Preston Sean L, Wong Wai-Man, Chan Annie On-On, Poulsom Richard, Jeffery Rosemary, Goodlad Robert A, Mandir Nikki, Elia George, Novelli Marco, Bodmer Walter F, Tomlinson Ian P, Wright Nicholas A
Histopathology Unit, London Research Institute, Cancer Research UK, London WC2A 3PX, United Kingdom.
Cancer Res. 2003 Jul 1;63(13):3819-25.
The adenoma:carcinoma sequence is well established. Understanding the molecular pathology of the adenoma is therefore important. There is great controversy within the field. The Vogelstein group champions the "top-down" theory (colorectal adenomas arise and grow across the mucosal surface and down into the crypts), whereas other studies, including our own, propose "bottom-up" spread. Serial sections of 40 small (<3 mm) sporadic colorectal adenomas were stained with H&E, MIB-1, and for beta-catenin. 10 early adenomas were Feulgen-stained and microdissected. We also examined the flat mucosa of three patients who had undergone colectomies for familial adenomatous polyposis (FAP) and specimens from a XO/XY individual with FAP, the latter using in situ hybridization for the Y chromosome. In the earliest sporadic adenomas, there were crypts entirely filled with adenomatous epithelium, which showed proliferative activity and nuclear localization of beta-catenin. There was a sharp cutoff between crypt epithelial cells showing nuclear beta-catenin and surface cells with membrane staining. In slightly larger lesions, adenomatous spread from above was seen. Microdissected adenomas showed multiple fission events, with proliferation distributed equally throughout. In FAP tissue, numerous isolated monocryptal adenomas, which were clonal in origin, were seen. Examination of adenomas in the XO/XY individual showed no instances of XY or XO adenomatous epithelium growing down into crypts of the other genotype. Both sporadic and FAP adenomas start as a unicryptal adenomas and grow initially by crypt fission--a bottom-up pattern. Later, in sporadic adenomas, there is evidence of growth down into adjacent crypts (top-down).
腺瘤-癌序列已得到充分证实。因此,了解腺瘤的分子病理学很重要。该领域存在很大争议。沃格尔斯坦团队支持“自上而下”理论(结直肠腺瘤在黏膜表面发生并生长,向下延伸至隐窝),而包括我们自己的研究在内的其他研究则提出“自下而上”的扩散方式。对40个小的(<3毫米)散发性结直肠腺瘤的连续切片进行苏木精-伊红染色(H&E)、MIB-1染色以及β-连环蛋白染色。对10个早期腺瘤进行福尔根染色并显微切割。我们还检查了3例因家族性腺瘤性息肉病(FAP)接受结肠切除术患者的扁平黏膜,以及1例患有FAP的XO/XY个体的标本,后者采用Y染色体原位杂交技术。在最早的散发性腺瘤中,存在完全被腺瘤上皮填充的隐窝,这些上皮显示出增殖活性以及β-连环蛋白的核定位。显示核β-连环蛋白的隐窝上皮细胞与膜染色的表面细胞之间有明显界限。在稍大的病变中,可见腺瘤从上方蔓延。显微切割的腺瘤显示出多个裂变事件,增殖均匀分布于各处。在FAP组织中,可见许多起源为克隆性的孤立单隐窝腺瘤。对XO/XY个体的腺瘤检查未发现XY或XO腺瘤上皮向下生长至另一种基因型隐窝的情况。散发性和FAP腺瘤均起始于单隐窝腺瘤,最初通过隐窝裂变生长——一种自下而上的模式。后来,在散发性腺瘤中,有证据表明其向下生长至相邻隐窝(自上而下)。