Nanes M S, Catherwood B D
Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.
Annu Rev Med. 1992;43:253-68. doi: 10.1146/annurev.me.43.020192.001345.
The familial nature of multiple endocrine neoplasia syndromes (FMEN) has been recognized for some time but little is known about their cause. Recent application of new molecular techniques has mapped FMEN syndromes to specific chromosomes and provided evidence for the mechanism through which neoplasia occurs. In this review, we describe the techniques that led to recent advances in our understanding of FMEN and we discuss the evidence supporting proposed molecular mechanisms of neoplasia.
多发性内分泌肿瘤综合征(FMEN)的家族性特征已被认识一段时间了,但对其病因却知之甚少。新分子技术的近期应用已将FMEN综合征定位到特定染色体,并为肿瘤形成的机制提供了证据。在这篇综述中,我们描述了促使我们对FMEN的理解取得近期进展的技术,并讨论了支持所提出的肿瘤形成分子机制的证据。