Aromatase Inhibitors, Breast Neoplasms, Disease Models, Animal, Enzyme Inhibitors, Female, Humans, Male, Mice, Nitriles, Receptor, erbB-2, Receptors, Estrogen, Steroids, Triazoles
Abstract

OBJECTIVES: To improve treatment for patients with breast and prostate cancer.

METHODS: A number of novel inhibitors of steroidogenic enzymes have been developed. Their biological effects have been evaluated in a variety of preclinical models. Aromatase (estrogen synthetase) inhibitors have now been extensively tested in clinical trials in breast cancer patients. Inhibitors of 17alpha-hydroxylase/lyase have also been studied in preclinical models and are beginning trials in prostate cancer patients.

RESULTS: The enzyme aromatase (CYP19) has proven to be an important therapeutic target. Inhibitors of aromatase (AIs) are showing greater benefit than antiestrogens in the treatment of breast cancer. Although effective in other conditions in both women and men, AIs have not been useful in benign prostatic hypertrophy or prostate cancer. However inhibitors of 17alphahydroxylase/lyase (CYP17) to block synthesis of androgens may be effective for prostate cancer. Recent clinical trials with abiraterone and preclinical studies with other novel CYP17 inhibitors, which also interact with the androgen receptor and cause its down-regulation, could provide a new approach for treating this disease. In further studies, we optimized treatment with aromatase inhibitors and antiestrogens utilizing an intratumoral aromatase xenograft model. AIs were more effective and sustained growth inhibition was longer than antiestrogens. However, inevitably tumors eventually began to grow despite continued treatment. Analysis of breast tumors from mice treated with letrozole revealed up-regulation of HER-2 and MAP Kinase signaling proteins and down-regulation of the estrogen receptor. Our studies showed that tumors adapt to AI treatment by activating alternate signaling pathways, thus enabling them to proliferate in the absence of estrogen. When mice bearing resistant tumors were treated with trastuzumab, the anti-HER-2 antibody (herceptin), HER-2 was decreased in the tumor but the estrogen receptor and aromatase were restored. Tumor growth was significantly inhibited by treatment with trastuzumab in addition to letrozole.

CONCLUSIONS: Aromatase inhibitors are proving to be an effective new class of agents for the treatment of breast cancer. Compounds inhibiting 17alphahydroxylase/lyase have potential for the treatment of prostate cancer. Our results suggest that strategies to overcome resistance to these types of agents can restore sensitivity of the tumors to hormone therapy.

DOI10.1016/j.urolonc.2008.07.036
Alternate JournalUrol. Oncol.
PubMed ID19111799
PubMed Central IDPMC3090255
Grant ListCA-62483 / CA / NCI NIH HHS / United States
R01 CA027440-23 / CA / NCI NIH HHS / United States
R01 CA062483-28W1 / CA / NCI NIH HHS / United States