Jass J R, Smith M
Department of Pathology, University of Auckland School of Medicine, New Zealand.
Pathology. 1992 Oct;24(4):233-42. doi: 10.3109/00313029209068874.
Loss of O-acetyl substituents from sialic acid expressed in mucin secreted by hyperplastic polyps (21), adenomas (9), a mixed polyp (1) and adenocarcinomas (41) of the colorectum was investigated by mucin histochemistry (diastase PAS and mild PAS) and by lectin histochemistry (Arachis hypogaea or peanut agglutinin) with (nPNA) and without (PNA) prior neuraminidase digestion. Mild PAS and nPNA reactivity were closely correlated, indicating that loss of O-acetyl substituents at C7, C8 and C9 (hence mild PAS positive) and at C4 (hence neuraminidase labile) occur pari passu. These sialic acid alterations were characteristic of mucin secreted by both adenocarcinoma and hyperplastic polyp. The same changes occurred patchily or focally in adenoma. Five "serrated" adenocarcinomas resembled the hyperplastic polyp both morphologically and histochemically. Luminal secretions within cancers were classified as mucin-like (type I) and non-mucin-like (type II). Mild PAS was the most specific technique for mucin-like intraluminal material. However, accumulated luminal secretions (type I or II) and intracytoplasmic lumina were quite specific features of colorectal cancer and could be effectively highlighted by means of dPAS. PNA reactivity without prior neuraminidase digestion showed a distribution unlike nPNA. Whilst PNA expression was more cancer specific than either mPAS or nPNA, it was observed mainly in cancers secreting little or no mucus, thus limiting its value as a tumor marker.
通过黏蛋白组织化学(淀粉酶PAS和轻度PAS)以及凝集素组织化学(花生凝集素),在有(nPNA)和无(PNA)预先神经氨酸酶消化的情况下,研究了大肠增生性息肉(21例)、腺瘤(9例)、混合性息肉(1例)和腺癌(41例)所分泌黏蛋白中唾液酸O - 乙酰取代基的缺失情况。轻度PAS和nPNA反应密切相关,表明C7、C8和C9位(因此轻度PAS阳性)以及C4位(因此对神经氨酸酶敏感)的O - 乙酰取代基缺失同时发生。这些唾液酸改变是腺癌和增生性息肉所分泌黏蛋白的特征。同样的变化在腺瘤中呈散在或局灶性出现。5例“锯齿状”腺癌在形态学和组织化学上与增生性息肉相似。癌腔内的分泌物分为黏蛋白样(I型)和非黏蛋白样(II型)。轻度PAS是检测黏蛋白样腔内物质最特异的技术。然而,积聚的腔内分泌物(I型或II型)和胞质内腔是结直肠癌相当特异的特征,可通过dPAS有效突显。未经预先神经氨酸酶消化的PNA反应显示出与nPNA不同的分布。虽然PNA表达比mPAS或nPNA更具癌症特异性,但主要在分泌很少或不分泌黏液的癌症中观察到,因此限制了其作为肿瘤标志物的价值。