High expression of epithelial cellular adhesion molecule in peritoneal metastasis of gastric cancer

被引:0
作者
Motohiro Imano
Tatsuki Itoh
Takao Satou
Atsushi Yasuda
Kohei Nishiki
Hiroaki Kato
Osamu Shiraishi
Ying-Feng Peng
Masayuki Shinkai
Masahiro Tsubaki
Takushi Yasuda
Haruhiko Imamoto
Shozo Nishida
Yoshifumi Takeyama
Hiroshi Furkawa
Kiyokata Okuno
Hitoshi Shiozaki
机构
[1] Kinki University Faculty of Medicine,Department of Surgery
[2] Kinki University Hospital,Cancer Center
[3] Kinki University Faculty of Medicine,Department of Pathology
[4] Kinki University Faculty of Pharmacy,Division of Pharmacotherapy
来源
Targeted Oncology | 2013年 / 8卷
关键词
Gastric cancer; Peritoneal metastasis; Epithelial cellular adhesion molecule (EpCAM); Target therapy;
D O I
暂无
中图分类号
学科分类号
摘要
Intraperitoneally administrated epithelial cellular adhesion molecule (EpCAM) monoclonal antibody is a therapeutic agent in patients with malignant effusion in several types of carcinoma. However, the role of EpCAM in peritoneal metastasis (PM) lesions and primary lesions of gastric cancer (GC) is still unclear. Therefore, in this study, we investigated EpCAM expression in GC patients with PM. We investigated the expression of EpCAM in 35PM lesions and 104 biopsy samples as primary lesions. Immunohistochemical staining was performed using the Ventana Benchmark XT (Roche Diagnostics) system. EpCAM expression was evaluated by calculating the total immunostaining score, which is the product of the proportion score and the intensity score. Overexpression was defined as a total score greater than 4. All PM specimens showed overexpression of EpCAM, and GC cells in both the surface layer and the deep layer of the PM showed a high expression of EpCAM. Meanwhile, in the biopsy sample, the expression of EpCAM ranged from none to strong. The EpCAM score results for PM specimens and biopsy samples were 11.0 ± 2.0 and 6.9 ± 3.9, respectively. The difference between the scores was statistically significant (P < 0.05). The intraperitoneally administrated EpCAM antibody might have a anti-cancer effect in PM lesions of GC. Additionally, it can be assumed that only GC cells which express a high level of EpCAM might metastasize to the peritoneum.
引用
收藏
页码:231 / 235
页数:4
相关论文
共 214 条
  • [1] Corley DA(2001)Oesophageal and gastric cardia adenocarcinomas: analysis of regional variation using the Cancer Incidence in Five Continents database Int J Epidemiol 30 1415-1425
  • [2] Buffler PA(2008)S-1 plus cisplatin versus S-1 alone for first-line treatment of advanced gastric cancer (SPIRITS trial): a phase III trial Lancet Oncol 9 215-221
  • [3] Koizumi W(2000)Peritoneal carcinomatosis from non-gynecologic malignancies: results of the EVOCAPE 1 multicentric prospective study Cancer 88 358-363
  • [4] Narahara H(2005)Adjuvant therapy with edrecolomab versus observation in stage II colon cancer: a multicenter randomized phase III study Onkologie 28 347-350
  • [5] Hara T(2006)Frequent high-level expression of the immunotherapeutic target Ep-CAM in colon, stomach, prostate and lung cancers Br J Cancer 94 128-135
  • [6] Takagane A(2004)Overexpression of epithelial cell adhesion molecule antigen in gallbladder carcinoma is an independent marker for poor survival Clin Cancer Res 10 3131-3136
  • [7] Akiya T(2007)EpCAM (CD326) finding its role in cancer Br J Cancer 96 417-423
  • [8] Takagi M(2010)The trifunctional antibody catumaxomab for the treatment of malignant ascites due to epithelial cancer: results of a prospective randomized phase II/III trial Int J Cancer 127 2209-2221
  • [9] Miyashita K(2010)Catumaxomab: clinical development and future directions MAbs 2 129-136
  • [10] Nishizaki T(2012)A preliminary study of single intraperitoneal administration of paclitaxel followed by sequential systemic chemotherapy with S-1 plus paclitaxel for advanced gastric cancer with peritoneal metastasis Anticancer Res 32 4071-4075