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Aldosterone-Producing Cell Clusters in Normal and Pathological States.
Omata, Kei; Tomlins, Scott A; Rainey, William E.
Afiliação
  • Omata K; Department of Pathology, University of Michigan, Ann Arbor, MI, USA.
  • Tomlins SA; Division of Nephrology, Endocrinology and Vascular Medicine, Tohoku University, Aoba-ku, Sendai, Miyagi, Japan.
  • Rainey WE; Division of Clinical Hypertension, Endocrinology & Metabolism, Tohoku University, Aoba-ku, Sendai, Miyagi, Japan.
Horm Metab Res ; 49(12): 951-956, 2017 Dec.
Article em En | MEDLINE | ID: mdl-29202494
ABSTRACT
Primary aldosteronism (PA) significantly increases the risk of cardiovascular complications, and early diagnosis and targeted treatment based on its pathophysiology is warranted. Next-generation sequencing (NGS) has revealed recurrent somatic mutations in aldosterone-driving genes in aldosterone-producing adenoma (APA). By applying CYP11B2 (aldosterone synthase) immunohistochemistry and NGS to adrenal glands from normal subjects and PA patients, we and others have shown that CYP11B2-positive cells make small clusters, termed aldosterone-producing cell clusters (APCC), beneath the adrenal capsule, and that APCC harbor somatic mutations in genes mutated in APA. We have shown that APCC are increased in CT-negative PA adrenals, while others showed potential progression from APCC to micro APA through mutations. These results suggest that APCC are a key factor for understanding the origin of PA, and further investigation on the relation between APCC and PA is highly needed.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Adenoma / Neoplasias do Córtex Suprarrenal / Glândulas Suprarrenais / Aldosterona / Hiperaldosteronismo Tipo de estudo: Screening_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Adenoma / Neoplasias do Córtex Suprarrenal / Glândulas Suprarrenais / Aldosterona / Hiperaldosteronismo Tipo de estudo: Screening_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article