Expression of sulfated carbohydrate chain and core peptides of mucin detected by monoclonal antibodies in Barrett's esophagus and esophageal adenocarcinoma

被引:0
|
作者
Takao Endo
Kazuhiro Tamaki
Yoshiaki Arimura
Fumio Itoh
Yuji Hinoda
Masato Hareyama
Tatsuro Irimura
Masahiro Fujita
Kohzoh Imai
机构
[1] First Department of Internal Medicine,
[2] Sapporo Medical University,undefined
[3] S-1,undefined
[4] W-16,undefined
[5] Chuo-ku,undefined
[6] Sapporo 060-8543,undefined
[7] Japan,undefined
[8] Department of Radiology,undefined
[9] Sapporo Medical University,undefined
[10] S-1,undefined
[11] W-16,undefined
[12] Chuo-ku,undefined
[13] Sapporo 060-8543,undefined
[14] Japan,undefined
[15] Faculty of Pharmaceutical Sciences,undefined
[16] University of Tokyo,undefined
[17] Tokyo,undefined
[18] Japan,undefined
[19] Department of Laboratory Medicine and Pathology,undefined
[20] Sapporo National Hospital,undefined
[21] Sapporo,undefined
[22] Japan,undefined
来源
关键词
Key words: sulfated carbohydrate chain; MUC; Barrett's esophagus; esophageal adenocarcinoma;
D O I
暂无
中图分类号
学科分类号
摘要
Columnar epithelium-lined esophagus (Barrett's esophagus) is an acquired disorder associated with a high incidence of adenocarcinoma of the lower esophagus. Columnar epithelium resembling intestinal metaplasia (IM) is especially important, since it is considered to be a premalignant condition. The aim of this study was to define the sulfated carbohydrate chain of mucin and its core peptide profile in Barrett's esophagus (BE) and to compare it with the profile in Barrett's adenocarcinoma and lower esophageal adenocarcinoma. The sulfated carbohydrate chain was not expressed in 16 specimens of normal esophageal epithelium, but in BE, it was expressed in 50% (8/16) of the specimens. This chain was detected in 100% (7/7) of esophageal adenocarcinoma specimens, including four cases of Barrett's adenocarcinoma. These data suggest that the sulfated carbohydrate chain may be associated with malignant phenotype of the esophagus. MUC1 core peptide was positive in 87% (13/15) of BE specimens and in 29% (2/7) of the esophageal adenocarcinoma specimens. MUC2 core peptide was present in 57% (8/14) and 43% (3/7) of these specimens, respectively. These data suggest that Barrett's epithelium, which is similar to IM, but not normal esophageal epithelium, expresses the sulfated sugar chain which is known to be present in gastric IM and colonic mucosa. However, there was no significant correlation between the expression of the sulfated sugar chain and the expression of either mucin core peptide MUC1 or MUC2. Thus, this carbohydrate chain may be expressed on as yet unidentified core proteins, other than MUC1 or MUC2 core peptide, in BE and esophageal adenocarcinoma. Identification of these proteins may be very important in helping to detect premalignant status in BE.
引用
收藏
页码:811 / 815
页数:4
相关论文
共 50 条
  • [31] Expression profile and cellular localizations of mucin proteins, CK7, and cytoplasmic p27 in Barrett's esophagus and esophageal adenocarcinoma
    Ozcan, H. Ece Arslan
    Anuk, Turgut
    Ozden, Ozkan
    [J]. ADVANCES IN MEDICAL SCIENCES, 2018, 63 (02): : 296 - 300
  • [32] Glutathione S-transferase-Pi expression is downregulated in patients with Barrett's esophagus and esophageal adenocarcinoma
    Brabender, J
    Lord, RV
    Wickramasinghe, K
    Metzer, R
    Schneider, PM
    Park, JM
    Hölscher, AH
    DeMeester, TR
    Danenberg, KD
    Danenberg, PV
    [J]. JOURNAL OF GASTROINTESTINAL SURGERY, 2002, 6 (03) : 359 - 367
  • [33] Glutathione S-transferase-Pi expression is downregulated in patients with Barrett’s esophagus and esophageal adenocarcinoma
    Jan Brabender
    Reginald V. Lord
    Kumari Wickramasinghe
    Ralf Metzger
    Paul M. Schneider
    Ji-Min Park
    Arnulf H. Hölscher
    Tom R. DeMeester
    Kathleen D. Danenberg
    Peter V. Danenberg
    [J]. Journal of Gastrointestinal Surgery, 2002, 6 : 359 - 367
  • [34] Dynamic changes in microRNA expression profiles reflect progression of Barrett's esophagus to esophageal adenocarcinoma
    Slaby, Ondrej
    Srovnal, Josef
    Radova, Lenka
    Gregar, Jan
    Juracek, Jaroslav
    Luzna, Pavla
    Svoboda, Marek
    Hajduch, Marian
    Ehrmann, Jiri
    [J]. CARCINOGENESIS, 2015, 36 (05) : 521 - 527
  • [35] Enhanced PPAR-γ Expression May Correlate With the Development of Barrett's Esophagus and Esophageal Adenocarcinoma
    Wang, Wen
    Wang, Rong
    Zhang, Zhijian
    Li, Dazhou
    Yu, Yinghao
    [J]. ONCOLOGY RESEARCH, 2010, 19 (3-4) : 141 - 147
  • [36] Epithelial PD-L2 Expression Marks Barrett's Esophagus and Esophageal Adenocarcinoma
    Derks, Sarah
    Nason, Katie S.
    Liao, Xiaoyun
    Stachler, Matthew D.
    Liu, Kevin X.
    Bin Liu, Jie
    Sicinska, Ewa
    Goldberg, Michael S.
    Freeman, Gordon J.
    Rodig, Scott J.
    Davison, Jon M.
    Bass, Adam J.
    [J]. CANCER IMMUNOLOGY RESEARCH, 2015, 3 (10) : 1123 - 1129
  • [37] Expression of acidic fibroblast growth factor in Barrett's esophagus and associated esophageal adenocarcinoma - Discussion
    Kaiser, LR
    Soslow, RA
    [J]. JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1997, 114 (05): : 843 - 843
  • [38] Characterization of Sonic Hedgehog expression and Hedgehog pathway activity in Barrett's esophagus and esophageal adenocarcinoma
    Rakhlin, Elena Y.
    Mino-Kenudson, Mari
    Warshaw, Andrew L.
    Thayer, Sarah P.
    [J]. CANCER RESEARCH, 2006, 66 (08)
  • [39] Expression of C1q Complement Component in Barrett's Esophagus and Esophageal Adenocarcinoma
    Bobryshev, Yuri V.
    Lu, Jinhua
    Lord, Reginald V. N.
    [J]. JOURNAL OF GASTROINTESTINAL SURGERY, 2010, 14 (08) : 1207 - 1213
  • [40] MicroRNA Expression Signatures during Malignant Progression from Barrett's Esophagus to Esophageal Adenocarcinoma
    Wu, Xifeng
    Ajani, Jaffer A.
    Gu, Jian
    Chang, David W.
    Tan, Weiqi
    Hildebrandt, Michelle A. T.
    Huang, Maosheng
    Wang, Kenneth K.
    Hawk, Ernest
    [J]. CANCER PREVENTION RESEARCH, 2013, 6 (03) : 196 - 205