Hiort Olaf
Division of Experimental Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, Universität zu Lübeck, Lübeck, Germany.
Endocr Dev. 2013;24:33-40. doi: 10.1159/000342499. Epub 2013 Feb 1.
Androgen insensitivity describes the inability of cells to respond adequately to androgens. The clinical aspects are well characterized and described in the androgen insensitivity syndrome, where underandrogenization occurs despite normal to high levels of androgens. In 46,XY individuals, this is associated with a variable phenotype ranging from completely female to ambiguous genitalia and infertility in males with gynecomastia. Androgen action is facilitated by a single androgen receptor (AR), whose gene is localized on the X chromosome. However, the identification of mutations in the AR gene in patients with androgen insensitivity is variable, and chances are lower the more subtle the phenotype is. Therefore, other currently unknown mechanisms must be hypothesized to lead to the respective phenotype. The AR is a nuclear transcription factor, acting in concert with an array of only partly known cofactors serving as modulators of target gene transcription. The induced transcription pattern is highly tissue and cell specific, and in some tissues may lead to lasting changes of cell programming. Only one regulated gene APOD has currently been identified to serve as a clinical tool for the diagnosis of androgen insensitivity.
雄激素不敏感是指细胞对雄激素无法做出充分反应的情况。其临床特征在雄激素不敏感综合征中有详细描述,在该综合征中,尽管雄激素水平正常至高,但仍会出现雄激素化不足的情况。在46,XY个体中,这与多种表型相关,从完全女性化到生殖器模糊,以及伴有男性乳房发育的男性不育。雄激素作用由单一的雄激素受体(AR)介导,其基因位于X染色体上。然而,在雄激素不敏感患者中,AR基因突变的检出情况不一,表型越不明显,检出几率越低。因此,必须假设存在其他目前未知的机制导致相应的表型。AR是一种核转录因子,与一系列仅部分已知的辅助因子协同作用,这些辅助因子作为靶基因转录的调节因子。诱导的转录模式具有高度的组织和细胞特异性,在某些组织中可能导致细胞编程的持久变化。目前仅确定了一个受调控的基因APOD可作为诊断雄激素不敏感的临床工具。