Immunohistochemical staining patterns of MUC1, MUC2, MUC4, and MUC5AC mucins in hyperplastic polyps, serrated adenomas, and traditional adenomas of the colorectum

被引:123
作者
Biemer-Hüttmann, AE
Walsh, MD
McGuckin, MA
Ajioka, Y
Watanabe, H
Leggett, BA
Jass, JR [1 ]
机构
[1] Univ Queensland, Mayo Med Sch, Dept Pathol, Herston, Qld 4006, Australia
[2] Univ Queensland, Dept Obstet & Gynaecol, Brisbane, Qld, Australia
[3] Niigata Univ, Sch Med, Dept Pathol 1, Niigata, Japan
[4] Royal Brisbane Hosp, Dept Gastroenterol, Brisbane, Qld 4029, Australia
关键词
mucin; MUC1; MUC2; MUC4; MUC5AC; traditional adenoma; hyperplastic polyp; serrated adenoma; colon; neoplastic potential;
D O I
10.1177/002215549904700808
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We studied the distribution of the four human apomucins MUC1, MUC2, MUC4, and MUC5AC in hyperplastic polyps, serrated adenomas, and traditional adenomas of the colorectum using immunohistochemical techniques, with the aim of comparing and contrasting their patterns of expression. A series of 12 hyperplastic polyps, 27 serrated adenomas, and 20 traditional adenomas was studied. No significant change in apomucin expression was observed in traditional adenomas compared with normal colorectal epithelium, except for MUC5AC, which was present in 12 of the adenomas (60%) and only 20% of the normal samples. In both hyperplastic polyps and serrated adenomas, MUC2 and MUC5AC mucin expression was consistently and markedly increased. In 50% of the hyperplastic polyps, MUC4 was reduced but in the remaining cases was similar to normal. Loss of MUC4 expression was observed in all serrated adenomas. MUC1 was not increased in the hyperplastic polyps but increased expression was seen in 17 of the serrated adenomas (63 %). Similar altered distribution patterns of MUC2, MUC4 and MUC5AC were seen in hyperplastic polyps and serrated adenomas, whereas traditional adenomas showed little change from normal patterns of expression. Although hyperplastic polyps are commonly defined as benign lesions without neoplastic potential, the similar phenotypes of hyperplastic and serrated adenomas and the existence of mixed polyps suggest that these lesions may represent a histogenetic continuum.
引用
收藏
页码:1039 / 1047
页数:9
相关论文
共 49 条
[1]   Infrequent K-ras codon 12 mutation in serrated adenomas of human colorectum [J].
Ajioka, Y ;
Watanabe, H ;
Jass, JR ;
Yokota, Y ;
Kobayashi, M ;
Nishikura, K .
GUT, 1998, 42 (05) :680-684
[2]   MUC1 and MUC2 mucins in flat and polypoid colorectal adenomas [J].
Ajioka, Y ;
Watanabe, H ;
Jass, JR .
JOURNAL OF CLINICAL PATHOLOGY, 1997, 50 (05) :417-421
[3]   EXPRESSION OF HUMAN MUCIN GENES IN RESPIRATORY, DIGESTIVE, AND REPRODUCTIVE TRACTS ASCERTAINED BY IN-SITU HYBRIDIZATION [J].
AUDIE, JP ;
JANIN, A ;
PORCHET, N ;
COPIN, MC ;
GOSSELIN, B ;
AUBERT, JP .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1993, 41 (10) :1479-1485
[4]  
Bara J, 1998, INT J CANCER, V75, P767, DOI 10.1002/(SICI)1097-0215(19980302)75:5<767::AID-IJC17>3.0.CO
[5]  
2-3
[6]   EXPRESSION OF MUC2-MUCIN IN COLORECTAL ADENOMAS AND CARCINOMAS OF DIFFERENT HISTOLOGICAL TYPES [J].
BLANK, M ;
KLUSSMANN, E ;
KRUGERKRASAGAKES, S ;
SCHMITTGRAFF, A ;
STOLTE, M ;
BORNHOEFT, G ;
STEIN, H ;
XING, PX ;
MCKENZIE, IFC ;
VERSTIJNEN, CPHJ ;
RIECKEN, EO ;
HANSKI, C .
INTERNATIONAL JOURNAL OF CANCER, 1994, 59 (03) :301-306
[7]   Mucin gene expression in human embryonic and fetal intestine [J].
Buisine, MP ;
Devisme, L ;
Savidge, TC ;
Gespach, C ;
Gosselin, B ;
Porchet, N ;
Aubert, JP .
GUT, 1998, 43 (04) :519-524
[8]   Aberrant expression of a human mucin gene (MUC5AC) in rectosigmoid villous adenoma [J].
Buisine, MP ;
Janin, A ;
Maunoury, V ;
Audie, JP ;
Delescaut, MP ;
Copin, MC ;
Colombel, JF ;
Degand, P ;
Aubert, JP ;
Porchet, N .
GASTROENTEROLOGY, 1996, 110 (01) :84-91
[9]  
CONG NV, 1990, HUM GENET, V86, P167
[10]   ADENOMATOUS AND CARCINOMATOUS CHANGES WITHIN HYPERPLASTIC COLONIC EPITHELIUM [J].
COOPER, HS ;
PATCHEFSKY, AS ;
MARKS, G .
DISEASES OF THE COLON & RECTUM, 1979, 22 (03) :152-156