Filipe M I, Sandey A, Ma J
Department of Histopathology, United Medical School of Guy's Hospital, London Bridge, England.
Hum Pathol. 1988 Jun;19(6):671-81. doi: 10.1016/s0046-8177(88)80173-4.
The expression of two intestinal mucin-associated antigens large intestine mucin antigen (LIMA) and small intestine mucin antigen (SIMA) were investigated by indirect immunoperoxidase staining of rectal mucosa from patients suffering from ulcerative colitis with (n = 6) and without (n = 31) associated carcinoma and in noncolitic controls (n = 40). The aim was to assess the relationship between antigen patterns and malignant change. SIMA, which is localised predominantly in the small intestine, is virtually undetectable in the normal adult colonic mucosa. However, this antigen is present in the foetal colon and colonic carcinoma. LIMA is expressed in normal colonic mucosa, but absent from the small intestine. LIMA staining patterns were not significantly different among the three groups. In contrast, expression of SIMA was significantly higher in the patients who had developed carcinoma (6/6) than in the noncancer group (7/71) (P less than 0.001). The presence of SIMA was also significantly related to areas of dysplasia compared to normal (P = .03) or inflammation (P less than .05), but it did not differ from mucosa showing "indefinite" atypia. The finding of 31% SIMA-positive biopsies associated with severe inflammation in colitis with active disease, but no evidence of malignancy, is difficult to explain at the present stage. A followup study would be necessary to determine its significance. Perhaps the most important finding is the increased frequency of SIMA-positive foci in histologically normal mucosa in carcinoma patients compared with the noncancer group (P less than .001), suggesting a field change. These observations may be prove useful for the identification of patients who may be at risk of developing carcinoma.
通过间接免疫过氧化物酶染色法,对患有(n = 6)和未患有(n = 31)相关癌的溃疡性结肠炎患者以及非结肠炎对照者(n = 40)的直肠黏膜进行研究,以探究两种肠道黏蛋白相关抗原——大肠黏蛋白抗原(LIMA)和小肠黏蛋白抗原(SIMA)的表达情况。目的是评估抗原模式与恶性变化之间的关系。SIMA主要定位于小肠,在正常成人结肠黏膜中几乎检测不到。然而,这种抗原存在于胎儿结肠和结肠癌中。LIMA在正常结肠黏膜中表达,但在小肠中不存在。三组之间LIMA染色模式无显著差异。相比之下,发生癌症的患者(6/6)中SIMA的表达明显高于非癌症组(7/71)(P小于0.001)。与正常(P = 0.03)或炎症(P小于0.05)相比,SIMA的存在也与发育异常区域显著相关,但与显示“不确定”异型性的黏膜无差异。在患有活动性疾病的结肠炎且无恶性证据的严重炎症相关的活检中,发现31%的活检SIMA呈阳性,这在现阶段难以解释。有必要进行后续研究以确定其意义。也许最重要的发现是,与非癌症组相比,癌症患者组织学正常黏膜中SIMA阳性灶的频率增加(P小于0.001),提示存在场效应改变。这些观察结果可能有助于识别可能有患癌风险的患者。