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AT2 receptor stimulation may halt progression of pheochromocytoma.

Abstract
Two patients with pheochromocytoma are described in whom treatment with a high dose of an angiotensin receptor blocker was associated with cessation of tumor growth as assessed by serial CT scanning and plasma norepinephrine estimation. If the association with drug treatment is causal, the mechanism may be through stimulation of the AT2 receptor consequent upon the elevation of plasma angiotensin II levels induced by AT1 receptor blockade. Similar observations in further patients should lead to a placebo-controlled study in patients with malignant or familial pheochromocytoma, or other tumors found to express the AT2 receptor.
AuthorsMorris J Brown, Isla S Mackenzie, Michael J Ashby, Kottekkattu K Balan, Derek S Appleton
JournalAnnals of the New York Academy of Sciences (Ann N Y Acad Sci) Vol. 1073 Pg. 436-43 (Aug 2006) ISSN: 0077-8923 [Print] United States
PMID17102112 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Angiotensin II Type 1 Receptor Blockers
  • Biphenyl Compounds
  • Receptors, Angiotensin
  • Tetrazoles
  • Irbesartan
Topics
  • Adrenal Gland Neoplasms (drug therapy, pathology)
  • Adult
  • Angiotensin II Type 1 Receptor Blockers (pharmacology, therapeutic use)
  • Biphenyl Compounds (pharmacology, therapeutic use)
  • Disease Progression
  • Humans
  • Irbesartan
  • Male
  • Middle Aged
  • Pheochromocytoma (drug therapy, pathology)
  • Receptors, Angiotensin (agonists)
  • Tetrazoles (pharmacology, therapeutic use)
  • Tomography, X-Ray Computed

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