Chen Zong-Ming E, Ritter Jon H, Wang Hanlin L
Lauren V. Ackerman Laboratory of Surgical Pathology, Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110-1093, USA.
Am J Surg Pathol. 2005 Jul;29(7):890-6. doi: 10.1097/01.pas.0000167364.90899.59.
Alpha-methylacyl coenzyme A racemase (AMACR), a novel immunomarker for prostatic adenocarcinoma, has recently been shown to be expressed in a number of malignancies including colorectal adenocarcinoma. In the current study, 59 surgically resected primary small intestinal adenocarcinomas (34 ampullary and 25 non-ampullary) were immunohistochemically examined for AMACR expression and compared with 66 colorectal adenocarcinomas (including 24 secondary tumors involving the small intestine by direct extension or metastasis). The results show that no AMACR immunoreactivity was detected in normal-appearing small and large intestinal mucosa. While 41 of 66 (62%) colorectal adenocarcinomas exhibited a variable degree of cytoplasmic staining, only 1 of 25 (4%) non-ampullary and 2 of 34 (6%) ampullary small intestinal adenocarcinomas showed positive AMACR immunoreactivity (P < 0.0001). Interestingly, AMACR appeared to be less frequently expressed in mucinous or poorly differentiated colorectal adenocarcinomas when compared with non-mucinous or better-differentiated counterparts, suggesting an association with microsatellite instability status. These results extend our previous observations that small intestinal adenocarcinomas differ markedly from colorectal adenocarcinomas despite their morphologic similarity. The different AMACR expression patterns may not only provide an additional diagnostic tool in the distinction between adenocarcinomas of the small and large intestinal origins but may also shed light on further understanding of intestinal tumorigenesis.
α-甲基酰基辅酶A消旋酶(AMACR)是一种用于前列腺腺癌的新型免疫标志物,最近已被证明在包括结肠腺癌在内的多种恶性肿瘤中表达。在本研究中,对59例手术切除的原发性小肠腺癌(34例壶腹周围型和25例非壶腹周围型)进行免疫组织化学检测,以检测AMACR的表达,并与66例结肠腺癌(包括24例通过直接蔓延或转移累及小肠的继发性肿瘤)进行比较。结果显示,在外观正常的小肠和大肠黏膜中未检测到AMACR免疫反应性。虽然66例结肠腺癌中有41例(62%)表现出不同程度的细胞质染色,但25例非壶腹周围型小肠腺癌中只有1例(4%)和34例壶腹周围型小肠腺癌中有2例(6%)显示AMACR免疫反应性阳性(P<0.0001)。有趣的是,与非黏液性或高分化的结肠腺癌相比,AMACR在黏液性或低分化的结肠腺癌中似乎表达频率较低,提示与微卫星不稳定性状态有关。这些结果扩展了我们之前的观察结果,即小肠腺癌尽管形态相似,但与结肠腺癌明显不同。不同的AMACR表达模式不仅可能为区分小肠和大肠来源的腺癌提供一种额外的诊断工具,还可能有助于进一步了解肠道肿瘤发生机制。