Andrews C W, Jessup J M, Goldman H, Hayes D F, Kufe D W, O'Hara C J, Steele G D
Department of Pathology, Deaconess Hospital, Harvard Medical School, Boston, Massachusetts 02215.
Cancer. 1993 Dec 1;72(11):3185-90. doi: 10.1002/1097-0142(19931201)72:11<3185::aid-cncr2820721109>3.0.co;2-7.
The expression of DF3 was assessed by a monoclonal antibody in normal, inflammatory, and neoplastic conditions in the large bowel.
Using immunohistochemistry, expression was examined in formalin-fixed paraffin-embedded biopsy and resection samples of 19 normal colonic mucosal specimens, 49 inflammatory lesions, 34 adenomas, and 38 primary colonic adenocarcinomas. In addition, Western blots of normal colonic mucosa and adenocarcinoma were examined.
DF3 expression was detected in 84% of the adenocarcinomas with coarse membrane staining, intense positivity of luminal secretions, and focal cytoplasmic and intracytoplasmic vacuole staining. Nine of 32 areas of transitional mucosa revealed reactivity along apical membranes in crypt cells. Five adenomas containing carcinoma revealed DF3 positivity in the malignant areas only, whereas the remaining 29 were negative. Staining was membrane, luminal, and intracytoplasmic. Two examples of active ulcerative colitis revealed focal reactivity along the apical membrane of crypt cells. No other areas of staining were noted, including 12 cases containing dysplasia. Four of 10 other inflammatory lesions also revealed similar membrane reactivity in crypt cells. Normal colonic mucosa was nonreactive. Examples of normal colonic mucosa were negative for DF3 by Western blot analysis, whereas two carcinoma samples that reacted immunohistochemically were positive.
DF3 is not detectable in normal colonic tissues. It is expressed focally and predominantly along the apical membrane of crypt cells in some inflammatory lesions and in the transitional mucosa of primary adenocarcinomas. Most adenocarcinomas of the colon and adenomas with foci of invasive carcinoma demonstrate reactivity in the cytoplasm and luminal secretions.
采用单克隆抗体评估DF3在大肠正常、炎症及肿瘤状态下的表达情况。
运用免疫组织化学方法,检测19例正常结肠黏膜标本、49例炎症性病变、34例腺瘤以及38例原发性结肠腺癌的福尔马林固定石蜡包埋活检及切除样本中的表达。此外,还对正常结肠黏膜和腺癌进行了蛋白质免疫印迹分析。
在84%的腺癌中检测到DF3表达,表现为粗颗粒状膜染色、管腔分泌物强阳性以及局灶性细胞质和胞质内空泡染色。32个移行黏膜区域中有9个显示隐窝细胞顶端膜有反应性。5例含癌腺瘤仅在恶性区域显示DF3阳性,其余29例为阴性。染色位于膜、管腔及胞质内。2例活动性溃疡性结肠炎显示隐窝细胞顶端膜有局灶性反应性。未发现其他染色区域,包括12例伴有发育异常的病例。10例其他炎症性病变中有4例也显示隐窝细胞有类似的膜反应性。正常结肠黏膜无反应性。正常结肠黏膜样本经蛋白质免疫印迹分析DF3呈阴性,而2例免疫组织化学有反应的癌样本呈阳性。
正常结肠组织中检测不到DF3。在一些炎症性病变及原发性腺癌的移行黏膜中,DF3在隐窝细胞顶端膜呈局灶性且主要表达。大多数结肠腺癌及有浸润癌灶的腺瘤在细胞质和管腔分泌物中显示反应性。