Mucin gene and antigen expression in biliopancreatic carcinogenesis

被引:32
作者
Kim, YS
Gum, JR
Crawley, SC
Deng, G
Ho, JJL
机构
[1] Dept Vet Affairs Med Ctr, Gastrointestinal Res Lab 151M2, San Francisco, CA 94121 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[3] Univ Calif San Francisco, Dept Pathol, San Francisco, CA USA
[4] Univ Calif San Francisco, Dept Anat, San Francisco, CA USA
关键词
carcinogenesis; mucin antigen; mucin gene;
D O I
10.1023/A:1008332602541
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mucins are high molecular weight glycoproteins which are heavily glycosylated with many carbohydrate side chains. In epithelial cancers such as biliopancreatic cancer, both quantitative and qualitative alterations in carbohydrate and polypeptide moieties of mucin glycoproteins occur. These changes in mucin glycoproteins are one of the most common phenotypic markers of biliopancreatic carcinogenesis and may play an important pathobiological role. The expression of some of the sialylated carbohydrate antigens appears to correlate with a poor prognosis and increased metastatic potential in biliopancreatic cancer. The increased exposure of peptide epitopes of mucin glycoproteins in biliopancreatic cancer appears to be due to either abnormal glycosylation and/or altered levels of mucin gene transcription. In addition, dysregulation of tissue specific mucin gene expression occurs in biliopancreatic cancer. This information is currently being exploited for further elucidation of the molecular mechanisms involved in carcinogenesis, tumor progression and metastasis, and the development of novel methods of diagnosis and therapy of biliopancreatic cancer.
引用
收藏
页码:51 / 55
页数:5
相关论文
共 33 条
[1]   ALTERED EXPRESSION OF MUC2, MUC4, AND MUC5 MUCIN GENES IN PANCREAS TISSUES AND CANCER CELL-LINES [J].
BALAGUE, C ;
GAMBUS, G ;
CARRATO, C ;
PORCHET, N ;
AUBERT, JP ;
KIM, YS ;
REAL, FX .
GASTROENTEROLOGY, 1994, 106 (04) :1054-1061
[2]   Enhanced sialylation of mucin-associated carbohydrate structures in human colon cancer metastasis [J].
Bresalier, RS ;
Ho, SB ;
Schoeppner, HL ;
Kim, YS ;
Sleisenger, MH ;
Brodt, P ;
Byrd, JC .
GASTROENTEROLOGY, 1996, 110 (05) :1354-1367
[3]  
CARRAWAY CAC, 1998, 5 INT WORKSH CARC AS
[4]  
CARRAWAY KL, 1998, 5 INT WORKSH CARC AS
[5]   LOCALIZATION OF MUCIN (MUC2 AND MUC3) MESSENGER-RNA AND PEPTIDE EXPRESSION IN HUMAN NORMAL INTESTINE AND COLON-CANCER [J].
CHANG, SK ;
DOHRMAN, AF ;
BASBAUM, CB ;
HO, SB ;
TSUDA, T ;
TORIBARA, NW ;
GUM, JR ;
KIM, YS .
GASTROENTEROLOGY, 1994, 107 (01) :28-36
[6]   Breast cancer selective gene expression and therapy mediated by recombinant adenoviruses containing the DF3/MUC1 promoter [J].
Chen, L ;
Chen, DS ;
Manome, Y ;
Dong, YH ;
Fine, HA ;
Kufe, DW .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (06) :2775-2782
[7]  
CHUNG YS, 1987, CANCER, V60, P1636, DOI 10.1002/1097-0142(19871001)60:7<1636::AID-CNCR2820600736>3.0.CO
[8]  
2-C
[9]   Radioimmunodetection with In-111-labeled monoclonal antibody Nd2 in patients with pancreatic cancer [J].
Chung, YS ;
Sawada, T ;
Kondo, Y ;
Hirayama, K ;
Inui, A ;
Yamashita, Y ;
Nakata, B ;
Okamura, T ;
Ochi, H ;
Ho, JJL ;
Kim, YS ;
Sowa, M .
JAPANESE JOURNAL OF CANCER RESEARCH, 1997, 88 (04) :427-434
[10]   MUC3 human intestinal mucin - Analysis of gene structure, the carboxyl terminus, and a novel upstream repetitive region [J].
Gum, JR ;
Ho, JJL ;
Pratt, WS ;
Hicks, JW ;
Hill, AS ;
Vinall, LE ;
Roberton, AM ;
Swallow, DM ;
Kim, YS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (42) :26678-26686