Loeper Siobhan, Ezzat Shereen
Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Rev Endocr Metab Disord. 2008 Mar;9(1):41-58. doi: 10.1007/s11154-007-9063-z.
Acromegaly is characterized by sustained elevation of circulating growth hormone (GH) and insulin-like growth factor I (IGF-I), and is clearly associated with increased morbidity and overall mortality mainly due to cardiovascular, metabolic, and respiratory diseases. Although cancer-related mortality varies widely amongst retroperspective studies, it appears to be consistently elevated mainly in patients with uncontrolled disease. We review individual tumor types including neoplasms of the colon, breast, prostate, and thyroid where in vitro, animal studies, and studies in non-acromegalic cancer patients have established a role for the GH/IGF-I axis in tumor progression and possibly initiation. We highlight deficiencies in data in acromegalic patients where the evidence is less convincing. Instead, we explore the hypothesis that acromegaly, independent of hormone secretion, is a disease that heralds genetic and/or epigenetic alterations predisposing to cancer risk elsewhere.
肢端肥大症的特征是循环生长激素(GH)和胰岛素样生长因子I(IGF-I)持续升高,并且明显与发病率增加和总体死亡率升高相关,主要原因是心血管、代谢和呼吸系统疾病。尽管在回顾性研究中,癌症相关死亡率差异很大,但似乎主要在疾病未得到控制的患者中持续升高。我们综述了包括结肠、乳腺、前列腺和甲状腺肿瘤在内的各种肿瘤类型,在这些肿瘤类型中,体外研究、动物研究以及对非肢端肥大症癌症患者的研究已经证实生长激素/胰岛素样生长因子I轴在肿瘤进展以及可能的肿瘤发生中发挥作用。我们强调了肢端肥大症患者数据中的不足之处,在这些患者中证据不太令人信服。相反,我们探讨了这样一种假说,即肢端肥大症独立于激素分泌,是一种预示着存在易患其他部位癌症风险的遗传和/或表观遗传改变的疾病。