Novel pathway for somatostatin analogs in patients with acromegaly
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作者:
Gadelha, Monica R.
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Univ Fed Rio de Janeiro, Clementino Fraga Filho Univ Hosp, Div Endocrinol, Rio De Janeiro, BrazilUniv Fed Rio de Janeiro, Clementino Fraga Filho Univ Hosp, Div Endocrinol, Rio De Janeiro, Brazil
Gadelha, Monica R.
[1
]
Kasuki, Leandro
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Univ Fed Rio de Janeiro, Clementino Fraga Filho Univ Hosp, Div Endocrinol, Rio De Janeiro, BrazilUniv Fed Rio de Janeiro, Clementino Fraga Filho Univ Hosp, Div Endocrinol, Rio De Janeiro, Brazil
Kasuki, Leandro
[1
]
Korbonits, Marta
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Queen Mary Univ London, Barts & London Sch Med, Ctr Endocrinol, London EC1A 6BQ, EnglandUniv Fed Rio de Janeiro, Clementino Fraga Filho Univ Hosp, Div Endocrinol, Rio De Janeiro, Brazil
Korbonits, Marta
[2
]
机构:
[1] Univ Fed Rio de Janeiro, Clementino Fraga Filho Univ Hosp, Div Endocrinol, Rio De Janeiro, Brazil
[2] Queen Mary Univ London, Barts & London Sch Med, Ctr Endocrinol, London EC1A 6BQ, England
Acromegaly is a chronic disease with increased morbidity and mortality, where usually multiple treatment modalities are used. The somatostatin analogs (SSAs) are the mainstay of medical therapy but, in many patients, including those with a germline mutation in the aryl hydrocarbon receptor-interacting protein (AIP) gene, disease activity cannot be controlled with these drugs. Previous data have suggested the involvement of the tumor-suppressor gene ZAC1 in the mechanism of action of SSAs, and more recent findings suggested that SSAs could regulate AIP, which in turn can stimulate ZAC1, therefore suggesting the existence of a SSA-AIP-ZAC1 somatostatin effect pathway. The current review discusses these novel observations, highlighting their significance in the treatment of sporadic and familial somatotroph adenomas.