Expression profile of mucins (MUC1, MUC2, MUC5AC, and MUC6) in ovarian mucinous tumours: changes in expression from benign to malignant tumours

被引:25
作者
Wang, Jayson [1 ]
El-Bahrawy, Mona [1 ,2 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Histopathol, London W12 0NN, England
[2] Univ Alexandria, Dept Pathol, Alexandria, Egypt
关键词
immunohistochemistry; mucin; ovary; tumorigenesis; tumour; GASTRIC-CARCINOMA; DIAGNOSIS; CANCER; ADENOCARCINOMA; INDUCTION; THERAPY;
D O I
10.1111/his.12578
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
AimsMucins (MUCs) constitute a family of glycoproteins expressed by epithelial cells. They show specific tissue-type expression, and are useful for differentiating between different cancers. Studies have shown changes in MUC expression with tumour progression in a variety of cancers. The aim of this study was to characterize the profile of MUC expression in benign, borderline and malignant intestinal-type ovarian mucinous tumours (OMTs). Methods and resultsMUC1, MUC2, MUC5AC and MUC6 expression was studied by immunohistochemistry in 53 OMTs (19 malignant, 25 borderline, and nine benign). The positivity frequencies of MUC1 in benign, borderline and malignant OMTs were 22.2%, 12%, and 31.6%, respectively. For MUC2, they were 0%, 40%, and 42.1%, respectively. For MUC5AC, they were 100%, 100%, and 94.8%, respectively. For MUC6, they were 66.7%, 16%, and 26.3%, respectively. Significantly increased MUC2 expression and decreased MUC6 expression were seen in borderline and malignant OMTs, as compared with benign tumours. ConclusionThis is the first study to compare the expression of all four MUCs in OMT with statistical analysis. We show that MUC2 expression and MUC6 expression change with the progression of benign to borderline and malignant tumours. We suggest that these changes may contribute to malignant transformation.
引用
收藏
页码:529 / 535
页数:7
相关论文
共 21 条
[1]   Differential expression of MUC2 and MUC5AC mucin genes in primary ovarian and metastatic colonic carcinoma [J].
Albarracin, CT ;
Jafri, J ;
Montag, AG ;
Hart, J ;
Kuan, SF .
HUMAN PATHOLOGY, 2000, 31 (06) :672-677
[2]  
Boman F, 2001, J PATHOL, V193, P339, DOI 10.1002/1096-9896(2000)9999:9999<::AID-PATH798>3.0.CO
[3]  
2-9
[4]  
Burjonrappa S C, 2007, Indian J Cancer, V44, P1
[5]   Mucins in ovarian cancer diagnosis and therapy [J].
Chauhan, Subhash C. ;
Kumar, Deepak ;
Jaggi, Meena .
JOURNAL OF OVARIAN RESEARCH, 2009, 2 (01)
[6]   Determining the Site of Origin of Mucinous Adenocarcinoma: An Immunohistochemical Study of 175 Cases [J].
Chu, Peiguo G. ;
Chung, Lawrence ;
Weiss, Lawrence M. ;
Lau, Sean K. .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2011, 35 (12) :1830-1836
[7]  
Dong Y, 1997, J PATHOL, V183, P311, DOI 10.1002/(SICI)1096-9896(199711)183:3<311::AID-PATH917>3.0.CO
[8]  
2-2
[9]   Expression of MUC1 and MUC2 mucin gene products in human ovarian carcinomas [J].
Feng, H ;
Ghazizadeh, M ;
Konishi, H ;
Araki, T .
JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2002, 32 (12) :525-529
[10]   A phase I trial of a synthetic mucin peptide vaccine induction of specific immune reactivity in patients with adenocarcinoma [J].
Goydos, JS ;
Elder, E ;
Whiteside, TL ;
Finn, OJ ;
Lotze, MT .
JOURNAL OF SURGICAL RESEARCH, 1996, 63 (01) :298-304