Blomain Erik S, Pattison Amanda M, Waldman Scott A
a Department of Pharmacology and Experimental Therapeutics , Thomas Jefferson University , Philadelphia , PA , USA.
Cancer Biol Ther. 2016 Jul 2;17(7):713-8. doi: 10.1080/15384047.2016.1178429. Epub 2016 Apr 22.
Despite advances in screening and prevention strategies, colorectal cancer (CRC) remains the second-leading cause of cancer-related death in the United States. Given this continued public health burden of CRC, there is a clear need for improved disease prevention. CRC initiates and progresses over decades, canonically proceeding via a series of stepwise molecular events that turn a normal epithelium into a dysfunctional epithelium, then subsequently into an adenoma, and finally an invasive adenocarcinoma. An emerging paradigm suggests that guanylyl cyclase C (GUCY2C) functions as a tumor suppressor in the intestine, and that the loss of hormone ligands for this receptor causes epithelial dysfunction and represents an important step in the disease process. In that context, GUCY2C ligand replacement therapy has been proposed as a strategy to prevent colorectal cancer, a translational opportunity that is underscored by the recent regulatory approval of the oral GUCY2C ligand linaclotide (Linzess™, Forest Laboratories and Ironwood Pharmaceuticals, Inc.).
尽管在筛查和预防策略方面取得了进展,但结直肠癌(CRC)在美国仍然是癌症相关死亡的第二大原因。鉴于CRC持续给公众健康带来负担,显然需要改进疾病预防措施。CRC的发生和发展历经数十年,通常通过一系列逐步的分子事件进行,这些事件将正常上皮细胞转变为功能失调的上皮细胞,随后发展为腺瘤,最终成为浸润性腺癌。一种新出现的模式表明,鸟苷酸环化酶C(GUCY2C)在肠道中起肿瘤抑制作用,该受体激素配体的缺失会导致上皮功能障碍,并且是疾病进程中的一个重要步骤。在这种背景下,GUCY2C配体替代疗法已被提议作为预防结直肠癌 的一种策略,口服GUCY2C配体利那洛肽(Linzess™,Forest Laboratories和Ironwood Pharmaceuticals公司)最近获得监管批准,凸显了这一转化医学机遇。